CELL LINE 3M

Abstract

The present invention provides, inter alia, an isolated cell line, 3M as well as methods for making such a cell line and methods of using such a cell line, e.g., to produce a protein such as an immunoglobulin.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This application is a continuation of U.S. patent application Ser. No. 15/485,499, filed Apr. 12, 2017; which is a continuation of U.S. patent application Ser. No. 14/725,561, filed May 29, 2015; which is a continuation of U.S. patent application Ser. No. 13/517,901, filed Jun. 20, 2012; which is the national phase, filed under 35 U.S.C. .sctn. 371, of International Application No. PCT/US2010/060653, filed Dec. 16, 2010; which claims the benefit of U.S. Provisional Patent Application No. 61/289,703, filed Dec. 23, 2009; each of which is herein incorporated by reference in its entirety.

REFERENCE TO SEQUENCE LISTING SUBMITTED ELECTRONICALLY

[0002] The sequence listing of the present application is submitted electronically via EFS-Web as an ASCII formatted sequence listing with a file name "US20097044USCNT-SEQLIST-06MAR2018.TXT", creation date of Mar. 6, 2018, and a size of 62.1 KB. This sequence listing submitted via EFS-Web is part of the specification and is herein incorporated by reference in its entirety.

FIELD OF THE INVENTION

[0003] The field of the invention relates to isolated cells that are useful, e.g., for expression of therapeutic proteins, such as antibodies, as well as to methods of using the cells, for example, to express such proteins.

BACKGROUND OF THE INVENTION

[0004] Production of recombinant proteins suitable for use as therapeutics is typically an arduous and costly process. The expression system to be used to express a given protein is partially dependent upon the protein yield derived from each system. In considering a suitable method for antibody manufacture, for example, a variety of factors must be evaluated. These include antibody structure, the importance of carbohydrate, and expression, which includes yield and productivity, ease of purification and cost of goods. The yield greatly affects the cost of goods associated with any such process.

[0005] In general, recombinant expression technology in mammalian cell culture has been the principal means for the commercial production of therapeutic antibodies. Mammalian systems are beneficial for antibody production for several reasons including the glycosylation pattern on the expressed product. Often the recombinant proteins are produced in mammalian cell culture using either Chinese hamster ovary (CHO) or mouse myeloma (NSO) cell lines.

[0006] Generation of superior cell lines, for recombinant expression, which reach high cell densities and have great longevity in culture produce greater quantities of therapeutic protein per liter of cell culture grown. This leads to a greater efficiency and a lower cost of goods.

SUMMARY OF THE INVENTION

[0007] The present invention provides an isolated Chinese hamster ovary (CHO) cell produced by a method comprising: adapting CHO-DXB11 cells into animal-component free medium in suspension, e.g., for about 83 days; then subcloning the cells into said medium, e.g., twice. In an embodiment of the invention, the subcloning steps comprise (a) serially diluting the adapted cells (e.g., by 1/2 each dilution) in growth medium, for example, in about 100 microliters, e.g., in a microtiter dish comprising, for example, 96 wells; (b) allowing the cells of each dilution to grow; (c) selecting the cells in the highest dilution containing viable cells (e.g., as judged visually, e.g., using a microscope, e.g., to identify the presence of cell colonies); and (d) repeating steps (a), (b) and (c) once more. In an embodiment of the invention, the selected dilution is about 1/64. In an embodiment of the invention, the cell is one that is deposited at the American Type Culture Collection under deposit number PTA-10481. In an embodiment of the invention, the cell is in an aqueous liquid cell culture medium; and/or a vessel such as a vial and/or a freezing medium that contains, e.g., DMSO, e.g., wherein the freezing medium is about 80% serum free medium, about 10% dialyzed fetal bovine serum and about 10% DMSO. Embodiments of the invention include a cell bank or working cell bank comprising the cell. In an embodiment of the invention, the cell comprises a vector which, for example, comprises a polynucleotide encoding one or more proteins such as a light and/or heavy chain immunoglobulin or a fusion protein comprising a polypeptide (e.g., a cytokine or chemokines, e.g., MCP-1) fused to an immunoglobulin (e.g., a Fc) or to human serum albumin. In an embodiment of the invention, the protein encoded by a polynucleotide in the cell is an immunoglobulin comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-8, 21, 22, 42, 43, 58-69, 79, 80, 81, 85, 89, 93 and 101 or a mature fragment thereof or an immunoglobulin comprising one or more CDRs from said immunoglobulin; optionally linked to an immunoglobulin constant chain; or wherein the protein is an immunoglobulin chain comprising:

TABLE-US-00001 (1) CDR-L1: (SEQ ID NO: 9) KASKKVTIFGSISALH, CDR-L2 NGAKLES (20), and CDR-L3: (SEQ ID NO: 11) LQNKEVPYT; (2) CDR-H1: (SEQ ID NO: 12) SYGIT, CDR-H2: (SEQ ID NO: 13) ENYPRSGNTYYNEKFKG, and CDR-H3: (SEQ ID NO: 14) CEFISTVVAPYYYALDY or (SEQ ID NO: 15) SEFISTVVAPYYYALDY or (SEQ ID NO: 16) AEFISTVVAPYYYALDY or (SEQ ID NO: 17) VEFISTVVAPYYYALDY or (SEQ ID NO: 18) SEFISTVMAPYYYALDY or (SEQ ID NO: 19) SEFTSTVVAPYYYALDY; (3) CDRH1: (SEQ ID NO: 23) Gly Phe Thr Phe Ser Ser Tyr Thr Met Ser, CDRH2: (SEQ ID NO: 24) Thr Ile Ser Ser Gly Gly Thr Tyr Thr Tyr Tyr Pro Asp Ser Val Lys Gly, and CDRH3: (SEQ ID NO: 25) Asp Asn His Ala Tyr Asp Arg Gly Pro Phe Phe Asp Tyr; (4) CDRL1: (SEQ ID NO: 26) Lys Ser Ser Gln Asn Leu Phe Tyr Arg Ser Asn Gln Lys Asn His Leu Ala, CDRL2: (SEQ ID NO: 27) Trp Thr Ser Thr Arg Glu Ser, and CDRL3: (SEQ ID NO: 28) Gln Gln Tyr Tyr Ser Tyr Pro Pro Thr; (5) CDRH1: (SEQ ID NO: 29) Ala Tyr Gly Met Asp, CDRH2: (SEQ ID NO: 30) Ser Ile Ser Pro Ser Gly Gly Arg Thr Lys Tyr Ala Asp Ser Val Lys Gly, and CDRH3: (SEQ ID NO: 31) Asp Leu Gly Gly Gly Tyr Tyr Tyr Tyr Tyr Gly Met Asp Val; (6) CDRL1: (SEQ ID NO: 32) Thr Gly Thr Ser Ser Asp Val Gly Gly Tyr Asn Tyr Val Ser, CDRL2: (SEQ ID NO: 33) Glu Val Ser Asn Arg Pro Ser, and CDRL3: (SEQ ID NO: 34) Ser Ser Tyr Thr Ser Ser Ser Thr Leu Phe Tyr Val; (7) CDRH1: (SEQ ID NO: 35) GKTFWSWGIN, CDRH2: (SEQ ID NO: 36) YIYIGTGYTEPNPKYKG, and CDRH3: (SEQ ID NO: 37) IGGYYGNFAD or (SEQ ID NO: 38) IGGYYGNFDQ; (8) CDRL1: (SEQ ID NO: 39) RSSQSLLISGGNTYLN, CDRL2: (SEQ ID NO: 40) LVSKLDQ, and CDRL3: (SEQ ID NO: 41) WQGTYFPLT; (9) CDRH1: (SEQ ID NO: 44) TYWMH or (SEQ ID NO: 45) TYWMH, CDRH2: (SEQ ID NO: 46) EINPTNGHTNYNEKFKS, (SEQ ID NO: 47) EINPTNGHTNYNPSFQG, or (SEQ ID NO: 48) EINPTNGHTNYNQKFQG, and CDRH3: (SEQ ID NO: 49) NYVGSIFDY or (SEQ ID NO: 50) NYVGSIFDY; or (10) CDRL1: (SEQ ID NO: 51) KASENVVSYVS or (SEQ ID NO: 52) KASENVVSYVS, CDRL2: (SEQ ID NO: 53) GASNRNT, (SEQ ID NO: 54) GASNRNT or (SEQ ID NO: 55) GASNRES, and CDRL3: (SEQ ID NO: 56) GQSYNYPYT or (SEQ ID NO: 57) GQSYNYPYT;

optionally linked to an immunoglobulin constant chain.

[0008] The present invention also provides a method for making said cell comprising adapting CHO-DXB11 cells into animal-component free medium in suspension for 83 days; then subcloning the cells into said medium twice.

[0009] The present invention also provides a method for making one or more polypeptides (e.g., an immunoglobulin) comprising introducing one or more polynucleotides encoding said polypeptides into the cell and culturing the cell line in conditions under which the polypeptides are produced; and, optionally, isolating the polypeptide. In an embodiment of the invention, the immunoglobulin an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-8, 21, 22, 42, 43, 58-69, 79, 80, 81, 85, 89, 93 and 101 or a mature fragment thereof or an immunoglobulin comprising one or more CDRs from said immunoglobulin; optionally linked to an immunoglobulin constant chain. In an embodiment of the invention, the immunoglobulin comprises:

TABLE-US-00002 (1) CDR-L1: (SEQ ID NO: 9) KASKKVTIFGSISALH, CDR-L2: (SEQ ID NO: 10) NGAKLES, and CDR-L3: (SEQ ID NO: 11) LQNKEVPYT; (2) CDR-H1: (SEQ ID NO: 12) SYGIT, CDR-H2: (SEQ ID NO: 13) ENYPRSGNTYYNEKFKG, and CDR-H3: (SEQ ID NO: 14) CEFISTVVAPYYYALDY or (SEQ ID NO: 15) SEFISTVVAPYYYALDY or (SEQ ID NO: 16) AEFISTVVAPYYYALDY or (SEQ ID NO: 17) VEFISTVVAPYYYALDY or (SEQ ID NO: 18) SEFISTVMAPYYYALDY or (SEQ ID NO: 19) SEFTSTVVAPYYYALDY; (3) CDRH1: (SEQ ID NO: 23) Gly Phe Thr Phe Ser Ser Tyr Thr Met Ser, CDRH2: (SEQ ID NO: 24) Thr Ile Ser Ser Gly Gly Thr Tyr Thr Tyr Tyr Pro Asp Ser Val Lys Gly, and CDRH3: (SEQ ID NO: 25) Asp Asn His Ala Tyr Asp Arg Gly Pro Phe Phe Asp Tyr; (4) CDRL1: (SEQ ID NO: 26) Lys Ser Ser Gln Asn Leu Phe Tyr Arg Ser Asn Gln Lys Asn His Leu Ala, CDRL2: (SEQ ID NO: 27) Trp Thr Ser Thr Arg Glu Ser, and CDRL3: (SEQ ID NO: 28) Gln Gln Tyr Tyr Ser Tyr Pro Pro Thr; (5) CDRH1: (SEQ ID NO: 29) Ala Tyr Gly Met Asp, CDRH2: (SEQ ID NO: 30) Ser Ile Ser Pro Ser Gly Gly Arg Thr Lys Tyr Ala Asp Ser Val Lys Gly, and CDRH3: (SEQ ID NO: 31) Asp Leu Gly Gly Gly Tyr Tyr Tyr Tyr Tyr Gly Met Asp Val; (6) CDRL1: (SEQ ID NO: 32) Thr Gly Thr Ser Ser Asp Val Gly Gly Tyr Asn Tyr Val Ser, CDRL2: (SEQ ID NO: 33) Glu Val Ser Asn Arg Pro Ser, and CDRL3: (SEQ ID NO: 34) Ser Ser Tyr Thr Ser Ser Ser Thr Leu Phe Tyr Val; (7) CDRH1: (SEQ ID NO: 35) GKTFWSWGIN, CDRH2: (SEQ ID NO: 36) YIYIGTGYTEPNPKYKG, and CDRH3: (SEQ ID NO: 37) IGGYYGNFAD or (SEQ ID NO: 38) IGGYYGNFDQ; (8) CDRL1: (SEQ ID NO: 39) RSSQSLLISGGNTYLN, CDRL2: (SEQ ID NO: 40) LVSKLDQ, and CDRL3: (SEQ ID NO: 41) WQGTYFPLT; (9) CDRH1: (SEQ ID NO: 44) TYWMH or (SEQ ID NO: 45) TYWMH, CDRH2: (SEQ ID NO: 46) EINPTNGHTNYNEKFKS, (SEQ ID NO: 47) EINPTNGHTNYNPSFQG, or (SEQ ID NO: 48) EINPTNGHTNYNQKFQG, and CDRH3: (SEQ ID NO: 49) NYVGSIFDY or (SEQ ID NO: 50) NYVGSIFDY; or (10) CDRL1: (SEQ ID NO: 51) KASENVVSYVS or (SEQ ID NO: 52) KASENVVSYVS, CDRL2: (SEQ ID NO: 53) GASNRNT, (SEQ ID NO: 54) GASNRNT or (SEQ ID NO: 55) GASNRES, and CDRL3: (SEQ ID NO: 56) GQSYNYPYT or (SEQ ID NO: 57) GQSYNYPYT;

optionally linked to an immunoglobulin constant chain. In an embodiment of the invention, the immunoglobulin is a light chain immunoglobulin linked to a kappa or lambda constant immunoglobulin chain and/or wherein the immunoglobulin is a heavy chain immunoglobulin linked to a gamma-1, gamma-2, gamma-3 or gamma-4 constant immunoglobulin chain.

[0010] The present invention also provides a method for producing an antibody comprising inoculating an initial mammalian cell growth medium, pre-warmed to about 37.degree. C.; which initial medium comprises HEPES, sodium bicarbonate buffers, inorganic salts, non-essential amino acids, recombinant human insulin, trace elements and surfactants; and which does not comprise L-glutamine, antibiotics, antimycotics or animal-derived components; with one or more of said cells expressing the antibody light chain immunoglobulin and heavy chain immunoglobulin, to a cell density of about 2.5-5.times.10.sup.5 cells/ml; and, adding the following supplements to the medium before, simultaneously with or immediately after said inoculation:

soy hydrolysate to a final concentration of about 10 g/liter; and, optionally, an amino acid feed wherein the concentration of the components added by said amino acid feed are approximately those set forth below:

[0011] L-arginine: 126.4 mg/liter

[0012] L-cystine: 34 mg/liter

[0013] L-histidine: 42 mg/liter

[0014] L-isoleucine: 52 mg/liter

[0015] L-leucine: 52 mg/liter

[0016] L-lysine: 72 mg/liter

[0017] L-Methionine: 15.2 mg/liter

[0018] L-phenylalanine: 33 mg/liter

[0019] L-threonine: 47.6 mg/liter

[0020] L-tryptophan: 10.2 mg/liter

[0021] L-tyrosine: 36 mg/liter

[0022] L-valine: 46.8 mg/liter

[0023] L-alanine: 8.9 mg/liter

[0024] L-asparagine: 30 mg/liter

[0025] L-aspartic acid: 26.6 mg/liter

[0026] L-glutamic acid: 29.4 mg/liter

[0027] glycine: 15 mg/liter

[0028] L-proline: 23 mg/liter

[0029] L-serine: 21 mg/liter, and, when viable cell density reaches over about 1.2.times.10.sup.6 cells/ml, adding supplement feeds wherein the concentration of the components added by said supplement feeds are approximately those set forth below:

[0030] Sodium selenite: 0.01426 mg/liter

[0031] Adenine sulfate: 1.632 mg/liter

[0032] Adenosine: 17.6 mg/liter

[0033] Cytidine: 17.6 mg/liter

[0034] Guanosine: 17.6 mg/liter

[0035] Uridine: 17.6 mg/liter

[0036] Hypoxanthine: 11.8 mg/liter

[0037] L-citrulline: 12.6 mg/liter

[0038] L-ornithine-HCl: 25.6 mg/liter

[0039] Biotin: 0.28 mg/liter

[0040] Flavin Adenine Dinucleotide: 0.05 mg/liter

[0041] Folic Acid: 4.6 mg/liter

[0042] Lipoic Acid: 0.52 mg/liter

[0043] Niacin: 31.4 mg/liter

[0044] Pyridoxine HCl: 3 mg/liter

[0045] Riboflavin: 1.86 mg/liter

[0046] Thiamine HCl: 16 mg/liter

[0047] Vitamin E: 0.376 mg/liter

[0048] Vitamin B12: 3.4 mg/liter

[0049] Choline Chloride: 50.2 mg/liter

[0050] Ethanolamine HCl: 4.4 mg/liter

[0051] idnositol: 73.2 mg/liter

[0052] Thymidine: 7.8 mg/liter

[0053] Putrescine 2HCl: 0.4 mg/liter

[0054] Progesterone: 0.015 mg/liter

[0055] D-Calcium Pantothenate: 23.8 mg/liter

[0056] L-asparagine: 812 mg/liter

[0057] L-proline 216 mg/liter

[0058] L-isoleucine 370 mg/liter

[0059] L-cysteine-HCl 224 mg/liter

[0060] L-leucine 332 mg/liter

[0061] L-threonine 164 mg/liter

[0062] L-tyrosine 198 mg/liter

[0063] L-arginine 186 mg/liter

[0064] L-aspartic acid 71 mg/liter

[0065] L-glutamic acid 126 mg/liter

[0066] Glycine 57 mg/liter

[0067] L-histidine 125 mg/liter

[0068] L-methionine 132 mg/liter

[0069] L-tryptophan 99 mg/liter

[0070] L-lysine 293 mg/liter

[0071] L-phenylalanine 174 mg/liter

[0072] L-valine 262 mg/liter

[0073] L-serine: 260 mg/liter

[0074] Sodium phosphate monobasic: 288.2 mg/liter

[0075] Zinc sulfate: 1.08 mg/liter

[0076] Cupric sulfate: 0.0032 mg/liter

[0077] Ammonium vanadate: 0.00078 mg/liter

[0078] Cobalt chloride: 0.0025 mg/liter

[0079] Nickel dichloride hexahydrate: 0.0004 mg/liter

[0080] Sodium molybdate dehydrate: 0.00016 mg/liter; and, maintaining glucose concentration in the medium at about 1.5 g/liter and maintaining L-glutamine concentration in the medium at about 150 mg/liter; and during cell growth maintaining O.sub.2 concentration at about 60%; pH at about 6.8.+-.0.02 and temperature at about 36.5.degree. C..+-.0.5.degree. C.; and, optionally, removing the host cells from the medium when cell viability is below about 60%; and, optionally, recovering the culture medium from the cells by disk-stack centrifuging the medium, depth filtering the medium and filtering the medium through a filter with about a 0.2 micron pore size; and/or, optionally, purifying the immunoglobulins from the medium by column chromatographic fractionation.

BRIEF DESCRIPTION OF THE FIGURES

[0081] FIG. 1. Evaluation of Cell Growth Potential for 3M and ISA Host Cells in batch mode.

[0082] FIG. 2. Cell recovery efficiency after transfection for murine anti-IL17 project.

[0083] FIG. 3. Antibody titers after cloning in 96-well for 19 days after transfection for anti-IL23, cyno-anti-TSLP, and anti-HGF projects.

[0084] FIG. 4. Specific productivity of successful clones for anti-IL23 version 2 project.

DETAILED DESCRIPTION OF THE INVENTION

[0085] The present invention provides an isolated Chinese Hamster Ovary (CHO-DXB11) cell for therapeutic antibody production, 3M. 3M cells were deposited, under the Budapest Treaty, on Nov. 17, 2009 with the American Type Culture Collection (ATCC); 10801 University Boulevard; Manassas, Va. 20110-2209. The cells were deposited at the ATCC under deposit number PTA-10481. All restrictions on access to the cells deposited in ATCC will be irrevocably removed upon grant of a patent.

[0086] The present invention also includes derivatives of the cell lines of the present invention. Derivatives include mutants comprising the 3M genetic background for the for the presence of one or more additional genetic mutations, e.g., wherein such derivative cell lines retain the beneficial properties of the parental 3M cell line (e.g., protein production in serum free suspension culture, cell growth and/or clone recovery rate).

