WO2011163311A1 - Mice expressing alight chain with human lambda variable and mouse constant regions - Google Patents

Mice expressing alight chain with human lambda variable and mouse constant regions Download PDF

Info

Publication number
WO2011163311A1
WO2011163311A1 PCT/US2011/041366 US2011041366W WO2011163311A1 WO 2011163311 A1 WO2011163311 A1 WO 2011163311A1 US 2011041366 W US2011041366 W US 2011041366W WO 2011163311 A1 WO2011163311 A1 WO 2011163311A1
Authority
WO
WIPO (PCT)
Prior art keywords
mouse
human
light chain
gene
locus
Prior art date
Application number
PCT/US2011/041366
Other languages
French (fr)
Inventor
Lynn Macdonald
Sean Stevens
Cagan Gurer
Andrew J. Murphy
Karolina A. Hosiawa
Original Assignee
Regeneron Pharmaceuticals, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to MX2015009162A priority Critical patent/MX347322B/en
Priority to SI201130867A priority patent/SI2480675T1/en
Priority to JP2013516714A priority patent/JP5988969B2/en
Priority to CA2804311A priority patent/CA2804311C/en
Priority to IL300712A priority patent/IL300712B1/en
Priority to MEP-2016-132A priority patent/ME02440B/en
Priority to CN201180038415.2A priority patent/CN103068994B/en
Priority to KR1020197037332A priority patent/KR102211911B1/en
Priority to ES11728508.0T priority patent/ES2575223T3/en
Priority to SG2012093258A priority patent/SG186390A1/en
Priority to BR112012033248A priority patent/BR112012033248A2/en
Priority to LTEP11728508.0T priority patent/LT2480675T/en
Priority to KR1020137001586A priority patent/KR101945352B1/en
Priority to RS20160483A priority patent/RS54891B1/en
Priority to IL313063A priority patent/IL313063A/en
Priority to KR1020197002870A priority patent/KR101991234B1/en
Priority to AU2011271043A priority patent/AU2011271043B8/en
Priority to DK11728508.0T priority patent/DK2480675T3/en
Priority to EP11728508.0A priority patent/EP2480675B1/en
Priority to KR1020217017823A priority patent/KR102462042B1/en
Application filed by Regeneron Pharmaceuticals, Inc. filed Critical Regeneron Pharmaceuticals, Inc.
Priority to KR1020227037565A priority patent/KR20220150430A/en
Priority to NZ605751A priority patent/NZ605751A/en
Priority to MX2012015300A priority patent/MX336344B/en
Priority to KR1020197017074A priority patent/KR102059909B1/en
Priority to KR1020217002982A priority patent/KR102266097B1/en
Priority to RU2013102596/10A priority patent/RU2590594C2/en
Priority to KR1020197002903A priority patent/KR102001430B1/en
Publication of WO2011163311A1 publication Critical patent/WO2011163311A1/en
Priority to HK12111457.9A priority patent/HK1170766A1/en
Priority to IL223719A priority patent/IL223719A/en
Priority to ZA2013/00063A priority patent/ZA201300063B/en
Priority to AU2015275243A priority patent/AU2015275243B2/en
Priority to IL244450A priority patent/IL244450A/en
Priority to CY20161100585T priority patent/CY1117692T1/en
Priority to SM201600213T priority patent/SMT201600213B/en
Priority to HRP20160794TT priority patent/HRP20160794T1/en
Priority to IL255179A priority patent/IL255179B/en
Priority to IL259965A priority patent/IL259965B/en
Priority to IL264634A priority patent/IL264634B/en
Priority to IL269078A priority patent/IL269078B/en
Priority to IL282872A priority patent/IL282872B/en
Priority to IL291301A priority patent/IL291301B2/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
    • C12N5/06—Animal cells or tissues; Human cells or tissues
    • C12N5/0602—Vertebrate cells
    • C12N5/0603—Embryonic cells ; Embryoid bodies
    • C12N5/0606—Pluripotent embryonic cells, e.g. embryonic stem cells [ES]
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K67/00—Rearing or breeding animals, not otherwise provided for; New or modified breeds of animals
    • A01K67/027—New or modified breeds of vertebrates
    • A01K67/0275—Genetically modified vertebrates, e.g. transgenic
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K67/00—Rearing or breeding animals, not otherwise provided for; New or modified breeds of animals
    • A01K67/027—New or modified breeds of vertebrates
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K67/00—Rearing or breeding animals, not otherwise provided for; New or modified breeds of animals
    • A01K67/027—New or modified breeds of vertebrates
    • A01K67/0275—Genetically modified vertebrates, e.g. transgenic
    • A01K67/0278—Knock-in vertebrates, e.g. humanised vertebrates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/46—Hybrid immunoglobulins
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/46—Hybrid immunoglobulins
    • C07K16/461—Igs containing Ig-regions, -domains or -residues form different species
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/46—Hybrid immunoglobulins
    • C07K16/461—Igs containing Ig-regions, -domains or -residues form different species
    • C07K16/462—Igs containing a variable region (Fv) from one specie and a constant region (Fc) from another
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
    • C12N15/8509—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells for producing genetically modified animals, e.g. transgenic
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K2207/00—Modified animals
    • A01K2207/15—Humanized animals
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K2217/00—Genetically modified animals
    • A01K2217/05—Animals comprising random inserted nucleic acids (transgenic)
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K2217/00—Genetically modified animals
    • A01K2217/05—Animals comprising random inserted nucleic acids (transgenic)
    • A01K2217/052—Animals comprising random inserted nucleic acids (transgenic) inducing gain of function
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K2217/00—Genetically modified animals
    • A01K2217/07—Animals genetically altered by homologous recombination
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K2217/00—Genetically modified animals
    • A01K2217/07—Animals genetically altered by homologous recombination
    • A01K2217/072—Animals genetically altered by homologous recombination maintaining or altering function, i.e. knock in
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K2217/00—Genetically modified animals
    • A01K2217/15—Animals comprising multiple alterations of the genome, by transgenesis or homologous recombination, e.g. obtained by cross-breeding
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K2227/00—Animals characterised by species
    • A01K2227/10—Mammal
    • A01K2227/105—Murine
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K2267/00—Animals characterised by purpose
    • A01K2267/01—Animal expressing industrially exogenous proteins
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K2267/00—Animals characterised by purpose
    • A01K2267/02—Animal zootechnically ameliorated
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K2267/00—Animals characterised by purpose
    • A01K2267/03—Animal model, e.g. for test or diseases
    • A01K2267/035—Animal model for multifactorial diseases
    • A01K2267/0381—Animal model for diseases of the hematopoietic system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/10—Immunoglobulins specific features characterized by their source of isolation or production
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/10—Immunoglobulins specific features characterized by their source of isolation or production
    • C07K2317/14—Specific host cells or culture conditions, e.g. components, pH or temperature
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/515—Complete light chain, i.e. VL + CL
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C07K2317/64—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising a combination of variable region and constant region components
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
    • C12N15/8509—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells for producing genetically modified animals, e.g. transgenic
    • C12N2015/8518—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells for producing genetically modified animals, e.g. transgenic expressing industrially exogenous proteins, e.g. for pharmaceutical use, human insulin, blood factors, immunoglobulins, pseudoparticles
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2800/00—Nucleic acids vectors
    • C12N2800/30—Vector systems comprising sequences for excision in presence of a recombinase, e.g. loxP or FRT

Definitions

  • mice that comprise a mouse or human lambda variable ( ⁇ ⁇ ) light chain sequence operably linked with a mouse or human light chain constant region ( ⁇ or kappa(i)).
  • Genetically modified mice that express epitope-binding proteins that comprise an immunoglobulin light chain comprising a variable domain derived from a human lambda variable (hX ⁇ ) gene segment, a human lambda J (hJ ) gene segment, and a mouse light chain constant (C L ) domain.
  • Genetically modified mice comprising an unrearranged immunoglobulin lambda ( ⁇ ) light chain variable nucleic acid sequence at an endogenous mouse light chain locus.
  • Mice capable of rearranging and expressing a chimeric human ⁇ /mouse CL light chain from an endogenous light chain locus that comprises a replacement of all endogenous mouse light chain variable region gene segments with one or more hV gene segments and one or more ⁇ gene segments.
  • Somatically mutated antibodies comprising hN/ ⁇ domains and mouse CL domains.
  • mice that express antibodies that are fully human, or partly human and partly mouse are known in the art.
  • transgenic mice that express fully human antibodies from transgenes containing human light and heavy chain immunoglobulin variable region genes have been reported.
  • Genetically modified mice that comprise a replacement of the endogenous mouse heavy chain variable region (HCVR) gene segments and kappa ( ⁇ ) light chain variable region (LCVR) gene segments with human HCVR and LCVR gene segments and that make chimeric antibodies with a chimeric human/mouse kappa chain are known as well.
  • Antibody light chains are encoded by one of two separate loci: kappa ( ⁇ ) and lambda ( ⁇ ).
  • Mouse antibody light chains are primarily of the ⁇ type. The ratio of ⁇ to ⁇ light chain usage in humans is about 60:40, whereas in mice it is about 95:5. Biased usage of ⁇ light chains in mice is reportedly sustained in genetically modified mice capable of expressing fully or partly human antibodies. Thus, mice that express fully or partly human antibodies appear to be constrained in lambda variable usage.
  • mice that express fully or partly human antibodies wherein the mice display an increased lambda variable ( ⁇ ) usage.
  • mice that express fully or partly human antibodies wherein the mice display an increased ⁇ variable ( ⁇ / ⁇ ) usage.
  • mice, embryos, cells, tissues, as well as nucleic acid constructs for modifying mice, and methods and compositions for making and using them are provided.
  • Mice and cells that generate lambda ( ⁇ ) variable regions (human or non- human) in the context of a kappa ( ⁇ ) light chain are provided.
  • Mice and cells that generate human ⁇ variable regions in the context of a ⁇ or a ⁇ light chain, e.g. , from an endogenous mouse light chain locus are also provided.
  • methods for making antibodies that comprise lambda variable regions are also provided. Methods for selecting heavy chains that express with cognate lambda variable regions are also provided.
  • Chimeric and human antigen-binding proteins e.g., antibodies
  • nucleic acids encoding them are provided that comprise somatically mutated variable regions, including antibodies that have light chains comprising a variable domain derived from a human ⁇ and a human ⁇ gene segment fused to a mouse light chain constant domain.
  • a mouse that expresses a human ⁇ variable region sequence on a light chain that comprises a mouse constant region.
  • a mouse is provided that expresses a human ⁇ variable region sequence on a light chain that comprises a ⁇ constant region.
  • a mouse is provided that expresses from an endogenous mouse light chain locus a light chain that comprises a human ⁇ variable region sequence.
  • a mouse is provided that comprises a rearranged light chain gene that comprises a human ⁇ variable sequence linked to a mouse constant region sequence; in one embodiment, the mouse constant region sequence is a ⁇ constant sequence; in one embodiment, the mouse constant region sequence is a ⁇ constant sequence.
  • a genetically modified mouse comprising an unrearranged human ⁇ light chain variable gene segment (hN ⁇ ) and a human ⁇ joining gene segment (hJX).
  • the unrearranged hVX and hJ are at a mouse light chain locus.
  • the unrearranged hN ⁇ and unrearranged hJ are on a transgene and operably linked to a human or mouse constant region sequence.
  • the unrearranged hV and unrearranged ⁇ are on an episome.
  • the mouse is capable of making an immunoglobulin that comprises a light chain that is derived from an unrearranged hN ⁇ sequence and a ⁇ sequence and a mouse light chain constant region (C L ) nucleic acid sequence.
  • Methods and compositions for making and using genetically modified mice are also provided.
  • Antibodies are provided that comprise (a) a human heavy chain variable domain (hV H ) fused to a mouse heavy chain constant region, and (b) a human ⁇ fused to a mouse CL domain; including wherein one or more of the variable domains are somatically mutated, e.g. , during antibody or immune cell selection in a mouse of the invention.
  • the unrearranged hX ⁇ and unrearranged hJ are operably linked with a human or mouse ⁇ constant region (CK). In one embodiment, the unrearranged hX ⁇ and unrearranged hJX are operably linked with a human or mouse ⁇ constant region ( ⁇ ).
  • a mouse comprises in its germline, at an endogenous mouse light chain locus, a human ⁇ light chain variable region sequence, wherein the human lambda variable region sequence is expressed in a light chain that comprises a mouse immunoglobulin constant region gene sequence.
  • the endogenous mouse light chain locus is a ⁇ locus. In one embodiment, the endogenous mouse light chain locus is a ⁇ locus.
  • the mouse lacks an endogenous light chain variable sequence at the endogenous mouse light chain locus.
  • all or substantially all endogenous mouse light chain variable region gene segments are replaced with one or more human ⁇ variable region gene segments.
  • the human ⁇ light chain variable region sequence comprises a human ⁇ sequence.
  • the human ⁇ sequence is selected from the group consisting of ⁇ 1 , ⁇ 2, ⁇ 3, JX7, and a combination thereof.
  • the human ⁇ light chain variable region sequence comprises a fragment of cluster A of the human light chain locus.
  • the fragment of cluster A of the human ⁇ light chain locus extends from hV 3- 27 through hV 3-1 .
  • the human ⁇ light chain variable region sequence comprises a fragment of cluster B of the human light chain locus.
  • the fragment of cluster B of the human ⁇ light chain locus extends from ⁇ 5- 52 through hVX1 -40.
  • the human ⁇ light chain variable region sequence comprises a genomic fragment of cluster A and a genomic fragment of cluster B. In a one embodiment, the human ⁇ light chain variable region sequence comprises at least one gene segment of cluster A and at least one gene segment of cluster B.
  • more than 10% of the light chain naive repertoire of the mouse is derived from at least two hN ⁇ gene segments selected from 2-8, 2-23, 1 -40, 5-45, and 9-49. In one embodiment, more than 20% of the light chain naive repertoire of the mouse is derived from at least three hX ⁇ gene segments selected from 2-8, 2-23, 1-40, 5- 45, and 9-49. In one embodiment, more than 30% of the light chain naive repertoire of the mouse is derived from at least four hV gene segments selected from 2-8, 2-23, 1 -40, 5- 45, and 9-49.
  • a mouse that expresses an immunoglobulin light chain that comprises a human ⁇ variable sequence fused with a mouse constant region, wherein the mouse exhibits a ⁇ usage to ⁇ usage ratio of about 1 :1.
  • the immunoglobulin light chain is expressed from an endogenous mouse light chain locus.
  • a mouse in one aspect, comprises a ⁇ light chain variable region sequence ( ⁇ ⁇ ) and at least one J sequence (J), contiguous with a mouse ⁇ light chain constant region sequence.
  • the mouse lacks a functional mouse VK and/or mouse JK gene segment.
  • the ⁇ ⁇ is a human ⁇ / ⁇ (hN/ ⁇ ), and the J is a human ⁇ (hJ ).
  • the hX ⁇ and the ⁇ are unrearranged gene segments.
  • the mouse comprises a plurality of unrearranged hN ⁇ gene segments and at least one hJk gene segment.
  • the plurality of unrearranged hN/ ⁇ gene segments are at least 12 gene segments, at least 28 gene segments, or at least 40 gene segments.
  • the at least one hJ gene segment is selected from the group consisting of ⁇ 1 , ⁇ 2, ⁇ 3, ⁇ 7, and a combination thereof.
  • an endogenous mouse ⁇ light chain locus is deleted in whole or in part.
  • the mouse ⁇ light chain constant region sequence is at an endogenous mouse ⁇ light chain locus.
  • about 10% to about 45% of the B cells of the mouse express an antibody that comprises a light chain comprising a human ⁇ light chain variable ( ⁇ / ⁇ ) domain and a mouse ⁇ light chain constant (CK) domain.