[0087] The 3M cell line originated from the well known Chinese Hamster Ovary cell line, CHO-DXB11. CHO DXB11 cells are available from the American Type Culture Collection, e.g., under deposit no. CRL-11397. Briefly, CHO-DXB11 was suspension-adapted for three months followed by two rounds of subsequent cloning in a serum-free protein-free medium. Relative to previously developed and known cell lines, the 3M cell line is robust in cell growth, superior in clone recovery efficiency and produces high antibody titers in suspension mode in serum-free media. 3M has been used to generate highly productive clones for production of several antibodies.

[0088] The present invention includes not only individual isolated 3M cells but also master cell banks (MCB) and working cell banks (WCB), e.g., comprising 3M cells that comprise one or more genes encoding therapeutic proteins to be expressed. Typically, when a cell line is to be used over many manufacturing cycles, a two-tiered cell banking system consisting of a master cell bank or master seed bank and a working cell bank can be established. A cell line is generally established from a single host cell clone and this cell line is used to make-up the MCB. Generally, this MCB must be characterized and extensively tested for contaminants such as bacteria, fungi, viruses and mycoplasma. A sample of cells from the MCB can be expanded to form the WCB, which is characterized for cell viability prior to use in a manufacturing process. The cells in a MCB or WCB can be stored in vials, for example, at low temperature (e.g., 0.degree. C. or lower, -20.degree. C. or -80.degree. C., or in liquid nitrogen, e.g., at -110.degree. C. to -180.degree. C.). Typically, the working cell bank includes cells from one vial of the master bank which have been grown for several passages before storage. In general, when future cells are needed, they are taken from the working cell bank; whereas, the master cell bank is used only when necessary, ensuring a stock of cells with a low passage number to avoid genetic variation within the cell culture.

[0089] Subcloning refers to a progressive dilution of cells in series, e.g., in wells of a 96 well microtiter plate, in predetermined ratios to produce single colonies.

Molecular Biology

[0090] In accordance with the present invention there may be employed conventional molecular biology, microbiology, and recombinant DNA techniques within the skill of the art. Such techniques are explained fully in the literature. See, e.g., Sambrook, Fritsch & Maniatis, Molecular Cloning: A Laboratory Manual, Second Edition (1989) Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (herein "Sambrook, et al., 1989"); DNA Cloning: A Practical Approach, Volumes I and II (D. N. Glover ed. 1985); Oligonucleotide Synthesis (M. J. Gait ed. 1984); Nucleic Acid Hybridization (B. D. Hames & S. J. Higgins eds. (1985)); Transcription And Translation (B. D. Hames & S. J. Higgins, eds. (1984)); Animal Cell Culture (R. I. Freshney, ed. (1986)); Immobilized Cells And Enzymes (IRL Press, (1986)); B. Perbal, A Practical Guide To Molecular Cloning (1984); F. M. Ausubel, et al. (eds.), Current Protocols in Molecular Biology, John Wiley & Sons, Inc. (1994).

[0091] A "polynucleotide", "nucleic acid" or "nucleic acid molecule" DNA and RNA (e.g., mRNA), single or double stranded.

[0092] A "polynucleotide sequence", "nucleic acid sequence" or "nucleotide sequence" is a series of nucleotide bases (also called "nucleotides") in a nucleic acid, such as DNA or RNA, and means any chain of two or more nucleotides.

[0093] A "coding sequence" or a sequence "encoding" an expression product, such as a RNA, polypeptide, protein, or enzyme, is a nucleotide sequence that, when expressed, results in production of the product.

[0094] The term "gene" means a DNA sequence that codes for or corresponds to a particular sequence of ribonucleotides or amino acids which comprise all or part of one or more RNA molecules, proteins or enzymes, and may or may not include regulatory DNA sequences, such as promoter sequences, which determine, for example, the conditions under which the gene is expressed. Genes may be transcribed from DNA to RNA which may or may not be translated into an amino acid sequence.

[0095] A "protein sequence", "peptide sequence" or "polypeptide sequence" or "amino acid sequence" refers to a series of two or more amino acids in a protein, peptide or polypeptide.

[0096] "Protein", "peptide" or "polypeptide" includes a contiguous string of two or more amino acids.

[0097] The terms "isolated polynucleotide" or "isolated polypeptide" include a polynucleotide (e.g., RNA or DNA molecule, or a mixed polymer) or a polypeptide, respectively, which are partially (to any degree) or fully separated from other components that are normally found in cells or in recombinant DNA expression systems. These components include, but are not limited to, cell membranes, cell walls, ribosomes, polymerases, serum components and extraneous genomic sequences.

[0098] An isolated polynucleotide or polypeptide will, in an embodiment of the invention, be an essentially homogeneous composition.

[0099] "Amplification" of DNA as used herein includes the use of polymerase chain reaction (PCR) to increase the concentration of a particular DNA sequence within a mixture of DNA sequences. For a description of PCR see Saiki, et al., Science (1988) 239:487. The term "host cell" includes any cell of any organism (e.g., a CHO cell such as 3M) that is selected, modified, transfected, transformed, grown, or used or manipulated in any way, for the production of a substance by the cell, for example the expression or replication, by the cell, of a gene, a DNA or RNA sequence or a protein. Host cells also include bacterial cells (e.g., E. coli), murine macrophage J774 cells or any other macrophage cell line and human intestinal epithelial Caco2 cells.

[0100] The nucleic acids herein may be flanked by natural regulatory (expression control) sequences, or may be associated with heterologous sequences, including promoters, internal ribosome entry sites (IRES) and other ribosome binding site sequences, enhancers, response elements, suppressors, signal sequences, polyadenylation sequences, introns, 5'- and 3'-non-coding regions, and the like.

[0101] In general, a "promoter" or "promoter sequence" is a DNA regulatory region capable of binding an RNA polymerase in a cell (e.g., directly or through other promoter-bound proteins or substances) and initiating transcription of a coding sequence. A promoter sequence is, in general, bounded at its 3' terminus by the transcription initiation site and extends upstream (5' direction) to include the minimum number of bases or elements necessary to initiate transcription at any level. Within the promoter sequence may be found a transcription initiation site (conveniently defined, for example, by mapping with nuclease S1), as well as protein binding domains (consensus sequences) responsible for the binding of RNA polymerase. The promoter may be operably associated with other expression control sequences, including enhancer and repressor sequences or with a nucleic acid of the invention. Promoters which may be used to control gene expression include, but are not limited to, cytomegalovirus (CMV) promoter (U.S. Pat. Nos. 5,385,839 and 5,168,062), the SV40 early promoter region (Benoist, et al., (1981) Nature 290:304-310), the promoter contained in the 3' long terminal repeat of Rous sarcoma virus (Yamamoto, et al., (1980) Cell 22:787-797), the herpes thymidine kinase promoter (Wagner, et al., (1981) Proc. Natl. Acad. Sci. USA 78:1441-1445), the regulatory sequences of the metallothionein gene (Brinster, et al., (1982) Nature 296:39-42); prokaryotic expression vectors such as the .beta.-lactamase promoter (Villa-Komaroff, et al., (1978) Proc. Natl. Acad. Sci. USA 75:3727-3731), or the tac promoter (DeBoer, et al., (1983) Proc. Natl. Acad. Sci. USA 80:21-25); see also "Useful proteins from recombinant bacteria" in Scientific American (1980) 242:74-94; and promoter elements from yeast or other fungi such as the Gal 4 promoter, the ADC (alcohol dehydrogenase) promoter, PGK (phosphoglycerol kinase) promoter or the alkaline phosphatase promoter.

[0102] A coding sequence is "under the control of", "functionally associated with" or "operably associated with" transcriptional and translational control sequences in a cell when the sequences direct RNA polymerase mediated transcription of the coding sequence into RNA, preferably mRNA, which then may be RNA spliced (if it contains introns) and, optionally, translated into a protein encoded by the coding sequence.

[0103] The terms "express" and "expression" mean allowing or causing the information in a gene, RNA or DNA sequence to become manifest; for example, producing a protein by activating the cellular functions involved in transcription and translation of a corresponding gene. A DNA sequence is expressed in or by a cell to form an "expression product" such as an RNA (e.g., mRNA) or a protein. The expression product itself may also be said to be "expressed" by the cell.

[0104] The term "transformation" means the introduction of a nucleic acid into a cell. The introduced gene or sequence may be called a "clone". A host cell that receives the introduced DNA or RNA has been "transformed" and is a "transformant" or a "clone." The DNA or RNA introduced to a host cell can come from any source, including cells of the same genus or species as the host cell, or from cells of a different genus or species.

[0105] The term "vector" includes a vehicle (e.g., a plasmid) by which a DNA or RNA sequence can be introduced into a host cell, so as to transform the host and, optionally, promote expression and/or replication of the introduced sequence.

[0106] Vectors that can be used in this invention include plasmids, viruses, bacteriophage, integratable DNA fragments, and other vehicles that may facilitate introduction of the nucleic acids into the genome of the host. Plasmids are the most commonly used form of vector but all other forms of vectors which serve a similar function and which are, or become, known in the art are suitable for use herein. See, e.g., Pouwels, et al., Cloning Vectors: A Laboratory Manual, 1985 and Supplements, Elsevier, N.Y., and Rodriguez et al. (eds.), Vectors: A Survey of Molecular Cloning Vectors and Their Uses, 1988, Buttersworth, Boston, Mass.

[0107] The term "expression system" means a host cell (e.g., a 3M cell) and compatible vector which, under suitable conditions, can express a protein or nucleic acid which is carried by the vector and introduced to the host cell.

[0108] Mutant CHO cells comprising the 3M cell genetic background are also within the scope of the present invention. Such mutant cells are identical to a 3M cell of the present invention but for the presence of one or more additional genetic mutations. Genetic mutations can take the form of gene knock-outs, deletions, point mutations, etc. Accordingly, the present invention includes methods for generating a 3M cell line mutant comprising adapting CHO-DXB11 cells into animal-component free medium in suspension for 83 days; then subcloning the cells into said medium twice, then introducing one or more genetic mutations into such cells. Cells produced by such a method are also within the scope of the present invention. Methods for introducing genetic mutations into CHO cells are within the ability of any practitioner of ordinary skill in the art. For example, mutations may be introduced by way of chemical or radiation mutagenesis (e.g., using ethyl methanesulfonate (EMS) treatment, N-methyl-N-nitro-N-nitrosoguanidine (NG) treatment, ultraviolet (UV) light treatment, gamma irradiation, X-ray irradiation, fast neutron irradiation) or homologous recombination based methods for introducing mutations (e.g., site-directed mutagenesis, for example PCR-based introduction of a specific point mutation or recombinant knock out or knock-in of a given gene or locus). Chromosomal locations into which mutations may be introduced may be selected from those appearing in the public sequence databases.

3M Cells

[0109] The present invention includes an isolated Chinese hamster ovary cell, the "3M" cell, the exhibits superior properties allowing efficient production of various polypeptides. An embodiment of the 3M cells of the present invention were deposited, under the Budapest Treaty, on Nov. 17, 2009 with the American Type Culture Collection (ATCC); 10801 University Boulevard; Manassas, Va. 20110-2209. The cells were deposited at the ATCC under deposit number PTA-10481. All restrictions on access to the cells deposited in ATCC will be irrevocably removed upon grant of a patent. 3M cells may be produced by method comprising adapting CHO-DXB11 cells into animal-component free medium in suspension for about 3 months (e.g., about 83 days or about 80-90 days or about 90 days); then subcloning the cells into said medium twice.

[0110] Subcloning can be performed by a method comprising the steps of

(a) serially diluting the adapted cells in serum-free growth medium (e.g., any of those discussed herein), for example, animal component-free medium; e.g., wherein the cells are diluted by 1/2 each time. e.g., wherein the serial dilutions are done in a low volume of about 100 microliters. e.g., wherein the serial dilutions are done in the wells of a 96 well microtiter plate. (b) allowing the cells of each dilution to grow; e.g., wherein the cells are allowed to grow for about 2 weeks e.g., wherein the cells are allowed to grow in high humidity and/or 7.5% CO.sub.2. e.g., wherein the cells are allowed to grow at 37.degree. C. (c) selecting the cells in the highest dilution (i.e., lowest concentration of cells) containing viable cells; e.g., wherein the cells in a dilution are determined to be viable upon visual inspection e.g., using a microscope wherein cellular colonies are observed. e.g., wherein the highest dilution is about 1/64. e.g., wherein cells that are selected are transferred into a higher volume (e.g., about 2 ml of medium, e.g., in a T-25 flask) of serum free growth medium and allowed to grow (e.g., shaking at about 70 rpm e.g., for about 1 week, e.g., at about 37.degree. C., e.g., at about 7.5% CO.sub.2) before proceeding to step (d) and then re-serially diluting the cells. and (d) repeating steps (a), (b) and (c) once more.

Proteins

[0111] The present invention includes embodiments comprising methods for recombinantly producing proteins, such as immunoglobulin chains or therapeutic proteins, in the 3M cells. Such immunoglobulin chains include the light and/or heavy immunoglobulin chains for the following antibodies: anti-IL23 (e.g., anti-p19), anti-PD1, anti-TSLP, anti-HGF, anti-IL17, anti-IL23 Receptor, anti-BTLA, cyno-anti-TSLP (cynomolgus frameworks and Ig constant domain, specific for cynomologous monkey TSLP) as well as sB4-HSA (HAS is human serum albumin), mouse Embrel (soluble mouse TNF receptor linked to a mouse Fc portion of an IgG1), and cTLA4-IgG. Such methods are discussed in detail herein. In an embodiment of the invention, the immunoglobulin forms part of an antibody (e.g., human antibody, humanized antibody, chimeric antibody) or antigen-binding fragment thereof, e.g., including an immunoglobulin light and/or heavy chain variable region, optionally linked with an immunoglobulin constant region.

[0112] For example, the present invention includes methods wherein a protein to be expressed in a 3M cell (e.g., a light chain and/or heavy chain immunoglobulin) is encoded by a polynucleotide in a plasmid vector, e.g., wherein the polynucleotide is operably linked to a promoter such as a CMV promoter. In an embodiment of the invention, the light and heavy chains are included in a single plasmid vector or in two separate plasmid vectors.

[0113] In an embodiment of the invention, the immunoglobulin chain encodes any of those set forth below; for example, any of the following immunoglobulin light and/or heavy chains and/or any of the CDRs thereof (e.g., all 3 from a single light or heavy chain).

[0114] Dotted, underscored type encodes the signal peptide. Solid underscored type encodes the CDRs. Plain type encodes the framework regions. In an embodiment of the invention, the chains are expressed with the signal peptide which is cleaved upon secretion from the host cell to generate a mature fragment of the chain.

[0115] The present invention also comprises compositions including 3M cells in the presence of heavy and/or light immunoglobulin chains and/or antibodies comprising the chain(s) or antigen-binding fragments thereof, e.g., which are in a liquid cell growth culture medium, e.g., wherein such chains were secreted from a host cell (e.g., 3M).

[0116] Processes for producing any of the following immunoglobulin polypeptide chains comprising any of the following amino acid sequences or mature fragments thereof or antibodies or antigen-binding fragments thereof comprising such chains or fragments in 3M cells form part of the present invention along with 3M cells themselves comprising the polypeptides and/or polynucleotides encoding said polypeptides (e.g., in a vector). In an embodiment of the invention, the protein is a light or heavy chain immunoglobulin variable chain (either mature (lacking the secretion signal) or unprocessed), optionally linked to an immunoglobulin heavy or light constant chain immunoglobulin, e.g., wherein the variable region comprises an amino acid sequence set forth below, or a mature fragment thereof or wherein the immunoglobulin comprises one or more CDRs (e.g., 3 light chain CDRs or 3 heavy chain CDRs) from those set forth herein:

TABLE-US-00003 19D12/15H12 Light Chain (SEQ ID NO: 1) ##STR00001## QSPKLLIKYASQSLSGVPSRFSGSGSGTDFTLTINSLEAEDAAAYYCHQSSRLPHTFGGG TKVEIKRT 19D12/15H12 Heavy Chain (SEQ ID NO: 2) ##STR00002## GKGLEWISVIDTRGATYYADSVKGRFTISRDNAKNSLYLQMNSLRAEDMAVYYCARLGNF YYGMDVWGQGTTVTVSS 19D12/15H12 Light Chain-C (LCC) (SEQ ID NO: 3) ##STR00003## G E R V T I T C R A S Q S I G S S L H W Y Q Q K P G Q S P K L L I K Y A S Q S L S G V P S R F S G S G S G T D F T L T I S S L E A E D A A A Y Y C H Q S S R L P H T F G Q G T K V E I K R T 19D12/15H12 Light Chain-D (LCD) (SEQ ID NO: 4) ##STR00004## G E R V T I T C R A S Q S I G S S L H W Y Q Q K P G Q S P K L L I K Y A S Q S L S G V P S R F S G S G S G T D F T L T I S S L E A E D F A V Y Y C H Q S S R L P H T F G Q G T K V E I K R T 19D12/15H12 Light Chain-E (LCE) (SEQ ID NO: 5) ##STR00005## G E R A T L S C R A S Q S I G S S L H W Y Q Q K P G Q A P R L L I K Y A S Q S L S G I P D R F S G S G S G T D F T L T I S R L E P E D A A A Y Y C H Q S S R L P H T F G Q G T K V E I K R T 19D12/15H12 Light Chain-F (LCF) (SEQ ID NO: 6) ##STR00006## G E R A T L S C R A S Q S I G S S L H W Y Q Q K P G Q A P R L L I K Y A S Q S L S G I P D R F S G S G S G T D F T L T I S R L E P E D F A V Y Y C H Q S S R L P H T F G Q G T K V E I K R T 19D12/15H12 heavy chain-A (HCA) (SEQ ID NO: 7) ##STR00007## Gly Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser Phe Ala Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Ile Ser Val Ile Asp Thr Arg Gly Ala Thr Tyr Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser Leu Tyr Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Ala Arg Leu Gly Asn Phe Tyr Tyr Gly Met Asp Val Trp Gly Gln Gly Thr Thr Val Thr Val Ser Ser 19D12/15H12 heavy chain-B (HCB) (SEQ ID NO: 8) ##STR00008## Gly Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser Phe Ala Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Ile Ser Val Ile Asp Thr Arg Gly Ala Thr Tyr Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser Leu Tyr Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Ala Arg Leu Gly Asn Phe Tyr Tyr Gly Met Asp Val Trp Gly Gln Gly Thr Thr Val Thr Val Ser Ser

[0117] See international application publication no. WO2003/100008 which is incorporated herein by reference in its entirety.