  • the human ⁇ variable domain is derived from a rearranged hVX/hJ sequence selected from the group consisting of 3-1/1 , 3-1/7, 4-3/1 , 4-3/7, 2-8/1 , 3- 9/1 , 3-10/1 , 3-10/3, 3-10/7, 2-14/1 , 3-19/1 , 2-23/1 , 3-25/1 , 1-40/1 , 1 -40/2, 1-40/3, 1-40/7, 7- 43/1 , 7-43/3, 1-44/1 , 1 -44/7, 5-45/1 , 5-45/2, 5-45/7, 7-46/1 , 7-46/2, 7-46/7, 9-49/1 , 9-49/2, 9-49/7 and 1 -51/1 .
  • the mouse further comprises a human VK-JK intergenic region from a human ⁇ light chain locus, wherein the human VK-JK intergenic region is contiguous with the VX sequence and the J sequence.
  • the human VK-JK intergenic region is placed between the VX sequence and the J sequence.
  • a mouse comprising (a) at least 12 to at least 40 unrearranged human ⁇ light chain variable region gene segments and at least one human JX gene segment at an endogenous mouse light chain locus; (b) a human VK-JK intergenic sequence located between the at least 12 to at least 40 human light chain variable region gene segments and the at least one human JX sequence; wherein the mouse express an antibody that comprises a light chain comprising a human ⁇ domain and a mouse CK domain.
  • a mouse that expresses an antibody comprising a light chain that comprises a ⁇ variable sequence and a ⁇ constant sequence.
  • the mouse exhibits a ⁇ usage to ⁇ usage ratio of about 1 : 1 .
  • a population of immature B cells obtained from bone marrow of the mouse exhibits a ⁇ usage to ⁇ usage ratio of about 1 : 1 .
  • a genetically modified mouse comprising an unrearranged immunoglobulin ⁇ and a JX gene segment operably linked to a mouse light chain locus that comprises a mouse CL gene.
  • the VX and/or JX gene segments are human gene segments.
  • the ⁇ and/or JX gene segments are mouse gene segments, and the C L is a mouse CK.
  • the endogenous mouse light chain locus is a ⁇ light chain locus. In one embodiment, the endogenous mouse light chain locus is a ⁇ light chain locus.
  • the unrearranged VX and JX gene segments are at an endogenous mouse light chain locus.
  • the unrearranged immunoglobulin ⁇ and JX gene segments are on a transgene.
  • the mouse further comprises a replacement of one or more heavy chain V, D, and/or J gene segments with one or more human V, D, and/or J gene segments at an endogenous mouse heavy chain immunoglobulin locus.
  • the mouse comprises an unrearranged immunoglobulin VX and a JX gene segment at an endogenous mouse ⁇ light chain locus that comprises a mouse CK gene.
  • the mouse comprises an unrearranged human
  • the light chain variable gene locus (the "V L locus") comprises at least one human VX (hVX) gene segment. In one embodiment, the V L locus comprises at least one human JX (hJX) gene segment. In another embodiment, V L locus comprises up to four hJX gene segments. In one embodiment, the V L locus comprises a contiguous sequence comprising human ⁇ and human ⁇ genomic sequence.
  • the ⁇ light chain variable gene locus (the " ⁇ locus") comprises at least one human VX (hVX) gene segment. In one embodiment, the ⁇ locus comprises at least one human ⁇ (hJX) gene segment. In one embodiment, the ⁇ locus comprises up to four hJX gene segments. In one embodiment, the ⁇ locus comprises at least one hVX and at least one hJX, and lacks or substantially lacks a functional VK region gene segment and lacks or substantially lacks a functional JK region gene segment. In one embodiment, the mouse comprises no functional VK region gene segment. In one embodiment, the mouse comprises no functional JK region gene segment.
  • the ⁇ light chain variable gene locus (the " ⁇ locus") comprises at least one hVX gene segment. In one embodiment, the ⁇ locus comprises at least one human JX (hJX) gene segment. In another embodiment, the X locus comprises up to four hJX gene segments.
  • the V L locus comprises a plurality of hVXs.
  • the plurality of hVXs are selected so as to result in expression of a X light chain variable region repertoire that reflects about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, or about 90% or more of the VX usage observed in a human.
  • the V L locus comprises gene segments hVX 1-40, 1-44, 2-8, 2-14, 3-21 , and a combination thereof.
  • the hVXs include 3-1 , 4-3, 2-8, 3-9, 3-10, 2-11 , and 3-12.
  • the V L locus comprises a contiguous sequence of the human X light chain locus that spans from VX3-12 to VX3-1.
  • the V L locus comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1 or 12 hVXs.
  • the hVXs include 3-1 , 4-3, 2-8, 3-9, 3-10, 2-1 1 , and 3-12.
  • the V L locus comprises a contiguous sequence of the human X locus that spans from VX3-12 to VX3-1.
  • the V L locus is at the endogenous ⁇ locus. In a specific embodiment, the V L locus is at the endogenous ⁇ locus and the endogenous X light chain locus is deleted in part or completely. In one embodiment, the V L locus is at the endogenous ⁇ locus. In a specific embodiment, the V L locus is at the endogenous ⁇ locus and the endogenous ⁇ locus is deleted in part or completely.
  • the V L locus comprises 13 to 28 or more hV s.
  • the hV s include 2-14, 3-16, 2-18, 3-19, 3-21 , 3-22, 2-23, 3-25, and 3-27.
  • the ⁇ locus comprises a contiguous sequence of the human ⁇ locus that spans from ⁇ -21 to ⁇ ⁇ 3-1.
  • the V L locus is at the endogenous ⁇ locus.
  • the V L locus is at the endogenous ⁇ locus and the endogenous ⁇ light chain locus is deleted in part or completely.
  • the V L locus is at the endogenous ⁇ locus.
  • the V L locus is at the endogenous ⁇ locus and the endogenous ⁇ locus is deleted in part or completely.
  • the VL locus comprises 29 to 40 hV s.
  • the ⁇ locus comprises a contiguous sequence of the human ⁇ locus that spans from ⁇ / ⁇ 3-29 to ⁇ / ⁇ 3-1 , and a contiguous sequence of the human ⁇ locus that spans from V 5-52 to ⁇ 1-40.
  • all or substantially all sequence between hV 1-40 and ⁇ / ⁇ 3-29 in the genetically modified mouse consists essentially of a human ⁇ sequence of approximately 959 bp found in nature (e.g., in the human population) downstream of the ⁇ / ⁇ 1-40 gene segment (downstream of the 3' untranslated portion), a restriction enzyme site (e.g., Pl-Scel), followed by a human ⁇ sequence of approximately 3,431 bp upstream of the hV 3-29 gene segment found in nature.
  • the V L locus is at the endogenous mouse ⁇ locus.
  • the V L locus is at the endogenous mouse ⁇ locus and the endogenous mouse ⁇ light chain locus is deleted in part or completely. In another embodiment, the V L locus is at the endogenous mouse ⁇ locus. In a specific embodiment, the V L locus is at the endogenous mouse ⁇ locus and the endogenous mouse ⁇ locus is deleted in part or completely.
  • the V L locus comprises at least one hJ . In one embodiment, the V L locus comprises at least one hJ .
  • the V L locus comprises a plurality of hJ s. In one embodiment, the V L locus comprises at least 2, 3, 4, 5, 6, or 7 hJX. In a specific embodiment, the V L locus comprises four hJ . In a specific embodiment, the four hJ s are ⁇ , hJ 2, hJX3, and ⁇ 7. In one embodiment, the V L locus is a ⁇ locus. In a specific embodiment, the V L locus is at the endogenous ⁇ locus and the endogenous ⁇ light chain locus is deleted in part or completely. In one embodiment, the V L locus comprises one hJX. In a specific
  • the one hJ is hJ 1 .
  • the V L locus is at the endogenous K locus. In a specific embodiment, the V L locus is at the endogenous locus and the endogenous ⁇ light chain locus is deleted in part or completely. In another embodiment, the V L locus is at the endogenous ⁇ locus. In a specific embodiment, the V L locus is at the endogenous ⁇ locus and the endogenous ⁇ locus is deleted in part or completely.
  • the V L locus comprises at least one hN ⁇ , at least one bJk, and a mouse CK gene. In one embodiment, the V L locus comprises at least one h ⁇ A,, at least one hJ , and a mouse Ck gene. In a specific embodiment, the mouse Ck gene is Ck2. In a specific embodiment, the mouse Ck gene is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, 96%, 97%, 98%, or at least 99% identical to mouse Ck2.
  • the mouse comprises a replacement at the endogenous mouse K locus of endogenous mouse VK gene segments with one or more hVX gene segments, wherein the hV gene segments are operably linked to an endogenous mouse CK region gene, such that the mouse rearranges the human ⁇ gene segments and expresses a reverse chimeric immunoglobulin light chain that comprises a human ⁇ domain and a mouse CK.
  • 90-100% of unrearranged mouse VK gene segments are replaced with at least one unrearranged hN/ ⁇ gene segment.
  • all or substantially all of the endogenous mouse VK gene segments are replaced with at least one unrearranged hV gene segment.
  • the replacement is with at least 12, at least 28, or at least 40 unrearranged hV gene segments. In one embodiment, the replacement is with at least 7 functional unrearranged hV gene segments, at least 16 functional unrearranged hV gene segments, or at least 27 functional unrearranged hVk gene segments. In one embodiment, the mouse comprises a replacement of all mouse JK gene segments with at least one unrearranged hJX gene segment. In one embodiment, the at least one unrearranged bJk gene segment is selected from ⁇ 1 , Jk2, J 3, ⁇ 4, ⁇ 5, ⁇ 6, JX7, and a combination thereof.
  • the one or more A ⁇ gene segment is selected from a 3-1 , 4-3, 2-8, 3-9, 3- 10, 2-11 , 3-12, 2-14, 3-16, 2-18, 3-19, 3-21 , 3-22, 2-23, 3-25, 3-27, 1-40, 7-43, 1 -44, 5-45, 7-46, 1-47, 5-48, 9-49, 1 -50, 1 -51 , a 5-52 hV gene segment, and a combination thereof.
  • the at least one unrearranged ⁇ gene segment is selected from ⁇ 1 , ⁇ 2, ⁇ 3, ⁇ 7, and a combination thereof.
  • the mouse comprises a replacement of endogenous mouse ⁇ gene segments at the endogenous mouse ⁇ locus with one or more human ⁇ gene segments at the endogenous mouse ⁇ locus, wherein the hVk gene segments are operably linked to a mouse Ck region gene, such that the mouse rearranges the hVX gene segments and expresses a reverse chimeric immunoglobulin light chain that comprises a hVX domain and a mouse Ck.
  • the mouse Ck gene is Ck2.
  • the mouse Ck gene is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse C 2.
  • 90- 100% of unrearranged mouse ⁇ gene segments are replaced with at least one
  • unrearranged hX ⁇ gene segment In a specific embodiment, all or substantially all of the endogenous mouse ⁇ gene segments are replaced with at least one unrearranged hX ⁇ gene segment. In one embodiment, the replacement is with at least 12, at least 28, or at least 40 unrearranged hN ⁇ gene segments. In one embodiment, the replacement is with at least 7 functional unrearranged hN ⁇ gene segments, at least 16 functional unrearranged hN/ ⁇ gene segments, or at least 27 functional unrearranged hVX gene segments. In one embodiment, the mouse comprises a replacement of all mouse ⁇ gene segments with at least one unrearranged hJ gene segment.
  • the at least one unrearranged ⁇ gene segment is selected from ⁇ 1 , ⁇ 2, JX3, ⁇ 4, ⁇ 5, ⁇ , ⁇ 7, and a combination thereof.
  • the one or more hN/ ⁇ gene segment is selected from a 3-1 , 4-3, 2-8, 3-9, 3-10, 2-1 1 , 3-12, 2-14, 3-16, 2-18, 3-19, 3-21 , 3-22, 2- 23, 3-25, 3-27, 1 -40, 7-43, 1 -44, 5-45, 7-46, 1 -47, 5-48, 9-49, 1 -50, 1 -51 , a 5-52 hV gene segment, and a combination thereof.
  • the at least one or more hN/ ⁇ gene segment is selected from a 3-1 , 4-3, 2-8, 3-9, 3-10, 2-1 1 , 3-12, 2-14, 3-16, 2-18, 3-19, 3-21 , 3-22, 2- 23, 3-25, 3-27, 1 -40, 7-43, 1 -44
  • unrearranged hJ gene segment is selected from ⁇ 1 , JX2, JX3, ⁇ 7, and a combination thereof.
  • a genetically modified mouse that comprises a human VK-JK intergenic region sequence located at an endogenous mouse ⁇ light chain locus.
  • the human VK-JK intergenic region sequence is at an endogenous ⁇ light chain locus of a mouse that comprises a hX ⁇ and hJ gene segment, and the human VK-JK intergenic region sequence is disposed between the hV and hJ gene segments.
  • the hA/ ⁇ and hJ gene segments are capable of recombining to form a functional human ⁇ light chain variable domain in the mouse.
  • a mouse comprising a plurality of hV 's and one or more J 's, and the human VK-JK intergenic region sequence is disposed, with respect to transcription, downstream of the proximal or 3' most hV sequence and upstream or 5' of the first J sequence.
  • the human VK-JK intergenic region is a region located about 130 bp downstream or 3' of a human VK4-1 gene segment, about 130 bp
  • the human VK-JK intergenic region is about 22.8 kb in size. In one embodiment, the VK-JK intergenic region is about 90% or more, 91 % or more, 92% or more, 93% or more, 94% or more, or about 95% or more identical with a human VK-JK intergenic region extending from the end of the 3' untranslated region of a human VK4-1 gene segment to about 600 bp upstream of a human JK1 gene segment.
  • the VK-JK intergenic region comprises SEQ ID NO: 1 00. In a specific embodiment, the VK-JK intergenic region comprises a functional fragment of SEQ ID NO: 100. In a specific embodiment, the VK-JK intergenic region is SEQ ID NO: 1 00.
  • a mouse, a mouse cell e.g., a mouse embryonic stem cell
  • a mouse embryo e.g., a mouse embryo, and a mouse tissue
  • the ectopic sequence is placed at a humanized endogenous mouse immunoglobulin locus.
  • an isolated nucleic acid construct comprising the recited human VK-JK intergenic region sequence.
  • the nucleic acid construct comprises targeting arms to target the human VK-JK intergenic region sequence to a mouse light chain locus.
  • the mouse light chain locus is a ⁇ locus.
  • the targeting arms target the human VK-JK intergenic region to a modified endogenous mouse ⁇ locus, wherein the targeting is to a position between a hV sequence and a hJ sequence.
  • a genetically modified mouse comprising no more than two light chain alleles, wherein the light chain alleles comprise (a) an unrearranged immunoglobulin human V and a JX gene segment at an endogenous mouse light chain locus that comprises a mouse C L gene; and, (b) an unrearranged immunoglobulin V L and a J L gene segment at an endogenous mouse light chain locus that comprises a mouse CL gene.
  • the endogenous mouse light chain locus is a ⁇ locus. In another embodiment, the endogenous mouse light chain locus is a ⁇ locus.
  • the no more than two light chain alleles are selected from a
  • one of the two light chain alleles is a ⁇ allele that comprises a 0 2 gene.
  • the mouse comprises one functional immunoglobulin light chain locus and one nonfunctional light chain locus, wherein the functional light chain locus comprises an unrearranged immunoglobulin human ⁇ and a gene segment at an endogenous mouse ⁇ light chain locus that comprises a mouse CK gene.
  • the mouse comprises one functional immunoglobulin light chain locus and one nonfunctional light chain locus, wherein the functional light chain locus comprises an unrearranged immunoglobulin human ⁇ and a ⁇ gene segment at an endogenous mouse ⁇ light chain locus that comprises a mouse CX gene.
  • the CX gene is CX2.
  • the mouse CX gene is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse CX2.
  • the mouse further comprises at least one immunoglobulin heavy chain allele.