[0118] Other variable heavy and light chain immunoglobulins that can form part of an anti-IGF1R antibody and antigen-binding fragment thereof are as follows:

TABLE-US-00004 V.sub.H domains (1) EVQLVQSGGGLVHPGGSLRLSCAGS GFTFRNYAMY WVRQAPGKGLEWVS AIG-SGGGTYYADSVKG (2) QVELVESGGGVVQPGRSQRLSCAAS GFTFSSYGMH WVRQAPGKGLEWVA IIWFDGSSTYYADSVRG (3) EVQLLESGGGLVQPGGSLRLSCTAS GFTFSSYAMN WVRQAPGKGLEWVS AISGSGGTTFYADSVKG (4) EVQLVQSGAEVKKPGSSVKVSCKAS GGTFSSYAIS WVRQAPGQGLEWMG GIIPIFGTANYAQKFQG (5) QVQLQESGPGLVKPSGTLSLTCAVS GGSISSSNWWS WVRQPPGKGLEWIG EIY-HSGSTNYNPSLKS (6) QVQLQESGPGLVKPSETLSLTCTVS GYSISGGYLWN WIRQPPGKGLEWIG YIS-YDGTNNYKPSLKD (1) RFTISRDNAKNSLYLQMNSLRAEDMAVYYCAR APNWGSDA----------FDI WGQGTMVTVSS (2) RFTISRDNSKNTLYLQMNSLRAEDTAVYFCAR ELGRR------------YFDL WGRGTLVSVSS (3) RFTISRDNSRTTLYLQMNSLRAEDTAVYYCAK DLGWSDS-----YYYYYGMDV WGQGTTVTVSS (4) RVTITADKSTSTAYMELSSLRSEDTAVYYCAR APLRFLEWSTQDHYYYYYMDV WGKGTTVTVSS (5) RVTISVDKSKNQFSLKLSSVTAADTAVYYCAR WTGRTD-----------AFDI WGQGTWVTVSS (6) RVTISVDTSKNQFSLKLSSVTAADTAVYYCAR YGRV-------------FFDY WGQGTLVTVSS 1 = SEQ ID NO: 58 2 = SEQ ID NO: 60 3 = SEQ ID NO: 62 4 = SEQ ID NO: 64 5 = SEQ ID NO: 66 6 = SEQ ID NO: 68 V.sub.L Domains (a) DIQMTQSPSSLSASVGDRVTITC RASQGISSWLA WYQQKPEKAPKSLIY AASSLQS (b) EIVLTQSPATLSLSPGERATLSC RASQSVSSYLA WYQQKPGQAPRLLIY DASKRAT (c) DIQMTQFPSSLSASVGDRVTITC RASQGIRNDLG WYQQKPGKAPKRLIY AASRLHR (d) SSELTQDP-AVSVALGQTVRITC QGDSLRSYYAT WYQQKPGQAPILVIY GENKRPS (e) DVVMTQSPLSLPVTPGEPASISC RSSQSLLHSNGYNYLD WYLQKPGQSPQLLIY LGSNRAS (f) DIVMTQSPLSLPVTPGEPASISC RSSQSIVHSNGNTYLQ WYLQKPGQSPQLLIY KVSNRLY (a) GVPSRFSGSGSGTDFTLTISSLQPEDFATYYC QQYNSYPPT FGPGTKVDIK (b) GIPARFSGSGSGTDFTLTISSLEPEDFAVYYC QQRSKWPPWT FGQGTKVESK (c) GVPSRFSGSGSGTEFTLTISSLQPEDFATYYC LQHNSYPCS FGQGTKLEIKRT (d) GIPDRFSGSSSGNTASLTITGAQAEDEADYYC KSRDGSGQHLV FGGGTKLTVLG (e) GVPDRFSGSGSGTDFTLKISRVEAEDVGVYYC MQGTHWPLT FGQGTKVEIK (f) GVPDRFSGSGSGTDFTLKISRVEAEDVGVYYC FQGSHVPWT FGQGTKVEIK a = SEQ ID NO: 59 b = SEQ ID NO: 61 c = SEQ ID NO: 63 d = SEQ ID NO: 65 e = SEQ ID NO: 67 f = SEQ ID NO: 69

[0119] In an embodiment of the invention, V.sub.H1 is paired, in an antibody or antigen-binding fragment thereof, with V.sub.La; V.sub.H2 is paired, in an antibody or antigen-binding fragment thereof, with V.sub.Lb; V.sub.H3 is paired, in an antibody or antigen-binding fragment thereof, with V.sub.Lc; V.sub.H4 is paired, in an antibody or antigen-binding fragment thereof, with V.sub.Ld; V.sub.H5 is paired, in an antibody or antigen-binding fragment thereof, with V.sub.Le; and/or V.sub.H6 is paired, in an antibody or antigen-binding fragment thereof, with V.sub.Lf.

[0120] Embodiments of the invention include those wherein the immunoglobulin is expressed in 3M cells, for example, in combination of any of those set forth herein (e.g., LCC and HCA; or LCF and HCA; or LCC and HCB). Pairing of the light and heavy chains can result in generation of an antibody or antigen-binding fragment thereof.

[0121] In an embodiment of the invention, the polypeptide is one or more immunoglobulin chains that can form an anti-IGF1R antibody or antigen-binding fragment thereof that comprises the light and/or heavy chain immunoglobulins set forth below, or variable regions thereof, or chains that comprise the 3 light chain CDRs and/or 3 heavy chain CDRs that, in an embodiment of the invention, are underscored in the sequences set forth below, e.g., wherein the antibody or fragment comprises the two light and two heavy chain immunoglobulins set forth below:

TABLE-US-00005 LIGHT CHAIN (1) (SEQ ID NO: 79) 1 DIVMTQSPLS LPVTPGEPAS ISCRSSQSIV HSNGNTYLQW YLQKPGQSPQ 51 LLIYKVSNRL YGVPDRFSGS GSGTDFTLKI SRVEAEDVGV YYCFQGSHVP 101 WTFGQGTKVE IKRTVAAPSV FIFPPSDEQL KSGTASVVCL LNNFYPREAK 151 VQWKVDNALQ SGNSQESVTE QDSKDSTYSL SSTLTLSKAD YEKHKVYACE 201 VTHQGLSSPV TKSFNRGEC HEAVY CHAIN (2) (SEQ ID NO: 80) 1 QVQLQESGPG LVKPSETLSL TCTVSGYSIT GGYLWNWIRQ PPGKGLEWIG 51 YISYDGTNNY KPSLKDRVTI SRDTSKNQFS LKLSSVTAAD TAVYYCARYG 101 RVFFDYWGQG TLVTVSSAST KGPSVFPLAP SSKSTSGGTA ALGCLVKDYF 151 PEPVTVSWNS GALTSGVHTF PAVLQSSGLY SLSSVVTVPS SSLGTQTYIC 201 NVNHKPSNTK VDKRVEPKSC DKTHTCPPCP APELLGGPSV FLFPPKPKDT 251 LMISRTPEVT CVVVDVSHED PEVKFNWYVD GVEVHNAKTK PREEQYNSTY 301 RVVSVLTVLH QDWLNGKEYK CKVSNKALPA PIEKTISKAK GQPREPQVYT 351 LPPSREEMTK NQVSLTCLVK GFYPSDIAVE WESNGQPENN YKTTPPVLDS 401 DGSFFLYSKL TVDKSRWQQG NVFSCSVMHE ALHNHYTQKS LSLSPGK HEAVY CHAIN (3) 1 QVQLQESGPG LVKPSETLSL TCTVSGYSIT GGYLWNWIRQ PPGKGLEWIG 51 YISYDGTNNY KPSLKDRVTI SRDTSKNQFS LKLSSVTAAD TAVYYCARYG 101 RVFFDYWGQG TLVTVSSAST KGPSVFPLAP SSKSTSGGTA ALGCLVKDYF 151 PEPVTVSWNS GALTSGVHTF PAVLQSSGLY SLSSVVTVPS SSLGTQTYIC 201 NVNHKPSNTK VDKRVEPKSC DKTHTCPPCP APELLGGPSV FLFPPKPKDT 251 LMISRTPEVT CVVVDVSHED PEVKFNWYVD GVEVHNAKTK PREEQYNSTY 301 RVVSVLTVLH QDWLNGKEYK CKVSNKALPA PIEKTISKAK GQPREPQVYT 351 LPPSREEMTK NQVSLTCLVK GFYPSDIAVE WESNGQPENN YKTTPPVLDS 401 DGSFFLYSKL TVDKSRWQQG NVFSCSVMHE ALHNHYTQKS LSLSPGK LIGHT CHAIN (4) 1 DIVMTQSPLS LPVTPGEPAS ISCRSSQSIV HSNGNTYLQW YLQKPGQSPQ 51 LLIYKVSNRL YGVPDRFSGS GSGTDFTLKI SRVEAEDVGV YYCFQGSHVP 101 WTFGQGTKVE IKRTVAAPSV FIFPPSDEQL KSGTASVVCL LNNFYPREAK 151 VQWKVDNALQ SGNSQESVTE QDSKDSTYSL SSTLTLSKAD YEKHKVYACE 201 VTHQGLSSPV TKSFNRGEC

[0122] In an embodiment of the invention, the light and heavy chains of the anti-IGF1R antibody or antigen-binding fragment thereof comprise one or more disulfide bridges arranged as follows:

TABLE-US-00006 DISULFIDE BRIDGES (CHAIN NUMBER:AMINO ACID NUMBER) 1:23 to 1:93 1:139 to 1:199 1:219 to 2:220 2:22 to 2:96 2:144 to 2:200 2:261 to 2:321 2:367 to 2:425 2:226 to 3:226 2:229 to 3:229 3:22 to 3:96 3:144 to 3:200 3:261 to 3:321 3:367 to 3:425 3:220 to 4:219 4:23 to 4:93 4:139 to 4:199

[0123] In an embodiment of the invention, an immunoglobulin chain that can form anti-IL-23 antibody or antigen-binding fragment thereof that comprises 3 light and/or 3 heavy chain CDRs is selected from:

TABLE-US-00007 CDR-L1: (SEQ ID NO: 9) KASKKVTIFGSISALH; CDR-L2: (SEQ ID NO: 10) NGAKLES; and CDR-L3: (SEQ ID NO: 11) LQNKEVPYT; or CDR-H1: (SEQ ID NO: 12) SYGIT; CDR-H2: (SEQ ID NO: 13) ENYPRSGNTYYNEKFKG; and CDR-H3: (SEQ ID NO: 14) CEFISTVVAPYYYALDY or (SEQ ID NO: 15) SEFISTVVAPYYYALDY or (SEQ ID NO: 16) AEFISTVVAPYYYALDY or (SEQ ID NO: 17) VEFISTVVAPYYYALDY or (SEQ ID NO: 18) SEFISTVMAPYYYALDY or (SEQ ID NO: 19) SEFTSTVVAPYYYALDY

[0124] In an embodiment of the invention, an immunoglobulin chain that can form part of an anti-IL-23 p19 antibody or antigen-binding fragment thereof comprises an amino acid sequence selected from:

TABLE-US-00008 Light chain: (SEQ ID NO: 20) DIQMTQSPSSLSASVGDRVTITCRTSENIYSYLAWYQQKPGKAPKLLIYN AKTLAEGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQHHYGIPFTFGQ GTKVEIKR; Heavy chain: (SEQ ID NO: 21) QVQLVQSGAEVKKPGASVKVSCKASGYIFITYWMTWVRQAPGQGLEWMGQ IFPASGSADYNEMFEGRVTMTTDTSTSTAYMELRSLRSDDTAVYYCARGG GGFAYWGQGTLVTVSS; and Heavy chain: (SEQ ID NO: 22) QVQLVQSGAEVKKPGASVKVSCKASGYIFITYWMTWVRQAPGQGLEWMGQ IFPASGSADYAQKLQGRVTMTTDTSTSTAYMELRSLRSDDTAVYYCARGG GGFAYWGQGTLVTVSS.

[0125] In an embodiment of the invention, the immunoglobulin comprises 3 heavy and/or 3 light chain CDRs taken from the immunoglobulin chains discussed above.

[0126] In an embodiment of the invention, an immunoglobulin that can form part of an anti-IL23 p19 antibody or antigen-binding fragment thereof comprises the following CDRs:

TABLE-US-00009 CDRH1: (SEQ ID NO: 23) Gly Phe Thr Phe Ser Ser Tyr Thr Met Ser; CDRH2: (SEQ ID NO: 24) Thr Ile Ser Ser Gly Gly Thr Tyr Thr Tyr Tyr Pro Asp Ser Val Lys Gly; and CDRH3: (SEQ ID NO: 25) Asp Asn His Ala Tyr Asp Arg Gly Pro Phe Phe Asp Tyr; or CDRL1: (SEQ ID NO: 26) Lys Ser Ser Gln Asn Leu Phe Tyr Arg Ser Asn Gln Lys Asn His Leu Ala; CDRL2: (SEQ ID NO: 27) Trp Thr Ser Thr Arg Glu Ser; and CDRL3: (SEQ ID NO: 28) Gln Gln Tyr Tyr Ser Tyr Pro Pro Thr.

[0127] In an embodiment of the invention, an immunoglobulin that can form part of an anti-IL23 p19 antibody or antigen-binding fragment thereof comprises the following CDRs:

TABLE-US-00010 CDRH1: (SEQ ID NO: 29) Ala Tyr Gly Met Asp; CDRH2: (SEQ ID NO: 30) Ser Ile Ser Pro Ser Gly Gly Arg Thr Lys Tyr Ala Asp Ser Val Lys Gly; and CDRH3: (SEQ ID NO: 31) Asp Leu Gly Gly Gly Tyr Tyr Tyr Tyr Tyr Gly Met Asp Val; or CDRL1: (SEQ ID NO: 32) Thr Gly Thr Ser Ser Asp Val Gly Gly Tyr Asn Tyr Val Ser; CDRL2: (SEQ ID NO: 33) Glu Val Ser Asn Arg Pro Ser; and CDRL3: (SEQ ID NO: 34) Ser Ser Tyr Thr Ser Ser Ser Thr Leu Phe Tyr Val.

[0128] In an embodiment of the invention, an immunoglobulin that can form part of an anti-IL23 p19 antibody or antigen-binding fragment thereof comprises the following CDRs:

TABLE-US-00011 CDRH1: (SEQ ID NO: 35) GKTFWSWGIN; CDRH2: (SEQ ID NO: 36) YIYIGTGYTEPNPKYKG; and CDRH3: (SEQ ID NO: 37) IGGYYGNFAD or (SEQ ID NO: 38) IGGYYGNFDQ; or CDRL1: (SEQ ID NO: 39) RSSQSLLISGGNTYLN; CDRL2: (SEQ ID NO: 40) LVSKLDQ; and CDRL3: (SEQ ID NO: 41) WQGTYFPLT.

[0129] In an embodiment of the invention, an immunoglobulin can form part of an anti-IL23 p19 antibody or antigen-binding fragment thereof comprises any of the immunoglobulins, variable regions thereof or CDRs thereof which are set forth in any of U.S. Pat. No. 7,247,711 or U.S. Pat. No. 7,491,391; published U.S. application no. US 2007/0218064; or US 2008/0095775; or published PCT application no. WO 2007/024846.

[0130] For example, in an embodiment of the invention, an immunoglobulin that can form part of an anti-IL-17 antibody or antigen-binding fragment thereof comprises a heavy and/or light chain immunoglobulin that is selected from those below; or an immunoglobulin chain that can form part of an anti-IL-17 antibody or antigen-binding fragment thereof comprises 3 light and/or 3 heavy chain CDRs from any of the chains set forth below:

TABLE-US-00012 Light chain: (SEQ ID NO: 42) DIVMTQSPLSLPVTPGEPASISCKSSQSLLFSENQKNYLAWYLQKPGQSP QLLIYWTSTRQSGVPDRFSGSGSGTDFTLKISRVEAEDVGVYYCQQSYYT PYTFGQGTKVEIKR; and Heavy chain: (SEQ ID NO: 43) QVQLQESGPGLVKPSETLSLTCTVSGFSLPSHSVSWIRQPPGKGLEWIGI IWNQGGTDYNSAFKSRVTISVDTSKNQFSLKLSSVTAADTAVYYCARNAY ITDYYYENYFMDAWGQGTLVTVSS.

[0131] In an embodiment of the invention, an immunoglobulin that can form part of an anti-HGF antibody or antigen-binding fragment thereof comprises the following 3 light and/or 3 heavy chain CDRs

TABLE-US-00013 Heavy Chain CDR1 a (SEQ ID NO: 44) TYWMH b and c (SEQ ID NO: 45) TYWMH; Heavy Chain CDR2 a (SEQ ID NO: 46) EINPTNGHTNYNEKFKS b (SEQ ID NO: 47) EINPTNGHTNYNPSFQG c (SEQ ID NO: 48) EINPTNGHTNYNQKFQG; and Heavy Chain CDR3 a (SEQ ID NO: 49) NYVGSIFDY b and c (SEQ ID NO: 50) NYVGSIFDY; or Light (Kappa) Chain CDR1 a (SEQ ID NO: 51) KASENVVSYVS b and c (SEQ ID NO: 52) KASENVVSYVS; Light (Kappa) Chain CDR2 a (SEQ ID NO: 53) GASNRNT b (SEQ ID NO: 54) GASNRNT c (SEQ ID NO: 55) GASNRES; and Light (Kappa) Chain CDR3 a (SEQ ID NO: 56) GQSYNYPYT b and c (SEQ ID NO: 57) GQSYNYPYT.

[0132] In an embodiment of the invention, the protein is a light or heavy chain immunoglobulin variable chain (either mature (lacking the secretion signal) or unprocessed), optionally linked to an immunoglobulin heavy or light constant chain immunoglobulin, e.g., wherein the variable region comprises an amino acid sequence set forth below, or a mature fragment thereof or wherein the immunoglobulin comprises one or more CDRs (e.g., 3 light chain CDRs or 3 heavy chain CDRs) from those set forth herein (CDRs are underscored):

TABLE-US-00014 XPA.10.064 light chain (SEQ ID NO: 70) SYVLTQPPSASGTPGQRVTISCSGSSSNIGINYVYWYQQLPGTAPKLLIY RNDQRPSGVPDRFSGSKSGTSASLAISGLRSEDEADYYCATWDDSLSGVV FGGGTKVTVL; XPA.10.064.03 heavy chain (SEQ ID NO: 71) EVQLVQSGAEVRKPGASVKVSCKASGYSFTGHYIHWVRQAPGQGLEWMGW INPYSGGTNFPREFQGRVTMTRDTSVNTVYMELTRLTSDDTSVYYCARDQ MVHGGLDYWGQGTLVTVSS; XPA.10.064.04 heavy chain (SEQ ID NO: 72) EVQLVQSGAEVRKPGASVKVSCKASGYSFTGHYIHWVRQAPGQGLEWMGW INPYSGGTNFPREFQGRVTMTRDTSVNTVYMELTRLTSDDTSVYYCARDE MQNGGLDYWGQGTLVTVSS; XPA.10.064.06 heavy chain (SEQ ID NO: 73) EVQLVQSGAEVRKPGASVKVSCKASGYSFTGHYIHWVRQAPGQGLEWMGW INPYSGGTNFPREFQGRVTMTRDTSVNTVYMELTRLTSDDTSVYYCARDE MTRGGLDYWGQGTLVTVSS; XPA.10.064.07 heavy chain (SEQ ID NO: 74) EVQLVQSGAEVRKPGASVKVSCKASGYSFTGHYIHWVRQAPGQGLEWMGW INPYSGGTNFPREFQGRVTMTRDTSVNTVYMELTRLTSDDTSVYYCARDE MHVGGLDYWGQGTLVTVSS; XPA.10.064.10 heavy chain (SEQ ID NO: 75) EVQLVQSGAEVRKPGASVKVSCKASGYSFTGHYIHWVRQAPGQGLEWMGW INPYSGGTNFPREFQGRVTMTRDTSVNTVYMELTRLTSDDTSVYYCARDE MVWGGLDYWGQGTLVTVSS.

[0133] In an embodiment of the invention, the light chain immunoglobulin is fused to an immunoglobulin constant chain, e.g., a kappa chain or a lambda chain. In an embodiment of the invention, the heavy chain immunoglobulin is fused to an immunoglobulin constant chain, e.g., a gamma-1, gamma-2, gamma-3 or gamma-4 chain.

[0134] Other proteins of interest that may be expressed using the methods and 3M cells of the present invention include receptors, ligands, cytokines, chemokines, growth factors, hormones and enzymes.

[0135] For example, in a embodiment of the invention, the 3M cell is used to express mature processed or immature, unprocessed MCP1 (e.g., human MCP1) fused to an immunoglobulin gene (e.g., gamma-1, 2, 3 or 4). In an embodiment of the invention, MCP1 is fused to the immunoglobulin by a peptide linker. In an embodiment of the invention, an unprocessed polypeptide sequence of human MCP1 comprises the following amino acid sequence: MKVSAALLCLLLIAATFIPQGLAQPDAINAPVTCCYNFTNRKISVQRLASYRRITSSKCPKEA- VIFK TIVAKEICADPKQKWVQDSMDHLDKQTQTPKT (SEQ ID NO: 76). In an embodiment of the invention, a mature polypeptide sequence of human MCP1 comprises the following amino acid sequence: QPDAINAPVTCCYNFTNRKISVQRLASYRRITSSKCPKEAVIFKTIVAKEICADPKQKWVQDSMDHL DKQTQTPKT (SEQ ID NO: 77). In an embodiment of the invention, the immunoglobulin is mature polypeptide sequence of human immunoglobulin heavy chain constant region (hinge to CH3 only), isotype .gamma.1 monomeric variant (C to S mutations in the hinge underscored)

TABLE-US-00015 (SEQ ID NO: 78) VEPKSSDKTHTSPPSPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVV VDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQD WLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSRDELTKN QVSLTCLVKGFYPSDTAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKL TVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK.