  • the at least one immunoglobulin heavy chain allele comprises a human V H gene segment, a human D H gene segment, and a human J H gene segment at an endogenous mouse heavy chain locus that comprises a human heavy chain gene that expresses a human/mouse heavy chain.
  • the mouse comprises two immunoglobulin heavy chain alleles, and the mouse expresses a human/mouse heavy chain.
  • the mouse comprises a first light chain allele that comprises an unrearranged h and an unrearranged hJi , at an endogenous mouse ⁇ locus that comprises an endogenous CK gene; and a second light chain allele that comprises an unrearranged hVX and an unrearranged hJX, at an endogenous mouse ⁇ locus that comprises an endogenous CK gene.
  • the first and the second light chain alleles are the only functional light chain alleles of the genetically modified mouse.
  • the mouse comprises a nonfunctional ⁇ locus.
  • the genetically modified mouse does not express a light chain that comprises a ⁇ constant region.
  • the mouse comprises a first light chain allele that comprises an unrearranged h and an unrearranged hJK, at an endogenous mouse ⁇ locus that comprises an endogenous CK gene; and a second light chain allele that comprises an unrearranged hVX and an unrearranged hJX, at an endogenous mouse ⁇ locus that comprises an endogenous CX gene.
  • the first and the second light chain alleles are the only functional light chain alleles of the genetically modified mouse.
  • the endogenous CX gene is CX2.
  • the mouse CX gene is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse CX2.
  • the mouse comprises six immunoglobulin alleles, wherein the first allele comprises an unrearranged immunoglobulin VX and JX gene segment at an endogenous mouse ⁇ light chain locus that comprises a mouse CK gene, the second comprises an unrearranged immunoglobulin VK and JK gene segment at an endogenous mouse ⁇ light chain locus that comprises a mouse CK gene, the third comprises an unrearranged immunoglobulin VX and JX gene segment at an endogenous mouse ⁇ light chain locus that comprises a mouse CX gene, the fourth and fifth each independently comprise an unrearranged V H and D H and J H gene segment at an endogenous mouse heavy chain locus that comprises a mouse heavy chain gene, and the sixth comprises either (a) an unrearranged immunoglobulin VX and JX gene segment at an endogenous mouse ⁇ light chain locus that comprises a mouse CX gene, (b) a ⁇ locus that is nonfunctional, or (c) a deletion in whole or in part of the ⁇
  • the first allele comprises an unrearranged VX and hJX.
  • the second allele comprises an unrearranged h and hJi .
  • the third allele comprises an unrearranged hX ⁇ and hJX. In one
  • the fourth and fifth each independently comprise an unrearranged hV H and hD H and hJ H .
  • the sixth allele comprises an endogenous mouse ⁇ locus that is deleted in whole or in part.
  • the mouse comprises six immunoglobulin alleles, wherein the first allele comprises an unrearranged immunoglobulin ⁇ / ⁇ and ⁇ gene segment at an endogenous mouse ⁇ light chain locus that comprises a mouse CX gene, the second comprises an unrearranged immumoglobulin ⁇ / ⁇ and ⁇ gene segment at an endogenous mouse ⁇ light chain locus that comprises a mouse CX gene, the third comprises an unrearranged immunoglobulin V and JK gene segment at an endogenous mouse ⁇ light chain locus that comprises a mouse CK gene, the fourth and fifth each independently comprise an unrearranged V H and D H and J H gene segment at an endogenous mouse heavy chain locus that comprises a mouse heavy chain gene, and the sixth comprises either (a) an unrearranged immunoglobulin VK and JK gene segment at an endogenous mouse K light chain locus that comprises a mouse CK gene, (b) a ⁇ locus that is nonfunctional, or (c) a deletion of one or more
  • the first allele comprises an unrearranged hN ⁇ and hJX gene segment.
  • the second allele comprises an unrearranged hVX and hJX gene segment.
  • the third allele comprises an unrearranged hN/ ⁇ and hJK gene segment.
  • the fourth and fifth each independently comprise an unrearranged hV H and hD H and hJ H gene segment.
  • the sixth allele comprises an endogenous mouse ⁇ locus that is functionally silenced.
  • the genetically modified mouse comprises a B cell that comprises a rearranged antibody gene comprising a rearranged h ⁇ A. domain operably linked to a mouse C L domain.
  • the mouse C L domain is selected from a mouse CK and a mouse CX domain.
  • the mouse CX domain is derived from a CX2 gene.
  • the mouse CX domain is derived from a C domain that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse C 2.
  • a genetically modified mouse that expresses a ⁇ region on a C L that is a CK. In one aspect, a genetically modified mouse is provided that expresses a hVX region on a C L selected from a human CK, a human C , or a mouse CK. In one aspect, a genetically modified mouse is provided that expresses a h ⁇ A. region on a mouse CK.
  • splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 9-28% express an immunoglobulin light chain comprising a hV domain fused to a mouse CK domain.
  • the splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 9-1 1 % express an immunoglobulin light chain comprising a hN ⁇ domain fused to a mouse CK domain.
  • the splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 9-17% express an immunoglobulin light chain comprising a hN/ ⁇ domain fused to a mouse CK domain.
  • the splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 24-27% express an immunoglobulin light chain comprising a hN ⁇ domain fused to a mouse CK domain.
  • splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 9-13% express an immunoglobulin light chain comprising a hV domain fused to a mouse CK domain.
  • the splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 15-21 % express an immunoglobulin light chain comprising a hV domain fused to a mouse CK domain.
  • about 30-38% of the splenocytes of the mouse are B cells (i.e., CD19-positive), of which about 33-48% express an immunoglobulin light chain comprising a hVX domain fused to a mouse CK domain.
  • about 52-70% of the bone marrow of the mouse are B cells (i.e., CD19-positive), or which about 31 -47% of the immature B cells (i.e. , CD19- positive/B220-intermediate positive/lgM-positive) express an immunoglobulin light chain comprising a h ⁇ A. domain fused to a mouse CK domain.
  • B cells i.e., CD19-positive
  • immature B cells i.e. , CD19- positive/B220-intermediate positive/lgM-positive
  • the mouse expresses an antibody comprising a light chain that comprises a variable domain derived from a human V and a human J gene segment, and a constant domain derived from a mouse constant region gene.
  • the mouse constant region gene is a CK gene.
  • the mouse constant region gene is a CX gene.
  • the CX region is CX2.
  • the mouse CX gene is derived from a CX gene that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse CX2.
  • the antibody further comprises a heavy chain comprising a variable domain derived from a human V, a human D and a human J gene segment, and a heavy chain constant domain derived from a mouse heavy chain constant region gene.
  • the mouse heavy chain constant region gene comprises a hinge-CH 2 - CH 3 sequence of a heavy chain constant domain.
  • the mouse heavy chain constant region gene comprises a CH 1 -hinge-CH 2 -CH 3 sequence of a heavy chain constant domain. In another embodiment, the mouse heavy chain constant region gene comprises a CH CH 2 -CH3-CH4 sequence of a heavy chain constant domain. In another embodiment, the mouse heavy chain constant region gene comprises a CH 2 -CH 3 - CH 4 sequence of a heavy chain constant domain.
  • the mouse expresses an antibody comprising a light chain that comprises a rearranged human VX-JX sequence and a mouse CK sequence.
  • the rearranged human ⁇ / ⁇ - ⁇ sequence is derived from a rearrangement of hX ⁇ gene segments selected from a 3-1 , 4-3, 2-8, 3-9, 3-10, 2-14, 3-19, 2-23, 3-25, 1 -40, 7-43, 1 -44, 5-45, 7-46, 1 -47, 9-49, and a 1 -51 gene segment.
  • the rearranged human ⁇ / ⁇ - ⁇ sequence is derived from a rearrangement of ⁇ gene segments selected from JX1 , JX2, ⁇ 3, and a JX7 gene segment.
  • the mouse expresses an antibody comprising a light chain that comprises a rearranged immunoglobulin ⁇ light chain variable region comprising a human ⁇ / ⁇ sequence selected from 3-1 /1 , 3-1/7, 4-3/1 , 4-3/7, 2-8/1 , 3-9/1 , 3-10/1 , 3- 10/3, 3-10/7, 2-14/1 , 3-19/1 , 2-23/1 , 3-25/1 , 1 -40/1 , 1 -40/2, 1 -40/3, 1 -40/7, 7-43/1 , 7-43/3, 1 -44/1 , 1 -44/7, 5-45/1 , 5-45/2, 5-45/7, 7-46/1 , 7-46/2, 7-46/7, 9-49/1 , 9-49/2, 9-49/7 and 1 - 51 /1 .
  • the B cell expresses an antibody comprising a human immunoglobulin heavy chain variable domain fused with a mouse heavy chain constant domain, and a human immunoglobulin ⁇ light chain variable domain fused with a mouse ⁇ light chain constant domain.
  • a mouse that expresses an antibody comprising (a) a heavy chain comprising a heavy chain variable domain derived from an unrearranged human heavy chain variable region gene segment, wherein the heavy chain variable domain is fused to a mouse heavy chain constant (C H ) region; and, (b) a light chain comprising a light chain variable domain derived from an unrearranged hN ⁇ and a Jk, wherein the light chain variable domain is fused to a mouse CL region.
  • C H mouse heavy chain constant
  • the mouse comprises (i) a heavy chain locus that comprises a replacement of all or substantially all functional endogenous mouse V, D and J gene segments with all or substantially all functional human V, D, and J gene segments, a mouse C H gene, (ii) a first ⁇ light chain locus comprising a replacement of all or substantially all functional endogenous mouse VK and JK gene segments with all, substantially all, or a plurality of, functional hN ⁇ and hJX gene segments, and a mouse CK gene, (iii) a second ⁇ light chain locus comprising a replacement of all or substantially all functional endogenous mouse VK and JK gene segments with all, substantially all, or a plurality of, functional hN/ ⁇ and ⁇ gene segments, and a mouse CK gene.
  • the mouse does not express an antibody that comprises a Ck region.
  • the mouse comprises a deletion of a C gene and/or a ⁇ and/or a ⁇ gene segment.
  • the mouse comprises a nonfunctional ⁇ light chain locus.
  • the ⁇ light chain locus is deleted in whole or in part.
  • the mouse comprises (i) a heavy chain locus that comprises a replacement of all or substantially all functional endogenous mouse V, D and J gene segments with all or substantially all functional human V, D, and J gene segments, a mouse C H gene, (ii) a first ⁇ light chain locus comprising a replacement of all or substantially all functional endogenous mouse Vk and Jk gene segments with all, substantially all, or a plurality of, functional hN/ ⁇ and hJk gene segments, and a mouse Ck gene, (iii) a second ⁇ light chain locus comprising a replacement of all or substantially all functional endogenous mouse ⁇ and ⁇ gene segments with all, substantially all, or a plurality of, functional hN ⁇ and hJX gene segments, and a mouse Ck gene.
  • the mouse Ck gene is Ck2. In a specific embodiment, the mouse Ck gene is derived from a Ck gene that is at least 60%, at least 70%, at least 80% , at least 90%, at least 95% , or at least 98% identical to mouse C 2.
  • the mouse comprises a deletion of a CK gene and/or a VK and/or a JK gene segment. In one embodiment, the mouse comprises a nonfunctional ⁇ light chain locus.
  • a genetically modified mouse that expresses an antibody
  • greater than 1 0%, greater than 1 5%, greater than 20%, greater than 25%, greater than 30%, greater than 35% , greater than 40%, greater than 60%, greater than 70% , greater than 80% , or greater than 90% of total IgG antibody produced by the mouse comprises a ⁇ -derived variable domain
  • the mouse expresses antibodies comprising a ⁇ -derived variable domain fused with a mouse CK region.
  • about 15-40%, 20-40%, 25-40%, 30-40%, or 35-40% of total antibody produced by the mouse comprises a ⁇ -derived variable domain.
  • the ⁇ -derived variable domain is derived from a hX ⁇ and a hJ .
  • the ⁇ -derived variable domain is in a light chain that comprises a mouse CK region.
  • the ⁇ -derived variable region is in a light chain that comprises a mouse C region.
  • the Ck region is a ⁇ 2 region.
  • the ⁇ -derived variable domain is derived from a hN ⁇ and a ⁇ , and in a specific embodiment is in a light chain that comprises a mouse CK region.
  • an isolated DNA construct comprising an upstream homology arm and a downstream homology arm, wherein the upstream and the downstream homology arms target the construct to a mouse ⁇ locus, and the construct comprises a functional unrearranged hVX segment and a functional unrearranged hJ segment, and a selection or marker sequence.
  • an isolated DNA construct comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting a mouse ⁇ sequence upstream of mouse ⁇ ZX2, a selection cassette flanked 5' and 3' with recombinase recognition sites, and a targeting arm for targeting a mouse ⁇ sequence 3' of mouse ⁇ 2.
  • the selection cassette is a Fifed Hyg-TK cassette.
  • the 3' targeting arm comprises mouse CX2, JX4, C 4, and mouse enhancer 2.4.
  • an isolated DNA construct comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse ⁇ locus 5' with respect to ⁇ ⁇ 1 , a selection cassette flanked 5' and 3' with recombinase recognition sites, and a 3' targeting arm for targeting a mouse ⁇ sequence 3' with respect to mouse C 1 .
  • the selection cassette is a loxed neomycin cassette.
  • the 3' targeting arm comprises the mouse ⁇ 3' enhancer and mouse ⁇ 3' enhancer 3.1 .
  • an isolated DNA construct comprising from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse ⁇ locus 5' with respect to ⁇ ⁇ 2, a selection cassette flanked 5' and 3' with recombinase recognition sites, and a 3' targeting arm for targeting a mouse ⁇ sequence 3' with respect to mouse ⁇ 2 and 5' with respect to mouse CX2.
  • the selection cassette is a Fifed hygromycin-TK cassette.
  • the 3' targeting arm comprises the mouse C 2-JX4-C 4 gene segments and mouse ⁇ enhancer 2.4.
  • an isolated DNA construct comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse ⁇ locus 5' with respect to ⁇ / ⁇ 2, a selection cassette flanked 5' and 3' with recombinase recognition sites, a human genomic fragment comprising a contiguous region of the human ⁇ light chain locus from h ⁇ A.3-12 downstream to the end of hJ 1 , and a 3' targeting arm for targeting a mouse ⁇ sequence 3' with respect to mouse ⁇ 2.
  • the selection cassette is a Fifed neomycin cassette.
  • the 3' targeting arm comprises the mouse ⁇ 2- ⁇ 4- ⁇ 4 gene segments and mouse ⁇ enhancer 2.4.
  • an isolated DNA construct comprising a contiguous region of the human ⁇ light chain locus from hV 3-12 downstream to the end of hJ 1.
  • an isolated DNA construct comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse ⁇ locus 5' with respect to ⁇ 2, a selection cassette flanked 5' and 3' with recombinase recognition sites and a human genomic fragment comprising a contiguous region of the human ⁇ light chain locus from hV 3-27 downstream to the end of hV 2-8.
  • the selection cassette is a Fifed hygromycin cassette.
  • the human genomic fragment comprises a 3' targeting arm.
  • the 3' targeting arm comprises about 53 kb of the human ⁇ light chain locus from hVX3-12 downstream to the end of hV 2-8.
  • an isolated DNA construct comprising a contiguous region of the human ⁇ light chain locus from hV 3-27 downstream to the end of hV 3-12.
  • an isolated DNA construct comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse ⁇ locus 5' with respect to ⁇ / ⁇ 2, a selection cassette flanked 5' and 3' with recombinase recognition sites, a first human genomic fragment comprising a contiguous region of the human ⁇ light chain locus from h ⁇ A5-52 downstream to the end of h ⁇ A.1-40, a restriction enzyme site, and a second human genomic fragment comprising a contiguous region of the human ⁇ light chain locus from h ⁇ A.3-29 downstream to the end of hVX82K.
  • the selection cassette is a Fi ed neomycin cassette.
  • the restriction enzyme site is a site for a homing endonuclease.