[0136] For example, in an embodiment of the invention, an immunoglobulin that can form part of an anti-PCSK9 antibody (e.g., AX132, AX189 or 1462/1282) or antigen-binding fragment thereof comprises a heavy and/or light chain immunoglobulin that is selected from those below; or an immunoglobulin chain that can form part of an anti-PCSK9 antibody or antigen-binding fragment thereof comprises 3 light and/or 3 heavy chain CDRs from any of the chains set forth below:

TABLE-US-00016 AX132 VH amino acid sequence: (SEQ ID NO: 81) EVQLLESGGGLVQPGGSLRLSCKASGYTFSSYGMYWVRQAPGKGLEWIG WIDPGSGGTKYNEKFKGKATISRDNSKNTLYLQMNSLRAEDTAVYYCAR ERYGYYFDYWGQGTLVTVSS

e.g., wherein the heavy chain comprises the CDRs:

TABLE-US-00017 AX132 HCDR1 (SEQ ID NO: 82) GYTFSSYGMY AX132 HCDR2 (SEQ ID NO: 83) WIDPGSGGTKYNEKFKG AX132 HCDR3 (SEQ ID NO: 84) ERYGYYFDY AX132 VL amino acid sequence: (SEQ ID NO: 85) EIVLTQSPATLSLSPGERATITCRASQYVGSYLNWYQQKPGQAPRLLIYD ASNRATGIPARFSGSGSGTDFTLTISSLEPEDFAVYYCQVWDSSPPVVFG GGTKVEIK

e.g., wherein the light chain comprises the CDRs:

TABLE-US-00018 AX132 LCDR1 (SEQ ID NO: 86) RASQYVGSYLN AX132 LCDR2 (SEQ ID NO: 87) DASNRAT AX132 LCDR3 (SEQ ID NO: 88) QVWDSSPPVV AX189 VL amino acid sequence: (SEQ ID NO: 89) DIQMTQSPSSLSASVGDRVTITCRASQDVSRYLTWYQQKPGKAPKLLIYA ASSLQSGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQAYDYSLSGYVF GGGTKVEIK

e.g., wherein the light chain comprises the CDRs:

TABLE-US-00019 AX189 LCDR1 (SEQ ID NO: 90) RASQDVSRYLT AX189 LCDR2 (SEQ ID NO: 91) AASSLQS AX189 LCDR3 (SEQ ID NO: 92) QAYDYSLSGYV (SEQ ID NO: 93) AX189 VH amino acid sequence: EVQLLESGGGLVQPGGSLRLSCKASGYTFSSYWMHWVRQAPGKGLEWIGR IDPYNGGTKYNEKFKGKATISRDNSKNTLYLQMNSLRAEDTAVYYCARYG YYLGSYAMDYWGQGTLVTVSS

e.g., wherein the heavy chain comprises the CDRs:

TABLE-US-00020 AX189 HCDR1 (SEQ ID NO: 94) GYTFSSYWMH AX189 HCDR2 (SEQ ID NO: 95) RIDPYNGGTKYNEKFKG AX189 HCDR3 (SEQ ID NO: 96) YGYYLGSYAMDY 1462/1282 heavy chain amino acid sequence: (SEQ ID NO: 97) QVQLVQSGAEVKKPGASVKVSCKVS GYTFTDYYMN WVRQAPGQGLEWIG DINPNNGGAIYNQKFKG RATLTVDKSTSTAYMELRSLRSDDTAVYYCTS GIITEIAEDFWGQGTLVTVSS

e.g., wherein the heavy chain comprises the CDRs:

TABLE-US-00021 1462/1282 HCDR1 (SEQ ID NO: 98) GYTFTDYYMN, 1462/1282 HCDR2 (SEQ ID NO: 99) DINPNNGGAIYNQKFKG 1462/1282 HCDR3 (SEQ ID NO: 100) GIITEIAEDF; 1462/1282 light chain amino acid sequence: (SEQ ID NO: 101) DIQMTQSPSSLSASVGDRVTITCKASQNVGTNVVWYQQKPGKAPKALIH SASYRYSGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQYKTYPYTF GQGTKVEIKR

e.g., wherein the light chain comprises the CDRs:

TABLE-US-00022 1462/1282 LCDR1 (SEQ ID NO: 102) KASQNVGTNVV, 1462/1282 LCDR2 (SEQ ID NO: 103) SASYRYS 1462/1282 LCDR3 (SEQ ID NO: 104) QQYKTYPYT.

[0137] For example, in a embodiment of the invention, the 3M cell is used to express one or both chains of etanercept (CAS No. 185243-69-0; Drug Bank No. DB00005).

Protein Expression

[0138] The processes of the present invention include methods for expressing a polypeptide comprising steps wherein various feeds are added to an initial mammalian 3M cell growth medium. These feeds include hydrolysate feed, vitamin/salt feed, amino acid feed and nutrient feed. The present invention also includes compositions comprising a 3M cell in any of the mediums discussed herein.

[0139] The "initial mammalian cell growth medium" can be any of several types of aqueous mediums known in the art; and the meaning of this term would be readily known by any practitioner of ordinary skill in the art. Examples include EX-CELL ACF CHO medium (Sigma-Aldrich (St. Louis, Mo.)). EX-CELL ACF CHO medium is a commercial medium that is animal-component free, with HEPES, without L-glutamine. The medium contains inorganic salts, HEPES and sodium bicarbonate buffers, essential and non-essential amino acids, vitamins, recombinant human insulin, plant hydrolysates, other organic compounds, trace elements, and surfactants. The medium does not contain antibiotics, antimycotics, L-glutamine, or transferring and also contains no animal-derived proteins or other components.

[0140] Other examples of initial mammalian cell growth medium include DMEM, DMEM/F-12, F-10 Nutrient Mixture, RPMI Medium 1640, F-12 Nutrient Mixture, Medium 199, Eagle's MEM, RPMI, 293 media, and Iscove's Media. For example, Eagle's minimal essential medium (MEM) comprises L-Arginine hydrochloride (126 mg/l), L-Cystine 2HCl (31 mg/l), L-Histidine hydrochloride-H.sub.2O (42 mg/l), L-Isoleucine (52 mg/l), L-Leucine (52 mg/l), L-Lysine hydrochloride (73 mg/l), L-Methionine (15 mg/l), L-Phenylalanine (32 mg/l), L-Threonine (48 mg/l), L-Tryptophan (10 mg/l), L-Tyrosine disodium salt dehydrate (52 mg/l), L-Valine (46 mg/l), Choline chloride (1 mg/l), D-Calcium pantothenate (1 mg/l), Folic Acid (1 mg/l), Niacinamide (1 mg/l), Pyridoxal hydrochloride (1 mg/l), Riboflavin (0.1 mg/l), Thiamine hydrochloride (1 mg/l), idnositol (2 mg/l), Calcium Chloride (CaCl.sub.2) (anhyd.) (200 mg/l), Magnesium Sulfate (MgSO.sub.4) (anhyd.) (97.67 mg/l), Potassium Chloride (KCl) (400 mg/l), Sodium Bicarbonate (NaHCO.sub.3) (2200 mg/l), Sodium Chloride (NaCl) (6800 mg/l), Sodium Phosphate monobasic (NaH.sub.2PO.sub.4--H.sub.2O) (140 mg/l), D-Glucose (Dextrose) (1000 mg/l) and Phenol Red (10 mg/l).

[0141] Modified Eagle Medium (MEM) (2.times.) comprises L-Arginine hydrochloride (504 mg/l), L-Cystine (96 mg/l), L-Glutamine (870 mg/l), L-Histidine hydrochloride-H.sub.2O (168 mg/l), L-Isoleucine (208 mg/l), L-Leucine (208 mg/l), L-Lysine hydrochloride (290 mg/l), L-Methionine (60 mg/l), L-Phenylalanine (128 mg/l), L-Threonine (192 mg/l), L-Tryptophan (40 mg/l), L-Tyrosine disodium salt dehydrate (208 mg/l), L-Valine (155 mg/l), Choline chloride (4 mg/l), D-Calcium pantothenate (4 mg/l), Folic Acid (4 mg/l), Niacinamide (4 mg/l), Pyridoxal hydrochloride (4 mg/l), Riboflavin (0.4 mg/l), Thiamine hydrochloride (4 mg/l), i-Inositol (8 mg/l), Calcium Chloride (CaCl.sub.2) (anhyd.) (285 mg/l), Ferric Nitrate (Fe(NO.sub.3).sub.3''9H.sub.2O) (1 mg/l), Magnesium Sulfate (MgSO.sub.4) (anhyd.) (195 mg/l), Potassium Chloride (KCl) (800 mg/l), Sodium Bicarbonate (NaHCO.sub.3) (8400 mg/l), Sodium Chloride (NaCl) (12800 mg/l), Sodium Phosphate monobasic (NaH.sub.2PO4-H.sub.2O) (250 mg/l) and D-Glucose (Dextrose) (9000 mg/l).

[0142] RPMI Medium 1640 (1.times.) comprises Glycine (10 mg/l), L-Arginine (200 mg/l), L-Asparagine (50 mg/l), L-Aspartic acid (20 mg/l), L-Cystine 2HCl (65 mg/l), L-Glutamic Acid (20 mg/l), L-Glutamine (300 mg/l), L-Histidine (15 mg/l), L-Hydroxyproline (20 mg/l), L-Isoleucine (50 mg/l), L-Leucine (50 mg/l), L-Lysine hydrochloride (40 mg/l), L-Methionine (15 mg/l), L-Phenylalanine (15 mg/l), L-Proline (20 mg/l), L-Serine (30 mg/l), L-Threonine (20 mg/l), L-Tryptophan (5 mg/l), L-Tyrosine disodium salt dehydrate (29 mg/l), L-Valine (20), Biotin (0.2 mg/l), Choline chloride (3 mg/l), D-Calcium pantothenate (0.25 mg/l), Folic Acid (1 mg/l), Niacinamide (1 mg/l), Para-Aminobenzoic Acid (1 mg/l), Pyridoxine hydrochloride (1 mg/l), Riboflavin (0.2 mg/l), Thiamine hydrochloride (1 mg/l), Vitamin B12 (0.005 mg/l), idnositol (35 mg/l), Calcium nitrate (Ca(NO.sub.3).sub.2 4H2O) (100 mg/l), Magnesium Sulfate (MgSO.sub.4) (anhyd.) (48.84 mg/l), Potassium Chloride (KCl) (400 mg/l), Sodium Bicarbonate (NaHCO3) (2000 mg/l), Sodium Chloride (NaCl) (6000 mg/l), Sodium Phosphate dibasic (Na.sub.2HPO.sub.4) anhydrous (800 mg/l), D-Glucose (Dextrose) (2000 mg/l) and Glutathione (reduced) (1 mg/l).

[0143] Generally, for the purposes of the present invention a "hydrolysate feed" includes wheat and/or soy hydrolysates. Generally, a soy or wheat hydrolysate is the product of an enzymatic digest of soy or wheat and can be purchased commercially. Typically, the hydrolysate is in cell culture grade water and is sterile. In an embodiment of the invention, the hydrolysate is a stock solution at 200 g/liter. In an embodiment of the invention, the hydrolysate is added to the culture medium to reach a final concentration of about 10 g/liter. In an embodiment of the invention, when using either the level 3 process or the enhanced process, the hydrolysate is added to the culture medium either initially, before, with or immediately after inoculation or at about 3 days after inoculation or when viable cell density reaches over about 1.times.10.sup.6 cells/ml.

[0144] "Viable cell density" refers to the concentration of cells in the medium being analyzed (e.g., cells/ml) which are viable, e.g., capable of growth and replication (e.g., when used to inoculate a liquid culture or a solid culture medium) or capable of excluding a dye such as tryptan blue, eosin or propidium in a dye exclusion assay. Such assays are commonly known in the art.

[0145] Generally, for the purposes of the present invention, a "vitamin/salt feed" includes:

Sodium selenite e.g., at a concentration of about 7.13.times.10.sup.-4 g/liter Adenine sulfate e.g., at a concentration of about 0.0816 g/liter Adenosine e.g., at a concentration of about 0.88 g/liter Cytidine e.g., at a concentration of about 0.88 g/liter Guanosine e.g., at a concentration of about 0.88 g/liter Uridine e.g., at a concentration of about 0.88 g/liter Hypoxanthine e.g., at a concentration of about 0.59 g/liter L-citrulline e.g., at a concentration of about 0.63 g/liter L-ornithine-HCl e.g., at a concentration of about 1.28 g/liter Biotin e.g., at a concentration of about 0.014 g/liter Flavin Adenine Dinucleotide e.g., at a concentration of about 0.0025 g/liter Folic Acid e.g., at a concentration of about 0.23 g/liter Lipoic Acid e.g., at a concentration of about 0.026 g/liter Niacin e.g., at a concentration of about 1.57 g/liter Pyridoxine HCl e.g., at a concentration of about 0.15 g/liter Riboflavin e.g., at a concentration of about 0.093 g/liter Thiamine HCl e.g., at a concentration of about 0.8 g/liter Vitamin E e.g., at a concentration of about 0.0188 g/liter Vitamin B12 e.g., at a concentration of about 0.17 g/liter Choline Chloride e.g., at a concentration of about 2.51 g/liter Ethanolamine HCl e.g., at a concentration of about 0.22 g/liter idnositol e.g., at a concentration of about 3.66 g/liter Thymidine e.g., at a concentration of about 0.39 g/liter Putrescine 2HCl e.g., at a concentration of about 0.02 g/liter Progesterone e.g., at a concentration of about 0.00075 g/liter; and D-Calcium Pantothenate e.g., at a concentration of about 1.19 g/liter

[0146] In an embodiment of the invention, the vitamin/salt feed is a 50.times. stock solution. In an embodiment of the invention, the vitamin/salt feed is added to the culture medium to reach a final concentration of about 20 ml/liter. In an embodiment of the invention, the vitamin/salt feed is added to the culture between days 3 and 5, post-inoculation, or when viable cell density reaches over about 1.2.times.10.sup.6 cells/ml.

[0147] Generally, for the purposes of the present invention, an "amino acid feed" includes:

[0148] L-arginine e.g., at a concentration of about 6.32 g/liter

L-cystine e.g., at a concentration of about 1.7 g/liter L-histidine e.g., at a concentration of about 2.1 g/liter L-isoleucine e.g., at a concentration of about 2.6 g/liter L-leucine e.g., at a concentration of about 2.6 g/liter L-lysine e.g., at a concentration of about 3.6 g/liter L-Methionine e.g., at a concentration of about 0.76 g/liter L-phenylalanine e.g., at a concentration of about 1.65 g/liter L-threonine e.g., at a concentration of about 2.38 g/liter L-tryptophan e.g., at a concentration of about 0.51 g/liter L-tyrosine e.g., at a concentration of about 1.8 g/liter L-valine e.g., at a concentration of about 2.34 g/liter L-alanine e.g., at a concentration of about 0.89 g/liter L-asparagine e.g., at a concentration of about 1.5 g/liter L-aspartic acid e.g., at a concentration of about 1.33 g/liter L-glutamic acid e.g., at a concentration of about 1.47 g/liter Glycine e.g., at a concentration of about 0.75 g/liter L-proline e.g., at a concentration of about 1.15 g/liter; and L-serine e.g., at a concentration of about 1.05 g/liter

[0149] In an embodiment of the invention, two separate amino acid feed stock solutions are prepared: a 100.times. stock solution including L-alanine, L-asparagine, L-aspartic acid, L-glutamic acid, glycine, L-proline and L-serine at the concentrations set forth above; and and a 50.times. solution including L-arginine, L-cystine, L-histidine, L-isoleucine, L-leucine, L-lysine, L-Methionine, L-phenylalanine, L-threonine, L-tryptophan, L-tyrosine, and L-valine at the concentrations set forth above. These stocks can be made and added separately to the culture medium. In an embodiment of the invention, the amino acid stock solution is added to the initial medium at day 0, before, with or immediately after cell inoculation.

[0150] Generally, for the purposes of the present invention, a "nutrient feed" includes:

L-asparagine: e.g., at a concentration of about 40.6 g/liter L-proline e.g., at a concentration of about 10.81 g/liter L-isoleucine e.g., at a concentration of about 18.53 g/liter L-cysteine-HCl e.g., at a concentration of about 11.19 g/liter L-leucine e.g., at a concentration of about 16.58 g/liter L-threonine e.g., at a concentration of about 8.2 g/liter L-tyrosine e.g., at a concentration of about 9.9 g/liter L-arginine e.g., at a concentration of about 9.29 g/liter L-aspartic acid e.g., at a concentration of about 3.56 g/liter L-glutamic acid e.g., at a concentration of about 6.28 g/liter Glycine e.g., at a concentration of about 2.83 g/liter L-histidine e.g., at a concentration of about 6.23 g/liter L-methionine e.g., at a concentration of about 6.58 g/liter L-tryptophan e.g., at a concentration of about 4.93 g/liter L-lysine e.g., at a concentration of about 14.66 g/liter L-phenylalanine e.g., at a concentration of about 8.64 g/liter L-valine e.g., at a concentration of about 13.08 g/liter L-serine: e.g., at a concentration of about 13 g/liter Sodium phosphate monobasic: e.g., at a concentration of about 14.41 g/liter Zinc sulfate: e.g., at a concentration of about 0.054 g/liter Cupric sulfate: e.g., at a concentration of about 0.00016 g/liter Ammonium vanadate: e.g., at a concentration of about 0.000039 g/liter Cobalt chloride: e.g., at a concentration of about 0.000125 g/liter Nickel dichloride hexahydrate: e.g., at a concentration of about 0.00002 g/liter Sodium molybdate dehydrate: e.g., at a concentration of about 0.000008 g/liter Tin chloride dehydrate: e.g., at a concentration of about 0.000004 g/liter Manganese chloride: tetrahydrate: e.g., at a concentration of about 0.000015 g/liter

[0151] In an embodiment of the invention, the nutrient feed is a 50.times. stock solution. In an embodiment of the invention, the nutrient feed is added to the culture medium to reach a final concentration of about 20 ml/liter. In an embodiment of the invention, the nutrient feed is added to the culture between days 3 and 5, post-inoculation, or when viable cell density reaches about 1.2.times.10.sup.6 cells/ml.

[0152] Furthermore, in an embodiment of the invention, glucose (from a 2.5 M stock solution) and L-glutamine (from a 0.2 M stock solution) are added to the culture medium at any point, e.g., when the concentration of the nutrients fall below 1.5 g/liter glucose and/or 150 mg/liter L-glutamine.

[0153] The present invention also includes processes wherein the osmolality and/or the temperature of the culture is optionally shifted. The osmolality or temperature shift may be done at any point in-process.

[0154] The osmolality shift has been shown to increase culture specific productivity as well as cell viability. Typically, the initial mammalian cell growth medium has a starting osmolality of about 300 mOsm. The "osmolality shift" of the present invention, however, includes shifting the culture osmolality to from about 400 mOsM to about 500 mOsm.

[0155] Osmolality is a measure of the osmoles of solute per kilogram of solvent. Osmolality can be measured using an osmometer which measures colligative properties, such as freezing-point depression, vapor pressure, or boiling-point elevation.

[0156] Osmolality of a cell culture may be shifted by any of several means. For example, a concentrated salt solution (e.g., including 5M NaCl salts stock, 8-12 mL/L added), soy hydrolysate solution (200 g/L stock, 50-80 mL/L added), sodium carbonate or sodium bicarbonate or carbon dioxide may be added. In an embodiment of the invention, adding the nutrient feed to the medium shifts the osmolality.

[0157] In an embodiment of the invention, the temperature of the culture is optionally shifted, e.g., in a step change, from about 36.5.degree. C. (.+-.0.5.degree. C.) to between about 33.degree. C. and 35.degree. C.

[0158] Vectors, such as plasmids, including a gene to be expressed by a process of the present invention, e.g., an immunoglobulin chain such as any of those discussed herein, may be introduced into a 3M host cell by any of several methods known in the art. Transformation can be carried out, e.g., by the calcium phosphate precipitation method as described by Graham and Van der Eb, Virology, 52: 546 (1978). Other methods for introducing DNA into 3M cells such as by nuclear injection or by protoplast fusion may also be used. Methods for transformation also include electroporation, liposomal transformation and DEAE-Dextran transformation.