  • the homing endonuclease is Pl-Scel.
  • the second human genomic fragment is a 3' targeting arm.
  • the 3' targeting arm comprises about 27 kb of the human ⁇ light chain locus from hV 3-29 downstream to the end of hV 82K.
  • an isolated DNA construct is provided, comprising a contiguous region of the human ⁇ light chain locus from hV 5-52 downstream to the end of hV 1 -40.
  • an isolated DNA construct comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse ⁇ locus 5' with respect to the endogenous VK gene segments, two juxtaposed recombinase recognition sites, a selection cassette 3' to the juxtaposed recombinase recognition sites, and a 3' targeting arm for targeting a mouse ⁇ sequence 5' with respect to the ⁇ light chain variable gene segments.
  • the juxtaposed recombinase recognition sites are in opposite orientation with respect to one another.
  • the recombinase recognition sites are different.
  • the recombinase recognition sites are a loxP site and a /ox511 site.
  • the selection cassette is a neomycin cassette.
  • an isolated DNA construct comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse ⁇ locus 5' with respect to the mouse JK gene segments, a selection cassette, a recombinase recognition site 3' to the selection cassette, and a 3' targeting arm for targeting a mouse ⁇ sequence 3' with respect to the mouse JK gene segments and 5' to the mouse ⁇ intronic enhancer.
  • the selection cassette is a hygromycin-TK cassette.
  • the recombinase recognition site is in the same direction with respect to transcription as the selection cassette.
  • the recombinase recognition site is a loxP site.
  • an isolated DNA construct comprising, from 5' to 3' with respect to the direction of transcription, a first mouse genomic fragment comprising sequence 5' of the endogenous mouse VK gene segments, a first recombinase recognition site, a second recombinase recognition site, and a second mouse genomic fragment comprising sequence 3' of the endogenous mouse JK gene segments and 5' of the mouse ⁇ intronic enhancer.
  • a genetically modified mouse wherein the genetic modification comprises a modification with one or more of the DNA constructs described above or herein.
  • use of an isolated DNA construct to make a mouse as described herein is provided.
  • use of an isolated DNA construct as described herein in a method for making an antigen-binding protein is provided.
  • a non-human stem cell that comprises a targeting vector that comprises a DNA construct as described above and herein.
  • a non-human stem cell is provided, wherein the non-human stem cell is derived from a mouse described herein.
  • the non-human stem cell is an embryonic stem (ES) cell.
  • the ES cell is a mouse ES cell.
  • use of a non-human stem cell as described herein to make a mouse as described herein is provided. In one aspect, use of a non-human stem cell as described herein to make an antigen-binding protein is provided.
  • a mouse embryo comprising a genetic modification as provided herein.
  • a host mouse embryo that comprises a donor ES cell is provided, wherein the donor ES cell comprises a genetic modification as described herein.
  • the mouse embryo is a pre- morula stage embryo.
  • the pre-morula stage embryo is a 4-cell stage embryo or an 8-cell stage embryo.
  • the mouse embryo is a blastocyst.
  • a mouse embryo as described herein to make a mouse as described herein is provided. In one aspect, use of a mouse embryo as described herein to make an antigen-binding protein is provided.
  • a non-human cell comprising a rearranged immunoglobulin light chain gene sequence derived from a genetically modified mouse as described herein.
  • the cell is a B cell.
  • the cell is a hybridoma.
  • the cell encodes an immunoglobulin light chain variable domain and/or an immunoglobulin heavy chain variable domain that is somatically mutated.
  • a non-human cell comprising a rearranged immunoglobulin light chain gene sequence derived from a genetically modified mouse as described herein.
  • the cell is a B cell.
  • the cell is a hybridoma.
  • the cell encodes an immunoglobulin light chain variable domain and/or an immunoglobulin heavy chain variable domain that is somatically mutated.
  • use of a non-human cell as described herein to make a mouse as described herein is provided. In one aspect, use of a non-human cell as described herein to make an antigen-binding protein is provided.
  • a mouse B cell that expresses an immunoglobulin light chain that comprises (a) a variable region derived from a hX ⁇ gene segment and a bJ gene segment; and, (b) a mouse C L gene.
  • the mouse C L gene is selected from a CK and a CX gene.
  • the Ck gene is C 2.
  • the mouse C gene is derived from a C gene that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse C 2.
  • the mouse B cell further expresses a cognate heavy chain that comprises (c) a variable region derived from a hV H , a hD H , and (d) a hJ H segment.
  • the B cell does not comprise a rearranged ⁇ gene. In another embodiment, the B cell does not comprise a rearranged ⁇ gene.
  • a method for making an antibody in a genetically modified mouse comprising: (a) exposing a genetically modified mouse to an antigen, wherein the mouse has a genome comprising at least one hX ⁇ and at least one hJ at an endogenous light chain locus, wherein the endogenous light chain locus comprises a mouse C L gene; (b) allowing the genetically modified mouse to develop an immune response to the antigen; and, (c) isolating from the mouse of (b) an antibody that specifically recognizes the antigen, or isolating from the mouse of (b) a cell comprising an immunoglobulin domain that specifically recognizes the antigen, wherein the antibody comprises a light chain derived from a hN ⁇ , a hJX and a mouse C L gene.
  • the mouse C L gene is a mouse CK gene.
  • a method for making an antibody in a genetically modified mouse comprising: (a) exposing a genetically modified mouse to an antigen, wherein the mouse has a genome comprising at least one hX ⁇ at an endogenous ⁇ locus and at least one hJ at the ⁇ locus, wherein the ⁇ locus comprises a mouse CK gene; (b) allowing the genetically modified mouse to develop an immune response to the antigen; and, (c) isolating from the mouse of (b) an antibody that specifically recognizes the antigen, or isolating from the mouse of (b) a cell comprising an immunoglobulin domain that specifically recognizes the antigen, wherein the antibody comprises a light chain derived from a hN/ ⁇ , a ⁇ and a mouse CK gene.
  • the ⁇ light chain constant gene is selected from a human CK gene and a mouse CK gene.
  • a method for making an antibody in a genetically modified mouse comprising: (a) exposing a genetically modified mouse to an antigen, wherein the mouse has a genome comprising at least one hN/ ⁇ at a ⁇ light chain locus and at least one ⁇ at the ⁇ light chain locus, wherein the ⁇ light chain locus comprises a mouse CK gene; (b) allowing the genetically modified mouse to develop an immune response to the antigen; and, (c) isolating from the mouse of (b) an antibody that specifically recognizes the antigen, or isolating from the mouse of (b) a cell comprising an immunoglobulin domain that specifically recognizes the antigen, or identifying in the mouse of B a nucleic acid sequence encoding a heavy and/or light chain variable domain that binds the antigen, wherein the antibody comprises a light chain derived from a hN/ ⁇ , a hJ and a mouse Ck gene.
  • the ⁇ light chain constant gene is selected from a human CK gene and a mouse Ck gene.
  • the ⁇ light chain constant gene is a human Ck gene.
  • the human Ck gene is selected from ⁇ 1 , Ck2, Ck3 and Ckl.
  • the ⁇ light chain constant gene is a mouse Ck gene.
  • the mouse Ck gene is selected from C 1 , Ckl and CK2>.
  • the mouse Ck gene is Ckl.
  • the mouse Ck gene is derived from a Ck gene that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse Ckl.
  • a method for making a rearranged antibody gene in a genetically modified mouse comprising: (a) exposing a genetically modified mouse to an antigen, wherein the genetic modification comprises a YNK and a hJ at an endogenous light chain locus, wherein the endogenous light chain locus comprises a mouse C L gene or functional fragment thereof; and, (b) identifying a rearranged immunoglobulin gene in said mouse, wherein the rearranged immunoglobulin gene comprises a ⁇ light chain variable region gene segment and a CL gene or functional fragment thereof.
  • the method further comprises cloning a nucleic acid sequence encoding a heavy and/or light chain variable region from the mouse, wherein the heavy and/or light chain variable region is from an antibody that comprises a human k and a mouse C L .