[0159] Host 3M cells comprising a gene to be expressed using a process of the present invention may be further selected and screened to identify the clone with the requisite characteristics for expression of a target gene. One common approach, to achieve maximal expression, involves the use of mutant cell lines and a gradual increase in the selection pressure over several months for a co-transfected selection marker such as dihydrofolate reductase (DHFR) (Kaufman et al. (1982) J. Mol. Biol. 159: 601-621; Schimke et al. (1982) Natl. Cancer Inst. Monogr. 60: 79-86). In order to achieve high production rates, a dihydrofolate reductase (DHFR) negative cell line (e.g., a CHO cell line) (Urlaub et al. (1980) Proc. Natl. Acad. Sci. USA 77: 4216-4220) is transformed with an expression vector containing a functional DHFR gene in combination with the target gene to be expressed. Amplification of the vector-inserted target genes occurs in response to addition of increasing amounts of the DHFR antagonist methotrexate (MTX) to the culture medium and clones or subpopulations carrying multiple copies of the recombinant genes are generated and can be selected (Wurm (1990) Biologicals 18:159-164). The gene amplification process typically takes several months until stable cell lines are obtained which show high target gene copy numbers and high production rates of the desired protein. 3M cells comprising a DHFR gene, as well as cells that have undergone amplification of DHFR and a target gene (e.g., an immunoglobulin gene) form part of the invention. In an embodiment of the invention, 3M cells have not undergone any amplification (e.g., DHFR amplification). In an embodiment of the invention, target genes to be expressed from the 3M cells exist in only about one copy per cell.

[0160] In an embodiment of the invention, a polynucleotide, e.g., encoding an immunoglobulin chain and/or a DHFR gene, is integrated into 3M host cell chromosomal DNA or is in a vector that is ectopic and autonomously replicating. In an embodiment of the invention, the polynucleotide of the present invention is present in the 3M cell at several copies per cell (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20). Where an expression vector has been integrated into the genomic DNA of the host 3M cell to improve stability, the copy number of the vector DNA, and, concomitantly, the amount of product which could be expressed, can be increased by selecting for cell lines in which the vector sequences have been amplified after integration into the DNA of the host cell. Integrated genes may be screened for the presence and relative amount of chromosomally incorporated DNA and corresponding mRNA and polypeptide synthesis by standard methods. For example, the presence of the desired integrate may be detected by standard procedures such as DNA sequencing, Southern blotting, Northern blotting and/or Western blotting.

[0161] A 3M cell line may also be stored in a master cell bank (MCB) and/or working cell bank (WCB). Typically, when a cell line is to be used over many manufacturing cycles, a two-tiered cell banking system consisting of a master cell bank or master seed bank (MSB) and a working cell bank can be established. A cell line is established from a single host cell clone and this cell line is used to make-up the MCB. Generally, this MCB must be characterized and extensively tested for contaminants such as bacteria, fungi, viruses and mycoplasma. A sample of cells from the MCB can be expanded to form the WCB, which is characterized for cell viability prior to use in a manufacturing process. The cells in a MCB or WCB can be stored in vials, for example, at low temperature (e.g., 0.degree. C. or lower, -20.degree. C. or -80.degree. C.).

[0162] Methods for expressing a polypeptide, e.g., an immunoglobulin, using a 3M cell of the present invention comprises, in an embodiment of the present invention:

1--expanding 3M cells expressing the polypeptide in a standard initial mammalian growth medium.

[0163] This expansion can be done, for example, in shake flasks. In an embodiment of the invention, expansion occurs by growth to about 1-2.times.10.sup.6 cells/ml, dilution of a sample of those cells (e.g., to a density of about 2.5-5.times.10.sup.5 cells/ml) and, then, regrowth to about 1-2.times.10.sup.6 cells/ml, for about 10-30 cycles.

2--inoculating an initial mammalian cell growth medium with the expanded 3M cells, to a cell density of about 2.5-5.times.10.sup.5 cells/ml, and adding supplements to the medium. The supplements are soy and/or wheat hydrolysate, amino acid feed, vitamin/salt feed, nutrient feed, glucose and L-glutamine.

[0164] The day of inoculation is "day 0", the following day is "day 1", the following day is "day 2", and so on.

[0165] Soy and/or wheat hydrolysates are added, for example, either on day 0 or after viable cell density has reached over about 10.sup.6 cells/ml. In an embodiment of the invention, the hydrolysate(s) are simply added on day 3.

[0166] Amino acid feeds (discussed herein) are added, for example, at day 0, e.g., to reach approximate final culture concentrations as set forth below (not including the concentration of any indicated component from other sources such as from the initial mammalian cell growth medium):

TABLE-US-00023 Component Final concentration in culture (mg/liter) L-arginine 126.4 L-cystine 34 L-histidine 42 L-isoleucine 52 L-leucine 52 L-lysine 72 L-Methionine 15.2 L-phenylalanine 33 L-threonine 47.6 L-tryptophan 10.2 L-tyrosine 36 L-valine 46.8 L-alanine 8.9 L-asparagine 30 L-aspartic acid 26.6 L-glutamic acid 29.4 Glycine 15 L-proline 23 L-serine 21

[0167] In an embodiment of the invention, amino acid feeds are not added to the medium.

[0168] Vitamin/salt feed solution (discussed above) is added, for example, between days 3 and 5 or when viable cell density reaches about 1.2.times.10.sup.6 cells/ml, e.g., to reach approximate final culture concentrations set forth below (not including the concentration of any indicated component from other sources such as from the initial mammalian cell growth medium):

TABLE-US-00024 Component Final culture concentrations (mg/liter) Sodium selenite 0.01426 Adenine sulfate 1.632 Adenosine 17.6 Cytidine 17.6 Guanosine 17.6 Uridine 17.6 Hypoxanthine 11.8 L-citrulline 12.6 L-ornithine-HCl 25.6 Biotin 0.28 Flavin Adenine Dinucleotide 0.05 Folic Acid 4.6 Lipoic Acid 0.52 Niacin 31.4 Pyridoxine HCl 3 Riboflavin 1.86 Thiamine HCl 16 Vitamin E 0.376 Vitamin B12 3.4 Choline Chloride 50.2 Ethanolamine HCl 4.4 i-Inositol 73.2 Thymidine 7.8 Putrescine 2HCl 0.4 Progesterone 0.015 D-Calcium Pantothenate 23.8

[0169] Some components of the vitamin/salt feed are also in other feeds such as the amino acid feed. These final culture concentrations are of the components from the vitamin/salt feed and do not reflect the cumulative concentrations of the indicated components from both the amino acid feed and the vitamin/salt feed.

[0170] Nutrient feed (discussed herein) is added, for example, between days 3 and 5 or when viable cell density reaches about 1.2.times.10.sup.6 cells/ml, e.g., to reach approximate final culture concentrations set forth below (not including the concentration of any indicated component from other sources such as from the initial mammalian cell growth medium or amino acid feed):

TABLE-US-00025 Final culture concentration Component (mg/liter) L-asparagine: 812 mg/liter L-proline 216 mg/liter L-isoleucine 370 mg/liter L-cysteine-HCl 224 mg/liter L-leucine 332 mg/liter L-threonine 164 mg/liter L-tyrosine 198 mg/liter L-arginine 186 mg/liter L-aspartic acid 71 mg/liter L-glutamic acid 126 mg/liter Glycine 57 mg/liter L-histidine 125 mg/liter L-methionine 132 mg/liter L-tryptophan 99 mg/liter L-lysine 293 mg/liter L-phenylalanine 174 mg/liter L-valine 262 mg/liter L-serine: 260 mg/liter Sodium phosphate monobasic: 288.2 mg/liter Zinc sulfate: 1.08 mg/liter Cupric sulfate: 0.0032 mg/liter Ammonium vanadate: 0.00078 mg/liter Cobalt chloride: 0.0025 mg/liter Nickel dichloride hexahydrate: 0.0004 mg/liter Sodium molybdate dehydrate: 0.00016 mg/liter Tin chloride dehydrate: 0.00008 mg/liter Manganese chloride tetrahydrate: 0.0003 mg/liter

[0171] Some components of the nutrient feed are also in other feeds such as the amino acid feed. These final culture concentrations are of the components from the nutrient feed and do not reflect the cumulative concentrations of the indicated components from both the amino acid feed and the nutrient feed.

[0172] Glucose is added, for example, when the glucose concentration in the culture medium falls below about 1.5 g/liter and L-glutamine is added, for example, when the glutamine concentration in the culture medium falls below about 150 mg/liter.

3--Optionally, harvesting the 3M cells from the production cell culture medium, e.g., when viability is below about 60%, by removing the cells from the culture medium (e.g., by lowering the temperature of the cells to about 15.degree. C., adding sodium-phosphate buffer to stabilize the pH at about 6.8 and centrifuging the culture medium to clarify it of cells). If the protein is secreted, the medium can be retained for further processing, if the protein is not secreted, the 3M cells can be retained for further processing.

[0173] Any of several methods can be used to remove the 3M cells from the medium, e.g., by centrifugation. For example, using a continuous disk-stack centrifuge, e.g., with a flow rate/sigma (cm/sec) of about 9.27.times.10.sup.-7.

[0174] Furthermore, the medium can be filtered to remove 3M cells, e.g., by depth filtration with or without a centrifuge. For example, with a centrifuge, the process can, in an embodiment of the invention, comprise use of an 8.+-.2 L broth/ft.sup.2 filter (e.g., charged cellulose filter); without a centrifuge, the process can, in an embodiment of the invention, comprise use of a 20.+-.3 L broth/ft.sup.2 filter.

[0175] In addition, the medium can be filtered through a fine filter, for example, with a 0.2 micron pore size (e.g., a PVDF filter). and;

4--Optionally further purifying the protein, e.g., antibody, for example, chromatographically.

[0176] Optionally, the osmolality of the culture is shifted to about 400 mOsm to about 500 mOsm (discussed herein). In an embodiment of the invention, this shift occurs when the cells are at a density of at or above 1.times.10.sup.6 cells/ml.

[0177] Optionally, the temperature of the 3M cell culture temperature is shifted to 33.degree. C. to about 35.degree. C. (discussed herein). In an embodiment of the invention, this shift occurs, between days 4 and 8, e.g., when the change in viable cell density over a 24 hour period is less than 10%.

[0178] In an embodiment of the invention, the 3M cell culture O.sub.2 concentration, pH and temperature conditions are continuously monitored and adjusted during cell growth. In an embodiment of the invention, O.sub.2 concentration is monitored and maintained at about 60% during cell growth; and/or pH is continuously monitored and maintained at about 6.8 (e.g., .+-.0.02) during cell growth; and/or temperature is continuously monitored and maintained at about 36.5.degree. C. (e.g., about .+-.0.5.degree. C.) during cell growth 3M cell growth can be performed in any of several systems. For example, cell growth can be done in a simple flask, e.g., a glass shake flask. Other systems include tank bioreactors, bag bioreactors and disposable bioreactors. A tank bioreactor includes, typically, a metal vessel (e.g., a stainless steel jacketed vessel) in which cells are grown in a liquid medium. Tank bioreactors can be used for a wide range of culture volumes (e.g., 100 l, 150 l, 10000 l, 15000 l). Tank bioreactors often have additional features for controlling cell growth conditions, including means for temperature control, medium agitation, controlling sparge gas concentrations, controlling pH, controlling O.sub.2 concentration, removing samples from the medium, reactor weight indication and control, cleaning hardware, sterilizing the hardware, piping or tubing to deliver all services, adding media, control pH, control solutions, and control gases, pumping sterile fluids into the growth vessel and, supervisory control and a data acquisition. Classifications of tank bioreactor include stirred tank reactors wherein mechanical stirrers (e.g., impellers) are used to mix the reactor to distribute heat and materials (such as oxygen and substrates). Bubble column reactors are tall reactors which use air alone to mix the contents. Air lift reactors are similar to bubble column reactors, but differ by the fact that they contain a draft tube. The draft tube is typically an inner tube which improves circulation and oxygen transfer and equalizes shear forces in the reactor. In fluidized bed reactors, cells are "immobilized" on small particles which move with the fluid. The small particles create a large surface area for cells to stick to and enable a high rate of transfer of oxygen and nutrients to the cells. In packed bed reactors cells are immobilized on large particles. These particles do not move with the liquid. Packed bed reactors are simple to construct and operate but can suffer from blockages and from poor oxygen transfer. A disposable bioreactor is a disposable, one-time use bioreactor. Often, disposable bioreactors possess features similar to non-disposable bioreactors (e.g., agitation system, sparge, probes, ports, etc.).

[0179] The present invention includes any liquid culture medium, comprising one or more 3M cells, generated by any of the processes set forth herein, including 3M containing culture mediums generated as intermediates during practice of any of the cell culture methods discussed herein; for example, produced by a process comprising inoculating an initial mammalian cell growth medium, pre-warmed to about 37.degree. C.; which medium comprises HEPES, sodium bicarbonate buffers, inorganic salts, non-essential amino acids, recombinant human insulin, trace elements and surfactants; and which does not comprise L-glutamine, antibiotics, antimycotics or animal-derived components; with 3M cells expressing an antibody light chain immunoglobulin and heavy chain immunoglobulin, to a cell density of about 2.5-5.times.10.sup.5 cells/ml; and, adding the following supplements to the medium before, simultaneously with or immediately after said inoculation: soy hydrolysate to a final concentration of about 10 g/liter;

and, optionally, an amino acid feed wherein the concentration of the components added by said amino acid feed are approximately those set forth below:

[0180] L-arginine: 126.4 mg/liter

[0181] L-cystine: 34 mg/liter

[0182] L-histidine: 42 mg/liter

[0183] L-isoleucine: 52 mg/liter

[0184] L-leucine: 52 mg/liter

[0185] L-lysine: 72 mg/liter

[0186] L-Methionine: 15.2 mg/liter

[0187] L-phenylalanine: 33 mg/liter

[0188] L-threonine: 47.6 mg/liter

[0189] L-tryptophan: 10.2 mg/liter

[0190] L-tyrosine: 36 mg/liter

[0191] L-valine: 46.8 mg/liter

[0192] L-alanine: 8.9 mg/liter

[0193] L-asparagine: 30 mg/liter

[0194] L-aspartic acid: 26.6 mg/liter

[0195] L-glutamic acid: 29.4 mg/liter

[0196] glycine: 15 mg/liter

[0197] L-proline: 23 mg/liter

[0198] L-serine: 21 mg/liter; and, when viable cell density reaches over about 1.2.times.10.sup.6 cells/ml, adding supplement feeds wherein the concentration of the components added by said supplement feeds are approximately those set forth below:

[0199] Sodium selenite: 0.01426 mg/liter

[0200] Adenine sulfate: 1.632 mg/liter

[0201] Adenosine: 17.6 mg/liter

[0202] Cytidine: 17.6 mg/liter

[0203] Guanosine: 17.6 mg/liter

[0204] Uridine: 17.6 mg/liter

[0205] Hypoxanthine: 11.8 mg/liter

[0206] L-citrulline: 12.6 mg/liter

[0207] L-ornithine-HCl: 25.6 mg/liter

[0208] Biotin: 0.28 mg/liter

[0209] Flavin Adenine Dinucleotide: 0.05 mg/liter

[0210] Folic Acid: 4.6 mg/liter

[0211] Lipoic Acid: 0.52 mg/liter

[0212] Niacin: 31.4 mg/liter

[0213] Pyridoxine HCl: 3 mg/liter

[0214] Riboflavin: 1.86 mg/liter

[0215] Thiamine HCl: 16 mg/liter

[0216] Vitamin E: 0.376 mg/liter

[0217] Vitamin B12: 3.4 mg/liter

[0218] Choline Chloride: 50.2 mg/liter

[0219] Ethanolamine HCl: 4.4 mg/liter

[0220] idnositol: 73.2 mg/liter

[0221] Thymidine: 7.8 mg/liter

[0222] Putrescine 2HCl: 0.4 mg/liter

[0223] Progesterone: 0.015 mg/liter

[0224] D-Calcium Pantothenate: 23.8 mg/liter

[0225] L-asparagine: 812 mg/liter

[0226] L-proline 216 mg/liter

[0227] L-isoleucine 370 mg/liter

[0228] L-cysteine-HCl 224 mg/liter

[0229] L-leucine 332 mg/liter

[0230] L-threonine 164 mg/liter

[0231] L-tyrosine 198 mg/liter

[0232] L-arginine 186 mg/liter

[0233] L-aspartic acid 71 mg/liter

[0234] L-glutamic acid 126 mg/liter

[0235] Glycine 57 mg/liter

[0236] L-histidine 125 mg/liter

[0237] L-methionine 132 mg/liter

[0238] L-tryptophan 99 mg/liter

[0239] L-lysine 293 mg/liter

[0240] L-phenylalanine 174 mg/liter

[0241] L-valine 262 mg/liter

[0242] L-serine: 260 mg/liter

[0243] Sodium phosphate monobasic: 288.2 mg/liter

[0244] Zinc sulfate: 1.08 mg/liter

[0245] Cupric sulfate: 0.0032 mg/liter

[0246] Ammonium vanadate: 0.00078 mg/liter

[0247] Cobalt chloride: 0.0025 mg/liter

[0248] Nickel dichloride hexahydrate: 0.0004 mg/liter

[0249] Sodium molybdate dehydrate: 0.00016 mg/liter; and, during cell growth, adding glucose to the medium when glucose levels fall below about 1.5 g/liter and adding L-glutamine when L-glutamine levels fall below about 150 mg/liter; and during cell growth maintaining O.sub.2 concentration at about 60%; pH at about 6.8.+-.0.02 and temperature at about 36.5.degree. C..+-.0.5.degree. C.; for example, wherein the medium comprises cells that have reached about 60% viability.

EXAMPLES

[0250] The present invention is intended to exemplify the present invention and not to be a limitation thereof. Any method or composition disclosed below falls within the scope of the present invention.

Example 1: Generation of 3M Cell Line

[0251] Previous unsuccessful attempts were made to pre-adapt CHO host cell lines for efficient growth in serum free media. One attempt was made to gradually adapt host cells into IS-CHO-V (a commercially available cell culture medium containing no animal components; available from Irvine Scientific; Santa Ana, Calif.) serum-free medium in suspension for 56 days and then re-adapt back to serum-containing medium in attachment. The cell line was named DXB-IS-A (also known as ISA).

[0252] In another attempt, a new serum-free protein-free media formulation, C5467, developed by Sigma-Aldrich Inc. was adapted to scale up antibody production for select clones. Therefore, the attempt was made to gradually adapt host cells into Sigma C5467 medium in suspension for 41 days and then re-adapt back to serum-containing medium in attachment. The cell line generated with this method was named DXB-Sig-A. This cell line was compared with ISA. The cell growth and viability, during suspension adaptation into C5467 medium, of the transfected cell lines derived from DXB-Sig-A and of the ISA cell line, were compared. However, the DXB-Sig-A cell line was found to be even harder than ISA to adapt into the C5467 medium.

[0253] Additionally, an attempt was made to simulate the newly developed strategy by abruptly adapting host cells into modified Sigma C5467 medium in suspension for 83 days. The cell line generated with this method was named DXB host (3 mo). This new cell line performed about the same as ISA. Cell growth and viability during suspension adaptation into modified C5467, of the transfected cell lines derived from the DXB host (3 mo) and of the ISA cell line, were compared.

[0254] It was concluded that a new approach, other than mere serum-free adaptation, was needed to make these cells more robust. The approach of the present invention was performed by subcloning the DXB host (3 mo) into C5467 medium in 96 well plates twice to ensure purity, recoverability, stability, and consistency in performance in serum-free environment. The new cell line that was made, 3M (also known as "DXBHost 2.times.Susp"), was found to be superior to ISA when transformed with anti-IL23, anti-HGF, or cyno-anti-TSLP expression constructs, in terms of cell growth, clone recovery, and the rate of successful clones growing and producing desirable amounts of antibody in serum-free suspension conditions.

Materials & Methods

[0255] Cell Thawing.

[0256] To revive DXB11 CHO host (3 mo) cells for expansion, a frozen vial was partially submerged into a 37.degree. C. circulating water bath until the content just thawed (about 1-2 min). The content was then transferred into a T75 flask with 20 ml host medium and then grown. A medium exchange with fresh host medium was performed the next day.

[0257] Subcloning.

[0258] When cells in the T75 flask reached about 90% confluency, cells were trypsinized and resuspended in 8 ml of host medium. Four ml of the cell suspension was centrifuged at 1000 rpm for 15 minutes. The cell pellet was resuspended with 4 ml of serum-free host medium and 100 ul of cell suspension was two-fold serial diluted across each well in the 8 rows of a 96 well plate containing 100 ul of medium in each well. Each well of the 96-well plate was supplemented with additional 100 ul of fresh serum-free host medium. The plates were incubated at 37.degree. C. in a 7.5% CO.sub.2 incubator with high humidity for 2 weeks. Cells from the wells at the dilution end point of each row were harvested and were transferred to T25 flasks containing 2 ml of serum-free host media. The T-25 flasks were maintained in a 37.degree. C. incubator with 7.5% CO.sub.2 and were agitated at 70 rpm on an orbital shaker for one week. Cells from T-25 flasks were subcloned into 96-well plates and scaled up again to T25 flasks with the procedures described above.

[0259] Cell Expansion.

[0260] Two ml of cells in T25 flask were transferred into a T75 flask with 5 ml of serum-free host media and were agitated at 70 rpm for 4 days. Cells were then transferred into shake flasks to scale up, i.e., 18 ml for 125-ml flask, 45 ml for 250-ml flask, and 135 ml for 500-ml flask, and were agitated at 105 rpm.

[0261] Cell Bank Preparation.

[0262] When the cells in the 500-ml shake flask reached a density of 1.7.times.10.sup.6 cells/ml, cells were harvested and centrifuged at 1000 rpm for 10 minutes. Cell pellets were resuspended in 20 ml of freezing medium. Cells were aliquoted into twenty 1.8 ml CryoTubes, loaded into a freezing container and placed in a -80.degree. C. freezer overnight. Frozen vials were then transferred into a liquid nitrogen freezer for long-term storage.

TABLE-US-00026 TABLE 1 List of Media (See Table 2 for the List of Components or Chemicals) Medium Name Components Growth medium (general term for Growth medium could be host the media used to grow host medium or serum-free host medium. cells or transfected cells, either in adherent or suspension mode.) Host medium MEM.alpha.+ with 10% cFBS Serum-free host medium JRH ImMEDIAte ADVANTAGE 65778 with 40 ml/L glutamine, 10 ml/L HT, 20 ml/L GSEM, 1 ml/L Trace A, 1 ml/L Trace B, 1 ml/L CD Lipid, 1 ml/L Mix 1 Freezing medium Growth medium (add 10% serum if serum-free) + 10% DMSO

TABLE-US-00027 TABLE 2 List of Materials Used Component or Chemical Name Comments MEM.alpha.+ = Minimum Essential (Gibco CAT# 12571-063) Medium with nucleotides and nucleosides cFBS* = Characterized Fetal Bovine HyClone CAT# SH30071.03 Serum, .gamma.-irradiated JRH ImMEDIAte ADVANTAGE 65778 = SAFC CAT# 65778- SAFC C5467-44 (w/o ATA (aurine 1000M3367 tricarboxylic acid), w/o L- Glutamine). Glucose 45% solution Sigma CAT# G8769 Glutamine (200 mM) Gibco CAT# 25030-081 HT = HT Supplement (100X) - mixture of Gibco CAT# 11067-030 sodium hypoxanthine and thymidine GSEM = GSEM Supplement (50X) SIGMA CAT# G9785 Mix 1 = CHO Kit 2 Iron Chelator SIGMA Trace A = Trace Elements A (1000X) Cellgro CAT# 99-182-C Trace B = Trace Elements B (1000X) Cellgro CAT# 99-175-CI CD Lipid = Chemically Defined Lipid Gibco CAT# 11905-031 Concentrate Trypsin = Trypsin-EDTA (1X) Gibco CAT# 25300-054 DMSO = Dimethyl Sulphoxide Sigma CAT# 2650

Trace Elements A (1000.times.)

[0263] 1.6 mg/l CuSO.sub.4.5H.sub.2O

[0264] 863.00 mg/l ZnSO.sub.4.7H.sub.2O

[0265] 17.30 mg/l Selenite.2Na

[0266] 1155.10 mg/l Ferric citrate

Trace Elements B (1000.times.)

[0267] 0.17 mg/l MnSO.sub.4.H2O

[0268] 140.00 mg/l Na.sub.2SiO.sub.3.9H.sub.2O

[0269] 1.24 mg/l Molybdic acid,

[0270] Ammonium salt

[0271] 0.65 mg/l NH.sub.4VO.sub.3

[0272] 0.13 mg/l NiSO.sub.4.6H.sub.2O

[0273] 0.12 mg/l SnCl (anhydrous)

Chemically Defined Lipid Concentrate

[0274] 2 mg/l Arachidonic Acid

[0275] 220 mg/l Cholesterol

[0276] 70 mg/l DL-alpha-Tocopherol Acetate

[0277] 100% Ethyl Alcohol

[0278] 10 mg/l Linoleic Acid

[0279] 10 mg/l Linolenic Acid

[0280] 10 mg/l Myristic Acid

[0281] 10 mg/l Oleic Acid

[0282] 10 mg/l Palmitic Acid

[0283] 10 mg/l Palmitoleic Acid

[0284] 90000 mg/l Pluronic F-68

[0285] 10 mg/l Stearic Acid

[0286] 2200 mg/l Tween 80.RTM.

GSEM Supplement

[0287] 450.0 mg/l L-alanine; 4261.0 mg/l L-asparagine.H.sub.2O; 650.0 mg/l L-aspartic acid; 3750.0 mg/l L-glutamic acid; 575.0 mg/l L-proline; 500.0 mg/l L-serine; 350.0 mg/l adenosine; 350.0 mg/l Guanosine; 350.0 mg/l Cytidine; 350.0 mg/l uridine; and 12.0 mg/l thymidine.

TABLE-US-00028 TABLE 3 Lab Equipment and Supplies Lab Equipments and Supplies Catalog, Part, or Model Number CEDEX Counter = CEDEX Automated Innovatis Cell Culture Analyzer 7.5% CO.sub.2 incubator Forma Scientific Model # 3950 Orbital shaker Forma Scientific Model # 416 Allegra-6R benchtop centrifuge Beckman Model # 366816 -80.degree. C. Biofreezer Forma Scientific Model # 8584 Liquid nitrogen Cryo plus 3 freezer Forma Scientific Model # 7404 Circulating water bath Precision Model # 51221035 96-well plates Falcon Cat # 353072 T-25 flasks Corning Cat # 430639 T-75 flasks Corning Cat # 430725 125 ml shake flask Corning Cat # 431143 250 ml shake flask Corning Cat # 431144 500 ml shake flask Corning Cat # 431145 1 L shake flask Corning Cat # 431147 1.8 ml CryoTube Nunc Cat # 368632 15 ml-conical tube Falcon Cat # 352097 freezing container = Controlled rate Nalgene Cat # 5100-0001 freezing container = .Mr. Frosty.

Results and Discussion

[0288] The 3M (DXBHost 2.times.Susp) cell line was compared with the old standard host cell line ISA (DXB-IS-A) in the performance of cell growth potential and antibody production. The cell growth potential was evaluated at the host cell stage (i.e., before transfection and subcloning) to avoid clonal variations. The antibody production potential of these two cell lines was evaluated at the cloning stage (i.e., after 19-days of incubation in 96-wells after transfection) and also after adaptation into suspension in serum-free media.

[0289] 3M had better cell growth potential than ISA. Both 3M and ISA cells were seeded at 0.5.times.10.sup.6 cells/ml with 60 ml serum-free host medium in 250-ml shake flasks. The flasks were agitated at 105 rpm until cell viability reached just below 40%. In batch mode (as shown in FIG. 1), 3M cells reached higher cell density (2.3.times.10.sup.6 cells/ml vs. 1.7.times.10.sup.6 cells/ml) and lasted for a longer culture time (20 days vs. 10 days) than ISA cells. This means that 3M cells were more robust than ISA cells in serum-free suspension conditions. In theory, if specific antibody productivity is the same for both cell lines after transfection, 3M would produce more antibody than ISA due to higher density and longevity of cells.

[0290] The cloning recovery efficiency of 3M and ISA cell lines was compared after transfection with vectors encoding murine anti-IL17 immunoglobulin chains. This was done by counting the number of clones, including multiple clones in single wells, recovered from five 96-well plates with the same seeding cell density. As shown in FIG. 2, the number of clones recovered from five 96 well plates were 58 for 3M and only 17 for ISA. Multiple-clone counting was performed only once. 3M had better cloning recovery efficiency than ISA in all other projects (i.e., anti-IL23 antibody, anti-hepatocyte growth factor and cyno anti-TSLP).

[0291] Both 3M and ISA cells were transfected using the vectors containing cDNAs for selection markers (i.e., dhfr & hygromycin B resistance) and for antibody light and heavy immunoglobulin chains. The antibody titers in 96 wells after subcloning for 19 days between the hosts 3M and ISA were compared for three expression constructs, anti-IL23 (3 cDNA versions), anti-HGF, and cyno-anti-TSLP.

[0292] As shown in FIG. 3, in the cases of versions 2 & 3 of anti-IL-23, the titer distribution of 3M was only slightly higher than that of ISA (at the lower range). In the cases of version 1 of anti-IL23, cyno-anti-TSLP, and first transfection of anti-HGF, the titer distribution of 3M was much higher than for that of ISA. While, for the second transfection of anti-HGF, the titer distribution was reversed, i.e., ISA was slightly higher than that of 3M. Thus, the titer distribution of 3M was statistically higher than for that of ISA. However, exceptions did exist. The reason for the exceptions may be that the comparisons were done in attachment mode (i.e., wherein cells were grown in T75 flasks in adherent culture containing serum media, instead of growing in shake-flasks in suspension condition in a serum-free medium); therefore, the advantage of the robustness (obtained by serum-free suspension adaptation and cloning) of 3M may not have been evident in this subcloning stage in 96 wells.

[0293] A key comparison between 3M and ISA is in the final stage of cell line development, i.e., in serum-free suspension mode. Since, at this stage, only a limited number of clones can be selected due to their good growth and sustainable antibody productivity, we compared the number of successful clones from 3M and ISA in different projects. Successful clones were defined, here, as cell lines with good cell growth and relatively high and stable specific productivity in serum-free suspension for over 40 generations. As described below, the majority of the successful clones from three major projects were found to be derived from 3M, instead of ISA:

[0294] For anti-IL23, there were 3 versions of cDNAs tested.

1) For version 1 anti-IL23, the only successful clone was from 3M with a specific productivity of 8 pcd (picograms per cell per day) of immunoglobulin; 2) For version 2 anti-IL23, 6 out of 7 successful clones were from 3M (FIG. 4). The specific productivity in pcd for these 3M clones were 28, 25, 22, 13 and 8. One ISA clone had a specific productivity of 12 pcd of immunoglobulin, which was low compared to that of the 3M clones. 3) For version 3 anti-IL-23, all 5 successful clone were from 3M. The specific productivity in pcd of immunoglobulin for these 3M clones were 25, 21, 19, 15 and 10.

[0295] For anti-HGF, gene non-optimized and optimized versions were generated. Factors affecting mRNA stability, e.g., GC content, ribosomal binding sites, consensus and cryptic splice sites, repeats and secondary structures, were considered during gene optimization.

1) For non-optimized versions, both of 2 successful clones were from 3M. A clone from ISA grew very well in serum-free suspension, however, the specific productivity dropped down, to become negligible, in only a few generations. 2) For optimized versions, transfected cell lines did not only produce more antibodies but also were stable for longer generations.

[0296] From the observations described above, we have concluded that 3M is a superior host as compared to ISA for cell line development in producing therapeutic antibodies, immunoglobulins and other proteins, particularly proteins of therapeutic interest.

[0297] The present invention is not to be limited in scope by the specific embodiments described herein. Indeed, the scope of the present invention includes embodiments specifically set forth herein and other embodiments not specifically set forth herein; the embodiments specifically set forth herein are not necessarily intended to be exhaustive. Various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description. Such modifications are intended to fall within the scope of the claims.

[0298] Patents, patent applications, publications, product descriptions, and protocols are cited throughout this application, the disclosures of which are incorporated herein by reference in their entireties for all purposes.

Sequence CWU 1

1

1041128PRTHomo sapiens 1Met Ser Pro Ser Gln Leu Ile Gly Phe Leu Leu Leu Trp Val Pro Ala 1 5 10 15 Ser Arg Gly Glu Ile Val Leu Thr Gln Val Pro Asp Phe Gln Ser Val 20 25 30 Thr Pro Lys Glu Lys Val Thr Ile Thr Cys Arg Ala Ser Gln Ser Ile 35 40 45 Gly Ser Ser Leu His Trp Tyr Gln Gln Lys Pro Asp Gln Ser Pro Lys 50 55 60 Leu Leu Ile Lys Tyr Ala Ser Gln Ser Leu Ser Gly Val Pro Ser Arg 65 70 75 80 Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Asn Ser 85 90 95 Leu Glu Ala Glu Asp Ala Ala Ala Tyr Tyr Cys His Gln Ser Ser Arg 100 105 110 Leu Pro His Thr Phe Gly Gly Gly Thr Lys Val Glu Ile Lys Arg Thr 115 120 125 2137PRTHomo sapiens 2Met Glu Phe Gly Leu Ser Trp Val Phe Leu Val Ala Ile Leu Lys Gly 1 5 10 15 Val Gln Cys Glu Val Gln Leu Val Gln Ser Gly Gly Gly Leu Val His 20 25 30 Pro Gly Gly Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe 35 40 45 Ser Ser Phe Ala Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu 50 55 60 Glu Trp Ile Ser Val Ile Asp Thr Arg Gly Ala Thr Tyr Tyr Ala Asp 65 70 75 80 Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser 85 90 95 Leu Tyr Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Met Ala Val Tyr 100 105 110 Tyr Cys Ala Arg Leu Gly Asn Phe Tyr Tyr Gly Met Asp Val Trp Gly 115 120 125 Gln Gly Thr Thr Val Thr Val Ser Ser 130 135 3128PRTHomo sapiens 3Met Ser Pro Ser Gln Leu Ile Gly Phe Leu Leu Leu Trp Val Pro Ala 1 5 10 15 Ser Arg Gly Glu Ile Val Leu Thr Gln Ser Pro Asp Ser Leu Ser Val 20 25 30 Thr Pro Gly Glu Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Ser Ile 35 40 45 Gly Ser Ser Leu His Trp Tyr Gln Gln Lys Pro Gly Gln Ser Pro Lys 50 55 60 Leu Leu Ile Lys Tyr Ala Ser Gln Ser Leu Ser Gly Val Pro Ser Arg 65 70 75 80 Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser 85 90 95 Leu Glu Ala Glu Asp Ala Ala Ala Tyr Tyr Cys His Gln Ser Ser Arg 100 105 110 Leu Pro His Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys Arg Thr 115 120 125 4128PRTHomo sapiens 4Met Ser Pro Ser Gln Leu Ile Gly Phe Leu Leu Leu Trp Val Pro Ala 1 5 10 15 Ser Arg Gly Glu Ile Val Leu Thr Gln Ser Pro Asp Ser Leu Ser Val 20 25 30 Thr Pro Gly Glu Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Ser Ile 35 40 45 Gly Ser Ser Leu His Trp Tyr Gln Gln Lys Pro Gly Gln Ser Pro Lys 50 55 60 Leu Leu Ile Lys Tyr Ala Ser Gln Ser Leu Ser Gly Val Pro Ser Arg 65 70 75 80 Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser 85 90 95 Leu Glu Ala Glu Asp Phe Ala Val Tyr Tyr Cys His Gln Ser Ser Arg 100 105 110 Leu Pro His Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys Arg Thr 115 120 125 5128PRTHomo sapiens 5Met Ser Pro Ser Gln Leu Ile Gly Phe Leu Leu Leu Trp Val Pro Ala 1 5 10 15 Ser Arg Gly Glu Ile Val Leu Thr Gln Ser Pro Gly Thr Leu Ser Val 20 25 30 Ser Pro Gly Glu Arg Ala Thr Leu Ser Cys Arg Ala Ser Gln Ser Ile 35 40 45 Gly Ser Ser Leu His Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Arg 50 55 60 Leu Leu Ile Lys Tyr Ala Ser Gln Ser Leu Ser Gly Ile Pro Asp Arg 65 70 75 80 Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Arg 85 90 95 Leu Glu Pro Glu Asp Ala Ala Ala Tyr Tyr Cys His Gln Ser Ser Arg 100 105 110 Leu Pro His Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys Arg Thr 115 120 125 6128PRTHomo sapiens 6Met Ser Pro Ser Gln Leu Ile Gly Phe Leu Leu Leu Trp Val Pro Ala 1 5 10 15 Ser Arg Gly Glu Ile Val Leu Thr Gln Ser Pro Gly Thr Leu Ser Val 20 25 30 Ser Pro Gly Glu Arg Ala Thr Leu Ser Cys Arg Ala Ser Gln Ser Ile 35 40 45 Gly Ser Ser Leu His Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Arg 50 55 60 Leu Leu Ile Lys Tyr Ala Ser Gln Ser Leu Ser Gly Ile Pro Asp Arg 65 70 75 80 Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Arg 85 90 95 Leu Glu Pro Glu Asp Phe Ala Val Tyr Tyr Cys His Gln Ser Ser Arg 100 105 110 Leu Pro His Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys Arg Thr 115 120 125 7137PRTHomo sapiens 7Met Glu Phe Gly Leu Ser Trp Val Phe Leu Val Ala Ile Leu Lys Gly 1 5 10 15 Val Gln Cys Glu Val Gln Leu Val Gln Ser Gly Gly Gly Leu Val Lys 20 25 30 Pro Gly Gly Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe 35 40 45 Ser Ser Phe Ala Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu 50 55 60 Glu Trp Ile Ser Val Ile Asp Thr Arg Gly Ala Thr Tyr Tyr Ala Asp 65 70 75 80 Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser 85 90 95 Leu Tyr Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr 100 105 110 Tyr Cys Ala Arg Leu Gly Asn Phe Tyr Tyr Gly Met Asp Val Trp Gly 115 120 125 Gln Gly Thr Thr Val Thr Val Ser Ser 130 135 8137PRTHomo sapiens 8Met Glu Phe Gly Leu Ser Trp Val Phe Leu Val Ala Ile Leu Lys Gly 1 5 10 15 Val Gln Cys Glu Val Gln Leu Val Gln Ser Gly Gly Gly Leu Val Gln 20 25 30 Pro Gly Gly Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe 35 40 45 Ser Ser Phe Ala Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu 50 55 60 Glu Trp Ile Ser Val Ile Asp Thr Arg Gly Ala Thr Tyr Tyr Ala Asp 65 70 75 80 Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser 85 90 95 Leu Tyr Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr 100 105 110 Tyr Cys Ala Arg Leu Gly Asn Phe Tyr Tyr Gly Met Asp Val Trp Gly 115 120 125 Gln Gly Thr Thr Val Thr Val Ser Ser 130 135 916PRTArtificial SequenceCDR 9Lys Ala Ser Lys Lys Val Thr Ile Phe Gly Ser Ile Ser Ala Leu His 1 5 10 15 107PRTArtificial SequenceCDR 10Asn Gly Ala Lys Leu Glu Ser 1 5 119PRTArtificial SequenceCDR 11Leu Gln Asn Lys Glu Val Pro Tyr Thr 1 5 125PRTArtificial SequenceCDR 12Ser Tyr Gly Ile Thr 1 5 1317PRTArtificial SequenceCDR 13Glu Asn Tyr Pro Arg Ser Gly Asn Thr Tyr Tyr Asn Glu Lys Phe Lys 1 5 10 15 Gly 1417PRTArtificial SequenceCDR 14Cys Glu Phe Ile Ser Thr Val Val Ala Pro Tyr Tyr Tyr Ala Leu Asp 1 5 10 15 Tyr 1517PRTArtificial SequenceCDR 15Ser Glu Phe Ile Ser Thr Val Val Ala Pro Tyr Tyr Tyr Ala Leu Asp 1 5 10 15 Tyr 1617PRTArtificial SequenceCDR 16Ala Glu Phe Ile Ser Thr Val Val Ala Pro Tyr Tyr Tyr Ala Leu Asp 1 5 10 15 Tyr 1717PRTArtificial SequenceCDR 17Val Glu Phe Ile Ser Thr Val Val Ala Pro Tyr Tyr Tyr Ala Leu Asp 1 5 10 15 Tyr 1817PRTArtificial SequenceCDR 18Ser Glu Phe Ile Ser Thr Val Met Ala Pro Tyr Tyr Tyr Ala Leu Asp 1 5 10 15 Tyr 1917PRTArtificial SequenceCDR 19Ser Glu Phe Thr Ser Thr Val Val Ala Pro Tyr Tyr Tyr Ala Leu Asp 1 5 10 15 Tyr 20108PRTArtificial SequenceIg light chain 20Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Arg Thr Ser Glu Asn Ile Tyr Ser Tyr 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Leu Leu Ile 35 40 45 Tyr Asn Ala Lys Thr Leu Ala Glu Gly Val Pro Ser Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro 65 70 75 80 Glu Asp Phe Ala Thr Tyr Tyr Cys Gln His His Tyr Gly Ile Pro Phe 85 90 95 Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys Arg 100 105 21116PRTArtificial SequenceIg heavy chain 21Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Ile Phe Ile Thr Tyr 20 25 30 Trp Met Thr Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Gln Ile Phe Pro Ala Ser Gly Ser Ala Asp Tyr Asn Glu Met Phe 50 55 60 Glu Gly Arg Val Thr Met Thr Thr Asp Thr Ser Thr Ser Thr Ala Tyr 65 70 75 80 Met Glu Leu Arg Ser Leu Arg Ser Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Gly Gly Gly Gly Phe Ala Tyr Trp Gly Gln Gly Thr Leu Val 100 105 110 Thr Val Ser Ser 115 22116PRTArtificial SequenceIg heavy chain 22Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Ile Phe Ile Thr Tyr 20 25 30 Trp Met Thr Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Gln Ile Phe Pro Ala Ser Gly Ser Ala Asp Tyr Ala Gln Lys Leu 50 55 60 Gln Gly Arg Val Thr Met Thr Thr Asp Thr Ser Thr Ser Thr Ala Tyr 65 70 75 80 Met Glu Leu Arg Ser Leu Arg Ser Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Gly Gly Gly Gly Phe Ala Tyr Trp Gly Gln Gly Thr Leu Val 100 105 110 Thr Val Ser Ser 115 2310PRTArtificial SequenceCDR 23Gly Phe Thr Phe Ser Ser Tyr Thr Met Ser 1 5 10 2417PRTArtificial SequenceCDR 24Thr Ile Ser Ser Gly Gly Thr Tyr Thr Tyr Tyr Pro Asp Ser Val Lys 1 5 10 15 Gly 2513PRTArtificial SequenceCDR 25Asp Asn His Ala Tyr Asp Arg Gly Pro Phe Phe Asp Tyr 1 5 10 2617PRTArtificial SequenceCDR 26Lys Ser Ser Gln Asn Leu Phe Tyr Arg Ser Asn Gln Lys Asn His Leu 1 5 10 15 Ala 277PRTArtificial SequenceCDR 27Trp Thr Ser Thr Arg Glu Ser 1 5 289PRTArtificial SequenceCDR 28Gln Gln Tyr Tyr Ser Tyr Pro Pro Thr 1 5 295PRTArtificial SequenceCDR 29Ala Tyr Gly Met Asp 1 5 3017PRTArtificial SequenceCDR 30Ser Ile Ser Pro Ser Gly Gly Arg Thr Lys Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly 3114PRTArtificial SequenceCDR 31Asp Leu Gly Gly Gly Tyr Tyr Tyr Tyr Tyr Gly Met Asp Val 1 5 10 3214PRTArtificial SequenceCDR 32Thr Gly Thr Ser Ser Asp Val Gly Gly Tyr Asn Tyr Val Ser 1 5 10 337PRTArtificial SequenceCDR 33Glu Val Ser Asn Arg Pro Ser 1 5 3412PRTArtificial SequenceCDR 34Ser Ser Tyr Thr Ser Ser Ser Thr Leu Phe Tyr Val 1 5 10 3510PRTArtificial SequenceCDR 35Gly Lys Thr Phe Trp Ser Trp Gly Ile Asn 1 5 10 3617PRTArtificial SequenceCDR 36Tyr Ile Tyr Ile Gly Thr Gly Tyr Thr Glu Pro Asn Pro Lys Tyr Lys 1 5 10 15 Gly 3710PRTArtificial SequenceCDR 37Ile Gly Gly Tyr Tyr Gly Asn Phe Ala Asp 1 5 10 3810PRTArtificial SequenceCDR 38Ile Gly Gly Tyr Tyr Gly Asn Phe Asp Gln 1 5 10 3916PRTArtificial SequenceCDR 39Arg Ser Ser Gln Ser Leu Leu Ile Ser Gly Gly Asn Thr Tyr Leu Asn 1 5 10 15 407PRTArtificial SequenceCDR 40Leu Val Ser Lys Leu Asp Gln 1 5 419PRTArtificial SequenceCDR 41Trp Gln Gly Thr Tyr Phe Pro Leu Thr 1 5 42114PRTArtificial SequenceIg light chain 42Asp Ile Val Met Thr Gln Ser Pro Leu Ser Leu Pro Val Thr Pro Gly 1 5 10 15 Glu Pro Ala Ser Ile Ser Cys Lys Ser Ser Gln Ser Leu Leu Phe Ser 20 25 30 Glu Asn Gln Lys Asn Tyr Leu Ala Trp Tyr Leu Gln Lys Pro Gly Gln 35 40 45 Ser Pro Gln Leu Leu Ile Tyr Trp Thr Ser Thr Arg Gln Ser Gly Val 50 55 60 Pro Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Lys 65 70 75 80 Ile Ser Arg Val Glu Ala Glu Asp Val Gly Val Tyr Tyr Cys Gln Gln 85 90 95 Ser Tyr Tyr Thr Pro Tyr Thr Phe Gly Gln Gly Thr Lys Val Glu Ile 100 105 110 Lys Arg 43124PRTArtificial SequenceIg heavy chain 43Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu 1 5 10 15 Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Phe Ser Leu Pro Ser His 20 25 30 Ser Val Ser Trp Ile Arg Gln Pro Pro Gly Lys Gly Leu Glu Trp Ile 35 40 45 Gly Ile Ile Trp Asn Gln Gly Gly Thr Asp Tyr Asn Ser Ala Phe Lys 50 55 60 Ser Arg Val Thr Ile Ser Val Asp Thr Ser Lys Asn Gln Phe Ser Leu 65 70 75 80 Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95 Arg Asn Ala Tyr Ile Thr Asp Tyr Tyr Tyr Glu Asn Tyr Phe Met Asp 100 105 110 Ala Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 445PRTArtificial SequenceCDR 44Thr Tyr Trp Met His 1 5 455PRTArtificial SequenceCDR 45Thr Tyr Trp Met His 1 5 4617PRTArtificial SequenceCDR 46Glu Ile Asn Pro Thr Asn Gly His Thr Asn Tyr Asn Glu Lys Phe Lys 1 5 10 15 Ser 4717PRTArtificial SequenceCDR 47Glu Ile Asn Pro Thr Asn Gly His Thr Asn Tyr Asn Pro Ser Phe Gln 1 5 10 15 Gly 4817PRTArtificial SequenceCDR 48Glu Ile Asn Pro Thr Asn Gly His Thr Asn Tyr Asn Gln Lys Phe Gln 1 5 10 15 Gly 499PRTArtificial SequenceCDR 49Asn Tyr Val Gly Ser Ile Phe Asp Tyr 1 5 509PRTArtificial SequenceCDR 50Asn Tyr Val Gly Ser Ile Phe Asp Tyr 1 5 5111PRTArtificial SequenceCDR 51Lys Ala Ser Glu Asn Val Val Ser Tyr Val Ser 1 5 10

5211PRTArtificial SequenceCDR 52Lys Ala Ser Glu Asn Val Val Ser Tyr Val Ser 1 5 10 537PRTArtificial SequenceCDR 53Gly Ala Ser Asn Arg Asn Thr 1 5 547PRTArtificial SequenceCDR 54Gly Ala Ser Asn Arg Asn Thr 1 5 557PRTArtificial SequenceCDR 55Gly Ala Ser Asn Arg Glu Ser 1 5 569PRTArtificial SequenceCDR 56Gly Gln Ser Tyr Asn Tyr Pro Tyr Thr 1 5 579PRTArtificial SequenceCDR 57Gly Gln Ser Tyr Asn Tyr Pro Tyr Thr 1 5 58119PRTArtificial SequenceIg heavy chain 58Glu Val Gln Leu Val Gln Ser Gly Gly Gly Leu Val His Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Gly Ser Gly Phe Thr Phe Arg Asn Tyr 20 25 30 Ala Met Tyr Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45 Ser Ala Ile Gly Ser Gly Gly Gly Thr Tyr Tyr Ala Asp Ser Val Lys 50 55 60 Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser Leu Tyr Leu 65 70 75 80 Gln Met Asn Ser Leu Arg Ala Glu Asp Met Ala Val Tyr Tyr Cys Ala 85 90 95 Arg Ala Pro Asn Trp Gly Ser Asp Ala Phe Asp Ile Trp Gly Gln Gly 100 105 110 Thr Met Val Thr Val Ser Ser 115 59107PRTArtificial SequenceIg light chain 59Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Gly Ile Ser Ser Trp 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Glu Lys Ala Pro Lys Ser Leu Ile 35 40 45 Tyr Ala Ala Ser Ser Leu Gln Ser Gly Val Pro Ser Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro 65 70 75 80 Glu Asp Phe Ala Thr Tyr Tyr Cys Gln Gln Tyr Asn Ser Tyr Pro Pro 85 90 95 Thr Phe Gly Pro Gly Thr Lys Val Asp Ile Lys 100 105 60118PRTArtificial SequenceIg heavy chain 60Gln Val Glu Leu Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg 1 5 10 15 Ser Gln Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser Tyr 20 25 30 Gly Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45 Ala Ile Ile Trp Phe Asp Gly Ser Ser Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Arg Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Phe Cys 85 90 95 Ala Arg Glu Leu Gly Arg Arg Tyr Phe Asp Leu Trp Gly Arg Gly Thr 100 105 110 Leu Val Ser Val Ser Ser 115 61108PRTArtificial SequenceIg light chain 61Glu Ile Val Leu Thr Gln Ser Pro Ala Thr Leu Ser Leu Ser Pro Gly 1 5 10 15 Glu Arg Ala Thr Leu Ser Cys Arg Ala Ser Gln Ser Val Ser Ser Tyr 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Arg Leu Leu Ile 35 40 45 Tyr Asp Ala Ser Lys Arg Ala Thr Gly Ile Pro Ala Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Glu Pro 65 70 75 80 Glu Asp Phe Ala Val Tyr Tyr Cys Gln Gln Arg Ser Lys Trp Pro Pro 85 90 95 Trp Thr Phe Gly Gln Gly Thr Lys Val Glu Ser Lys 100 105 62125PRTArtificial SequenceIg heavy chain 62Glu Val Gln Leu Leu Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Thr Ala Ser Gly Phe Thr Phe Ser Ser Tyr 20 25 30 Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45 Ser Ala Ile Ser Gly Ser Gly Gly Thr Thr Phe Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Arg Thr Thr Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Lys Asp Leu Gly Trp Ser Asp Ser Tyr Tyr Tyr Tyr Tyr Gly Met 100 105 110 Asp Val Trp Gly Gln Gly Thr Thr Val Thr Val Ser Ser 115 120 125 63109PRTArtificial SequenceIg light chain 63Asp Ile Gln Met Thr Gln Phe Pro Ser Ser Leu Ser Ala Ser Val Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Gly Ile Arg Asn Asp 20 25 30 Leu Gly Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile 35 40 45 Tyr Ala Ala Ser Arg Leu His Arg Gly Val Pro Ser Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro 65 70 75 80 Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gln His Asn Ser Tyr Pro Cys 85 90 95 Ser Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys Arg Thr 100 105 64130PRTArtificial SequenceIg heavy chain 64Glu Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ser 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Gly Thr Phe Ser Ser Tyr 20 25 30 Ala Ile Ser Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Gly Ile Ile Pro Ile Phe Gly Thr Ala Asn Tyr Ala Gln Lys Phe 50 55 60 Gln Gly Arg Val Thr Ile Thr Ala Asp Lys Ser Thr Ser Thr Ala Tyr 65 70 75 80 Met Glu Leu Ser Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Ala Pro Leu Arg Phe Leu Glu Trp Ser Thr Gln Asp His Tyr 100 105 110 Tyr Tyr Tyr Tyr Met Asp Val Trp Gly Lys Gly Thr Thr Val Thr Val 115 120 125 Ser Ser 130 65109PRTArtificial SequenceIg light chain 65Ser Ser Glu Leu Thr Gln Asp Pro Ala Val Ser Val Ala Leu Gly Gln 1 5 10 15 Thr Val Arg Ile Thr Cys Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala 20 25 30 Thr Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Ile Leu Val Ile Tyr 35 40 45 Gly Glu Asn Lys Arg Pro Ser Gly Ile Pro Asp Arg Phe Ser Gly Ser 50 55 60 Ser Ser Gly Asn Thr Ala Ser Leu Thr Ile Thr Gly Ala Gln Ala Glu 65 70 75 80 Asp Glu Ala Asp Tyr Tyr Cys Lys Ser Arg Asp Gly Ser Gly Gln His 85 90 95 Leu Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100 105 66119PRTArtificial SequenceIg heavy chain 66Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Gly 1 5 10 15 Thr Leu Ser Leu Thr Cys Ala Val Ser Gly Gly Ser Ile Ser Ser Ser 20 25 30 Asn Trp Trp Ser Trp Val Arg Gln Pro Pro Gly Lys Gly Leu Glu Trp 35 40 45 Ile Gly Glu Ile Tyr His Ser Gly Ser Thr Asn Tyr Asn Pro Ser Leu 50 55 60 Lys Ser Arg Val Thr Ile Ser Val Asp Lys Ser Lys Asn Gln Phe Ser 65 70 75 80 Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Trp Thr Gly Arg Thr Asp Ala Phe Asp Ile Trp Gly Gln Gly 100 105 110 Thr Trp Val Thr Val Ser Ser 115 67112PRTArtificial SequenceIg light chain 67Asp Val Val Met Thr Gln Ser Pro Leu Ser Leu Pro Val Thr Pro Gly 1 5 10 15 Glu Pro Ala Ser Ile Ser Cys Arg Ser Ser Gln Ser Leu Leu His Ser 20 25 30 Asn Gly Tyr Asn Tyr Leu Asp Trp Tyr Leu Gln Lys Pro Gly Gln Ser 35 40 45 Pro Gln Leu Leu Ile Tyr Leu Gly Ser Asn Arg Ala Ser Gly Val Pro 50 55 60 Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Lys Ile 65 70 75 80 Ser Arg Val Glu Ala Glu Asp Val Gly Val Tyr Tyr Cys Met Gln Gly 85 90 95 Thr His Trp Pro Leu Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys 100 105 110 68117PRTArtificial SequenceIg heavy chain 68Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu 1 5 10 15 Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Tyr Ser Ile Ser Gly Gly 20 25 30 Tyr Leu Trp Asn Trp Ile Arg Gln Pro Pro Gly Lys Gly Leu Glu Trp 35 40 45 Ile Gly Tyr Ile Ser Tyr Asp Gly Thr Asn Asn Tyr Lys Pro Ser Leu 50 55 60 Lys Asp Arg Val Thr Ile Ser Val Asp Thr Ser Lys Asn Gln Phe Ser 65 70 75 80 Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Tyr Gly Arg Val Phe Phe Asp Tyr Trp Gly Gln Gly Thr Leu 100 105 110 Val Thr Val Ser Ser 115 69112PRTArtificial SequenceIg light chain 69Asp Ile Val Met Thr Gln Ser Pro Leu Ser Leu Pro Val Thr Pro Gly 1 5 10 15 Glu Pro Ala Ser Ile Ser Cys Arg Ser Ser Gln Ser Ile Val His Ser 20 25 30 Asn Gly Asn Thr Tyr Leu Gln Trp Tyr Leu Gln Lys Pro Gly Gln Ser 35 40 45 Pro Gln Leu Leu Ile Tyr Lys Val Ser Asn Arg Leu Tyr Gly Val Pro 50 55 60 Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Lys Ile 65 70 75 80 Ser Arg Val Glu Ala Glu Asp Val Gly Val Tyr Tyr Cys Phe Gln Gly 85 90 95 Ser His Val Pro Trp Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys 100 105 110 70110PRTHomo sapiens 70Ser Tyr Val Leu Thr Gln Pro Pro Ser Ala Ser Gly Thr Pro Gly Gln 1 5 10 15 Arg Val Thr Ile Ser Cys Ser Gly Ser Ser Ser Asn Ile Gly Ile Asn 20 25 30 Tyr Val Tyr Trp Tyr Gln Gln Leu Pro Gly Thr Ala Pro Lys Leu Leu 35 40 45 Ile Tyr Arg Asn Asp Gln Arg Pro Ser Gly Val Pro Asp Arg Phe Ser 50 55 60 Gly Ser Lys Ser Gly Thr Ser Ala Ser Leu Ala Ile Ser Gly Leu Arg 65 70 75 80 Ser Glu Asp Glu Ala Asp Tyr Tyr Cys Ala Thr Trp Asp Asp Ser Leu 85 90 95 Ser Gly Val Val Phe Gly Gly Gly Thr Lys Val Thr Val Leu 100 105 110 71119PRTHomo sapiens 71Glu Val Gln Leu Val Gln Ser Gly Ala Glu Val Arg Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Ser Phe Thr Gly His 20 25 30 Tyr Ile His Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Trp Ile Asn Pro Tyr Ser Gly Gly Thr Asn Phe Pro Arg Glu Phe 50 55 60 Gln Gly Arg Val Thr Met Thr Arg Asp Thr Ser Val Asn Thr Val Tyr 65 70 75 80 Met Glu Leu Thr Arg Leu Thr Ser Asp Asp Thr Ser Val Tyr Tyr Cys 85 90 95 Ala Arg Asp Gln Met Val His Gly Gly Leu Asp Tyr Trp Gly Gln Gly 100 105 110 Thr Leu Val Thr Val Ser Ser 115 72119PRTHomo sapiens 72Glu Val Gln Leu Val Gln Ser Gly Ala Glu Val Arg Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Ser Phe Thr Gly His 20 25 30 Tyr Ile His Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Trp Ile Asn Pro Tyr Ser Gly Gly Thr Asn Phe Pro Arg Glu Phe 50 55 60 Gln Gly Arg Val Thr Met Thr Arg Asp Thr Ser Val Asn Thr Val Tyr 65 70 75 80 Met Glu Leu Thr Arg Leu Thr Ser Asp Asp Thr Ser Val Tyr Tyr Cys 85 90 95 Ala Arg Asp Glu Met Gln Asn Gly Gly Leu Asp Tyr Trp Gly Gln Gly 100 105 110 Thr Leu Val Thr Val Ser Ser 115 73119PRTHomo sapiens 73Glu Val Gln Leu Val Gln Ser Gly Ala Glu Val Arg Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Ser Phe Thr Gly His 20 25 30 Tyr Ile His Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Trp Ile Asn Pro Tyr Ser Gly Gly Thr Asn Phe Pro Arg Glu Phe 50 55 60 Gln Gly Arg Val Thr Met Thr Arg Asp Thr Ser Val Asn Thr Val Tyr 65 70 75 80 Met Glu Leu Thr Arg Leu Thr Ser Asp Asp Thr Ser Val Tyr Tyr Cys 85 90 95 Ala Arg Asp Glu Met Thr Arg Gly Gly Leu Asp Tyr Trp Gly Gln Gly 100 105 110 Thr Leu Val Thr Val Ser Ser 115 74119PRTHomo sapiens 74Glu Val Gln Leu Val Gln Ser Gly Ala Glu Val Arg Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Ser Phe Thr Gly His 20 25 30 Tyr Ile His Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Trp Ile Asn Pro Tyr Ser Gly Gly Thr Asn Phe Pro Arg Glu Phe 50 55 60 Gln Gly Arg Val Thr Met Thr Arg Asp Thr Ser Val Asn Thr Val Tyr 65 70 75 80 Met Glu Leu Thr Arg Leu Thr Ser Asp Asp Thr Ser Val Tyr Tyr Cys 85 90 95 Ala Arg Asp Glu Met His Val Gly Gly Leu Asp Tyr Trp Gly Gln Gly 100 105 110 Thr Leu Val Thr Val Ser Ser 115 75119PRTHomo sapiens 75Glu Val Gln Leu Val Gln Ser Gly Ala Glu Val Arg Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Ser Phe Thr Gly His 20 25 30 Tyr Ile His Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Trp Ile Asn Pro Tyr Ser Gly Gly Thr Asn Phe Pro Arg Glu Phe 50 55 60 Gln Gly Arg Val Thr Met Thr Arg Asp Thr Ser Val Asn Thr Val Tyr 65 70 75 80 Met Glu Leu Thr Arg Leu Thr Ser Asp Asp Thr Ser Val Tyr Tyr Cys 85 90 95 Ala Arg Asp Glu Met Val Trp Gly Gly Leu Asp Tyr Trp Gly Gln Gly 100 105 110 Thr Leu Val Thr Val Ser Ser 115 7699PRTHomo sapiens 76Met Lys Val Ser Ala Ala Leu Leu Cys Leu Leu Leu Ile Ala Ala Thr 1 5 10 15 Phe Ile Pro Gln Gly Leu Ala Gln Pro Asp Ala Ile Asn Ala Pro Val 20 25 30 Thr Cys Cys Tyr Asn Phe Thr Asn Arg Lys Ile Ser Val Gln Arg Leu

35 40 45 Ala Ser Tyr Arg Arg Ile Thr Ser Ser Lys Cys Pro Lys Glu Ala Val 50 55 60 Ile Phe Lys Thr Ile Val Ala Lys Glu Ile Cys Ala Asp Pro Lys Gln 65 70 75 80 Lys Trp Val Gln Asp Ser Met Asp His Leu Asp Lys Gln Thr Gln Thr 85 90 95 Pro Lys Thr 7776PRTHomo sapiens 77Gln Pro Asp Ala Ile Asn Ala Pro Val Thr Cys Cys Tyr Asn Phe Thr 1 5 10 15 Asn Arg Lys Ile Ser Val Gln Arg Leu Ala Ser Tyr Arg Arg Ile Thr 20 25 30 Ser Ser Lys Cys Pro Lys Glu Ala Val Ile Phe Lys Thr Ile Val Ala 35 40 45 Lys Glu Ile Cys Ala Asp Pro Lys Gln Lys Trp Val Gln Asp Ser Met 50 55 60 Asp His Leu Asp Lys Gln Thr Gln Thr Pro Lys Thr 65 70 75 78233PRTHomo sapiens 78Val Glu Pro Lys Ser Ser Asp Lys Thr His Thr Ser Pro Pro Ser Pro 1 5 10 15 Ala Pro Glu Leu Leu Gly Gly Pro Ser Val Phe Leu Phe Pro Pro Lys 20 25 30 Pro Lys Asp Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr Cys Val 35 40 45 Val Val Asp Val Ser His Glu Asp Pro Glu Val Lys Phe Asn Trp Tyr 50 55 60 Val Asp Gly Val Glu Val His Asn Ala Lys Thr Lys Pro Arg Glu Glu 65 70 75 80 Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser Val Leu Thr Val Leu His 85 90 95 Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser Asn Lys 100 105 110 Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile Ser Lys Ala Lys Gly Gln 115 120 125 Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro Pro Ser Arg Asp Glu Leu 130 135 140 Thr Lys Asn Gln Val Ser Leu Thr Cys Leu Val Lys Gly Phe Tyr Pro 145 150 155 160 Ser Asp Ile Ala Val Glu Trp Glu Ser Asn Gly Gln Pro Glu Asn Asn 165 170 175 Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser Asp Gly Ser Phe Phe Leu 180 185 190 Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg Trp Gln Gln Gly Asn Val 195 200 205 Phe Ser Cys Ser Val Met His Glu Ala Leu His Asn His Tyr Thr Gln 210 215 220 Lys Ser Leu Ser Leu Ser Pro Gly Lys 225 230 79219PRTArtificial Sequencehumanized immunoglobulin 79Asp Ile Val Met Thr Gln Ser Pro Leu Ser Leu Pro Val Thr Pro Gly 1 5 10 15 Glu Pro Ala Ser Ile Ser Cys Arg Ser Ser Gln Ser Ile Val His Ser 20 25 30 Asn Gly Asn Thr Tyr Leu Gln Trp Tyr Leu Gln Lys Pro Gly Gln Ser 35 40 45 Pro Gln Leu Leu Ile Tyr Lys Val Ser Asn Arg Leu Tyr Gly Val Pro 50 55 60 Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Lys Ile 65 70 75 80 Ser Arg Val Glu Ala Glu Asp Val Gly Val Tyr Tyr Cys Phe Gln Gly 85 90 95 Ser His Val Pro Trp Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys 100 105 110 Arg Thr Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu 115 120 125 Gln Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe 130 135 140 Tyr Pro Arg Glu Ala Lys Val Gln Trp Lys Val Asp Asn Ala Leu Gln 145 150 155 160 Ser Gly Asn Ser Gln Glu Ser Val Thr Glu Gln Asp Ser Lys Asp Ser 165 170 175 Thr Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu 180 185 190 Lys His Lys Val Tyr Ala Cys Glu Val Thr His Gln Gly Leu Ser Ser 195 200 205 Pro Val Thr Lys Ser Phe Asn Arg Gly Glu Cys 210 215 80447PRTArtificial Sequencehumanized immunoglobulin 80Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu 1 5 10 15 Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Tyr Ser Ile Thr Gly Gly 20 25 30 Tyr Leu Trp Asn Trp Ile Arg Gln Pro Pro Gly Lys Gly Leu Glu Trp 35 40 45 Ile Gly Tyr Ile Ser Tyr Asp Gly Thr Asn Asn Tyr Lys Pro Ser Leu 50 55 60 Lys Asp Arg Val Thr Ile Ser Arg Asp Thr Ser Lys Asn Gln Phe Ser 65 70 75 80 Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Tyr Gly Arg Val Phe Phe Asp Tyr Trp Gly Gln Gly Thr Leu 100 105 110 Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu 115 120 125 Ala Pro Ser Ser Lys Ser Thr Ser Gly Gly Thr Ala Ala Leu Gly Cys 130 135 140 Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser 145 150 155 160 Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu Gln Ser 165 170 175 Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser Ser Ser 180 185 190 Leu Gly Thr Gln Thr Tyr Ile Cys Asn Val Asn His Lys Pro Ser Asn 195 200 205 Thr Lys Val Asp Lys Arg Val Glu Pro Lys Ser Cys Asp Lys Thr His 210 215 220 Thr Cys Pro Pro Cys Pro Ala Pro Glu Leu Leu Gly Gly Pro Ser Val 225 230 235 240 Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr 245 250 255 Pro Glu Val Thr Cys Val Val Val Asp Val Ser His Glu Asp Pro Glu 260 265 270 Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys 275 280 285 Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser 290 295 300 Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys 305 310 315 320 Cys Lys Val Ser Asn Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile 325 330 335 Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro 340 345 350 Pro Ser Arg Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu 355 360 365 Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn 370 375 380 Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser 385 390 395 400 Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg 405 410 415 Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu 420 425 430 His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Pro Gly Lys 435 440 445 81118PRTArtificial Sequenceimmunoglobulin 81Glu Val Gln Leu Leu Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Lys Ala Ser Gly Tyr Thr Phe Ser Ser Tyr 20 25 30 Gly Met Tyr Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Ile 35 40 45 Gly Trp Ile Asp Pro Gly Ser Gly Gly Thr Lys Tyr Asn Glu Lys Phe 50 55 60 Lys Gly Lys Ala Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Glu Arg Tyr Gly Tyr Tyr Phe Asp Tyr Trp Gly Gln Gly Thr 100 105 110 Leu Val Thr Val Ser Ser 115 8210PRTArtificial Sequenceimmunoglobulin 82Gly Tyr Thr Phe Ser Ser Tyr Gly Met Tyr 1 5 10 8317PRTArtificial Sequenceimmunoglobulin 83Trp Ile Asp Pro Gly Ser Gly Gly Thr Lys Tyr Asn Glu Lys Phe Lys 1 5 10 15 Gly 849PRTArtificial Sequenceimmunoglobulin 84Glu Arg Tyr Gly Tyr Tyr Phe Asp Tyr 1 5 85108PRTArtificial Sequenceimmunoglobulin 85Glu Ile Val Leu Thr Gln Ser Pro Ala Thr Leu Ser Leu Ser Pro Gly 1 5 10 15 Glu Arg Ala Thr Ile Thr Cys Arg Ala Ser Gln Tyr Val Gly Ser Tyr 20 25 30 Leu Asn Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Arg Leu Leu Ile 35 40 45 Tyr Asp Ala Ser Asn Arg Ala Thr Gly Ile Pro Ala Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Glu Pro 65 70 75 80 Glu Asp Phe Ala Val Tyr Tyr Cys Gln Val Trp Asp Ser Ser Pro Pro 85 90 95 Val Val Phe Gly Gly Gly Thr Lys Val Glu Ile Lys 100 105 8611PRTArtificial Sequenceimmunoglobulin 86Arg Ala Ser Gln Tyr Val Gly Ser Tyr Leu Asn 1 5 10 877PRTArtificial Sequenceimmunoglobulin 87Asp Ala Ser Asn Arg Ala Thr 1 5 8810PRTArtificial Sequenceimmunoglobulin 88Gln Val Trp Asp Ser Ser Pro Pro Val Val 1 5 10 89109PRTArtificial Sequenceimmunoglobulin 89Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Asp Val Ser Arg Tyr 20 25 30 Leu Thr Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Leu Leu Ile 35 40 45 Tyr Ala Ala Ser Ser Leu Gln Ser Gly Val Pro Ser Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro 65 70 75 80 Glu Asp Phe Ala Thr Tyr Tyr Cys Gln Ala Tyr Asp Tyr Ser Leu Ser 85 90 95 Gly Tyr Val Phe Gly Gly Gly Thr Lys Val Glu Ile Lys 100 105 9011PRTArtificial Sequenceimmunoglobulin 90Arg Ala Ser Gln Asp Val Ser Arg Tyr Leu Thr 1 5 10 917PRTArtificial Sequenceimmunoglobulin 91Ala Ala Ser Ser Leu Gln Ser 1 5 9211PRTArtificial Sequenceimmunoglobulin 92Gln Ala Tyr Asp Tyr Ser Leu Ser Gly Tyr Val 1 5 10 93121PRTArtificial Sequenceimmunoglobulin 93Glu Val Gln Leu Leu Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Lys Ala Ser Gly Tyr Thr Phe Ser Ser Tyr 20 25 30 Trp Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Ile 35 40 45 Gly Arg Ile Asp Pro Tyr Asn Gly Gly Thr Lys Tyr Asn Glu Lys Phe 50 55 60 Lys Gly Lys Ala Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Tyr Gly Tyr Tyr Leu Gly Ser Tyr Ala Met Asp Tyr Trp Gly 100 105 110 Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 9410PRTArtificial Sequenceimmunoglobulin 94Gly Tyr Thr Phe Ser Ser Tyr Trp Met His 1 5 10 9517PRTArtificial Sequenceimmunoblobulin 95Arg Ile Asp Pro Tyr Asn Gly Gly Thr Lys Tyr Asn Glu Lys Phe Lys 1 5 10 15 Gly 9612PRTArtificial Sequenceimmunoglobulin 96Tyr Gly Tyr Tyr Leu Gly Ser Tyr Ala Met Asp Tyr 1 5 10 97119PRTArtificial Sequenceimmunoglobulin 97Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Val Ser Gly Tyr Thr Phe Thr Asp Tyr 20 25 30 Tyr Met Asn Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Ile 35 40 45 Gly Asp Ile Asn Pro Asn Asn Gly Gly Ala Ile Tyr Asn Gln Lys Phe 50 55 60 Lys Gly Arg Ala Thr Leu Thr Val Asp Lys Ser Thr Ser Thr Ala Tyr 65 70 75 80 Met Glu Leu Arg Ser Leu Arg Ser Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Thr Ser Gly Ile Ile Thr Glu Ile Ala Glu Asp Phe Trp Gly Gln Gly 100 105 110 Thr Leu Val Thr Val Ser Ser 115 9810PRTArtificial Sequenceimmunoglobulin 98Gly Tyr Thr Phe Thr Asp Tyr Tyr Met Asn 1 5 10 9917PRTArtificial Sequenceimmunoglobulin 99Asp Ile Asn Pro Asn Asn Gly Gly Ala Ile Tyr Asn Gln Lys Phe Lys 1 5 10 15 Gly 10010PRTArtificial Sequenceimmunoglobulin 100Gly Ile Ile Thr Glu Ile Ala Glu Asp Phe 1 5 10 101108PRTArtificial Sequenceimmunoglobulin 101Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Lys Ala Ser Gln Asn Val Gly Thr Ala 20 25 30 Val Val Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Ala Leu Ile 35 40 45 His Ser Ala Ser Tyr Arg Tyr Ser Gly Val Pro Ser Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro 65 70 75 80 Glu Asp Phe Ala Thr Tyr Tyr Cys Gln Gln Tyr Lys Gln Tyr Pro Tyr 85 90 95 Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys Arg 100 105 10211PRTArtificial Sequenceimmunoglobulin 102Lys Ala Ser Gln Asn Val Gly Thr Ala Val Val 1 5 10 1037PRTArtificial Sequenceimmunoglobulin 103Ser Ala Ser Tyr Arg Tyr Ser 1 5 1049PRTArtificial Sequenceimmunoglobulin 104Gln Gln Tyr Lys Gln Tyr Pro Tyr Thr 1 5

Claims

1. An isolated Chinese hamster ovary cell deposited at the American Type Culture Collection under deposit number PTA-10481 that comprises an immunoglobulin light chain or an immunoglobulin heavy chain or both.

2. The cell of claim 1 that comprises both an immunoglobulin light chain and an immunoglobulin heavy chain.

3. The cell of claim 1 in an aqueous liquid cell culture medium.

4. The cell of claim 1 in a vessel.

5. A master cell bank or working cell bank comprising the cell of claim 1.

6. The cell of claim 1 in a cell freezing medium.

7. The cell of claim 7 wherein the cell freezing medium comprises dimethylsulfoxide.

8. The cell of claim 1 which comprises the immunoglobulin light chain or the immunoglobulin heavy chain of an anti-IL23 antibody, an anti-PD1 antibody, an anti-TSLP antibody, an anti-HGF antibody, an anti-IL17 antibody, an anti-IL23 receptor antibody or an anti-BTLA antibody.

9. The cell of claim 10 which comprises the immunoglobulin light chain or the immunoglobulin heavy chain of an anti-PD1 antibody.

10. The cell of claim 11 which comprises the immunoglobulin light chain and the immunoglobulin heavy chain of an anti-PD1 antibody.

11. A method for making an immunoglobulin heavy chain or an immunoglobulin light chain of an anti-PD1 antibody or antigen-binding fragment thereof; comprising introducing one or more polynucleotides encoding said chain into an isolated Chinese hamster ovary cell deposited at the American Type Culture Collection under deposit number PTA-10481 and culturing the cell comprising the polynucleotides in conditions under which the chain is produced.

12. The method of claim 11 for making an immunoglobulin heavy chain and an immunoglobulin light chain of an anti-PD1 antibody comprising introducing one or more polynucleotides encoding said chains into an isolated Chinese hamster ovary cell deposited at the American Type Culture Collection under deposit number PTA-10481 and culturing the cell comprising the polynucleotides in conditions under which the chains are produced.

13. The method of claim 12 further comprising isolating the chain.

14. The method of claim 12 wherein the immunoglobulin light chain is linked to a kappa constant immunoglobulin chain and the immunoglobulin heavy chain is linked to a gamma-4 constant immunoglobulin chain.

15. A method for producing an anti-PD1 antibody comprising inoculating an initial mammalian cell growth medium, pre-warmed to about 37.degree. C.; which initial medium comprises HEPES, sodium bicarbonate buffers, inorganic salts, non-essential amino acids, recombinant human insulin, trace elements and surfactants; and which does not comprise L-glutamine, antibiotics, antimycotics or animal-derived components; with one or more cells of claim 1 expressing the antibody light chain immunoglobulin and heavy chain immunoglobulin, to a cell density of about 2.5-5.times.10.sup.5 cells/ml; and, adding the following supplements to the medium before, simultaneously with or immediately after said inoculation: soy hydrolysate to a final concentration of about 10 g/liter; and, optionally, an amino acid feed wherein the concentration of the components added by said amino acid feed are approximately those set forth below: L-arginine: 126.4 mg/liter L-cystine: 34 mg/liter L-histidine: 42 mg/liter L-isoleucine: 52 mg/liter L-leucine: 52 mg/liter L-lysine: 72 mg/liter L-Methionine: 15.2 mg/liter L-phenylalanine: 33 mg/liter L-threonine: 47.6 mg/liter L-tryptophan: 10.2 mg/liter L-tyrosine: 36 mg/liter L-valine: 46.8 mg/liter L-alanine: 8.9 mg/liter L-asparagine: 30 mg/liter L-aspartic acid: 26.6 mg/liter L-glutamic acid: 29.4 mg/liter glycine: 15 mg/liter L-proline: 23 mg/liter L-serine: 21 mg/liter; and, when viable cell density reaches over about 1.2.times.10.sup.6 cells/ml, adding supplement feeds wherein the concentration of the components added by said supplement feeds are approximately those set forth below: Sodium selenite: 0.01426 mg/liter Adenine sulfate: 1.632 mg/liter Adenosine: 17.6 mg/liter Cytidine: 17.6 mg/liter Guanosine: 17.6 mg/liter Uridine: 17.6 mg/liter Hypoxanthine: 11.8 mg/liter L-citrulline: 12.6 mg/liter L-ornithine-HCl: 25.6 mg/liter Biotin: 0.28 mg/liter Flavin Adenine Dinucleotide: 0.05 mg/liter Folic Acid: 4.6 mg/liter Lipoic Acid: 0.52 mg/liter Niacin: 31.4 mg/liter Pyridoxine HCl: 3 mg/liter Riboflavin: 1.86 mg/liter Thiamine HCl: 16 mg/liter Vitamin E: 0.376 mg/liter Vitamin B12: 3.4 mg/liter Choline Chloride: 50.2 mg/liter Ethanolamine HCl: 4.4 mg/liter i-Inositol: 73.2 mg/liter Thymidine: 7.8 mg/liter Putrescine 2HCl: 0.4 mg/liter Progesterone: 0.015 mg/liter D-Calcium Pantothenate: 23.8 mg/liter L-asparagine: 812 mg/liter L-proline 216 mg/liter L-isoleucine 370 mg/liter L-cysteine-HCl 224 mg/liter L-leucine 332 mg/liter L-threonine 164 mg/liter L-tyrosine 198 mg/liter L-arginine 186 mg/liter L-aspartic acid 71 mg/liter L-glutamic acid 126 mg/liter Glycine 57 mg/liter L-histidine 125 mg/liter L-methionine 132 mg/liter L-tryptophan 99 mg/liter L-lysine 293 mg/liter L-phenylalanine 174 mg/liter L-valine 262 mg/liter L-serine: 260 mg/liter Sodium phosphate monobasic: 288.2 mg/liter Zinc sulfate: 1.08 mg/liter Cupric sulfate: 0.0032 mg/liter Ammonium vanadate: 0.00078 mg/liter Cobalt chloride: 0.0025 mg/liter Nickel dichloride hexahydrate: 0.0004 mg/liter Sodium molybdate dehydrate: 0.00016 mg/liter; and, maintaining glucose concentration in the medium at about 1.5 g/liter and maintaining L-glutamine concentration in the medium at about 150 mg/liter; and during cell growth maintaining O.sub.2 concentration at about 60%; pH at about 6.8+0.02 and temperature at about 36.5.degree. C.+0.5.degree. C.; and, optionally, removing the host cells from the medium when cell viability is below about 60%.

16. The method of claim 15 further comprising recovering the culture medium from the cells by disk-stack centrifuging the medium, depth filtering the medium and filtering the medium through a filter with about a 0.2 micron pore size.

17. The method of claim 16 further comprising purifying the immunoglobulins from the medium by column chromatographic fractionation.