  • the mouse C L gene or functional fragment thereof is selected from a human C L gene and a mouse C L gene, or functional fragment thereof.
  • a method for making a rearranged antibody gene in a genetically modified mouse comprising: (a) exposing a genetically modified mouse to an antigen, wherein the genetic modification comprises a Vk and a hJk at a ⁇ light chain locus, wherein the ⁇ light chain locus comprises a mouse CK gene or functional fragment thereof; and, (b) identifying a rearranged immunoglobulin gene in said mouse, wherein the rearranged immunoglobulin gene comprises a ⁇ light chain variable region gene segment and a CK gene or functional fragment thereof.
  • the ⁇ light chain constant gene or functional fragment thereof is selected from a human CK gene and a mouse CK gene, or a functional fragment thereof.
  • the method further comprises cloning a nucleic acid sequence encoding a heavy and/or light chain variable region from the mouse, wherein the heavy and/or light chain variable region is from an antibody that comprises a human VX and a mouse CK,
  • a method for making a rearranged antibody gene in a genetically modified mouse comprising: (a) exposing a genetically modified mouse to an antigen, wherein the genetic modification comprises a hVX and a hJX at a mouse ⁇ light chain locus, wherein the ⁇ light chain locus comprises a mouse CX gene or functional fragment thereof; and, (b) identifying a rearranged immunoglobulin gene in said mouse, wherein the rearranged immunoglobulin gene comprises a ⁇ light chain variable region gene segment and a CX gene or functional fragment thereof.
  • the ⁇ light chain constant gene or functional fragment thereof is selected from a human CX gene and a mouse CX gene, or a functional fragment thereof.
  • the ⁇ light chain constant gene is a mouse CX gene, or a functional fragment thereof.
  • the method further comprises cloning a nucleic acid sequence encoding a heavy and/or light chain variable region from the mouse, wherein the heavy and/or light chain variable region is from an antibody that comprises a human VX and a mouse CX.
  • a method for making an antibody comprising exposing a mouse as described herein to an antigen, allowing the mouse to mount an immune response that comprises making an antibody that specifically binds the antigen, identifying a rearranged nucleic acid sequence in the mouse that encodes heavy chain and a rearranged nucleic acid sequence in the mouse that encodes a cognate light chain variable domain sequence of an antibody, wherein the antibody specifically binds the antigen, and employing the nucleic acid sequences of the heavy and light chain variable domains fused to human constant domains to make a desired antibody, wherein the desired antibody comprises a light chain that comprises a VX domain fused to a C L domain.
  • the VX domain is human and the CL domain is a human or mouse CX domain.
  • the VX domain is mouse and the C L domain is a human or mouse CK domain.
  • a method for making an antibody comprising exposing a mouse as described herein to an antigen, allowing the mouse to mount an immune response that comprises making an antibody that specifically binds the antigen, identifying a rearranged nucleic acid sequence in the mouse that encodes a heavy chain and a rearranged nucleic acid sequence in the mouse that encodes a cognate light chain variable domain sequence of an antibody, wherein the antibody specifically binds the antigen, and employing the nucleic acid sequences of the heavy and light chain variable domains fused to nucleic acid sequences of human constant domains to make a desired antibody, wherein the desired antibody comprises a light chain that comprises a ⁇ / ⁇ domain fused to a CK domain.
  • a method for making an antibody comprising exposing a mouse as described herein to an antigen, allowing the mouse to mount an immune response that comprises making an antibody that specifically binds the antigen, identifying a rearranged nucleic acid sequence in the mouse that encodes a heavy chain variable domain and a rearranged nucleic acid sequence that encodes a cognate light chain variable domain sequence of an antibody, wherein the antibody specifically binds the antigen, and employing the nucleic acid sequences fused to nucleic acid sequences that encode a human heavy chain constant domain and a human light chain constant domain to make an antibody derived from human sequences, wherein the antibody that specifically binds the antigen comprises a light chain that comprises a human ⁇ domain fused to a mouse CX region.
  • the mouse C region is selected from ⁇ 1 , ⁇ 2 and ⁇ 3. In a specific embodiment, the mouse Ck region is ⁇ 2.
  • a method for making a rearranged antibody light chain variable region gene sequence comprising (a) exposing a mouse as described herein to an antigen; (b) allowing the mouse to mount an immune response; (c) identifying a cell in the mouse that comprises a nucleic acid sequence that encodes a rearranged human ⁇ / ⁇ domain sequence fused with a mouse CL domain, wherein the cell also encodes a cognate heavy chain comprising a human V H domain and a mouse C H domain, and wherein the cell expresses an antibody that binds the antigen; (d) cloning from the cell a nucleic acid sequence encoding the human ⁇ domain and a nucleic acid sequence encoding the cognate human VH domain; and, (e) using the cloned nucleic acid sequence encoding the human ⁇ /k domain and the cloned nucleic acid sequence encoding the cognate human V H domain to make a fully human antibody.
  • a method for making a rearranged antibody light chain variable region gene sequence comprising (a) exposing a mouse as described in this disclosure to an antigen; (b) allowing the mouse to mount an immune response; (c) identifying a cell in the mouse that comprises a nucleic acid sequence that encodes a rearranged human ⁇ / ⁇ domain sequence contiguous on the same nucleic acid molecule with a nucleic acid sequence encoding a mouse CK domain, wherein the cell also encodes a cognate heavy chain comprising a human V H domain and a mouse CH domain, and wherein the cell expresses an antibody that binds the antigen; (d) cloning from the cell a nucleic acids sequence encoding the human ⁇ / ⁇ domain and a nucleic acid sequence encoding the cognate human V H domain; and, (e) using the cloned nucleic acid sequence encoding the human VX domain and the cloned nucleic
  • a method for making a rearranged antibody light chain variable region gene sequence comprising (a) exposing a mouse as described herein to an antigen; (b) allowing the mouse to mount an immune response to the antigen; (c) identifying a cell in the mouse that comprises DNA that encodes a rearranged human ⁇ / ⁇ domain sequence fused with a mouse CX domain, wherein the cell also encodes a cognate heavy chain comprising a human V H domain and a mouse CH domain, and wherein the cell expresses an antibody that binds the antigen; (d) cloning from the cell a nucleic acid sequence encoding the rearranged human VX domain and a nucleic acid sequence encoding the cognate human V H domain; and, (e) using the cloned nucleic acid sequence encoding the human VX domain and the cloned nucleic acid sequence encoding the cognate human VH domain to make a fully human antibody.
  • the mouse CX domain is mouse CX2.
  • the mouse CX domain is derived from a CX gene that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse CX2.
  • a genetically modified mouse that expresses a human ⁇ -derived light chain fused to an endogenous light chain constant region (C L ), wherein the mouse, upon immunization with antigen, makes an antibody comprising a human VX domain fused to a mouse C L domain.
  • the mouse C L domain is selected from a CK domain and a CX domain.
  • the mouse C L domain is a CK domain.
  • the mouse C L domain is a CX domain.
  • the CX domain is CX2.
  • the mouse CX domain is derived from a CX gene that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse CX2.
  • a genetically modified mouse comprising a modified endogenous K or X light chain locus as described herein, is provided that expresses a plurality of immunoglobulin X light chains associated with a plurality of immunoglobulin heavy chains.
  • the heavy chain comprises a human sequence.
  • the human sequence is selected from a variable sequence, a C H 1 , a hinge, a C H 2, a C H 3, and a combination thereof.
  • immunoglobulin X light chains comprises a human sequence.
  • the human sequence is selected from a variable sequence, a constant sequence, and a combination thereof.
  • the mouse comprises a disabled endogenous immunoglobulin locus and expresses the heavy chain and/or the X light chain from a transgene or extrachromosomal episome.
  • the mouse comprises a replacement at an endogenous mouse locus of some or all endogenous mouse heavy chain gene segments (i.e., V, D, J), and/or some or all endogenous mouse heavy chain constant sequences (e.g., C H 1 , hinge, CH2, C H 3, or a combination thereof), and/or some or all endogenous mouse light chain sequences (e.g., V, J, constant, or a combination thereof), with one or more human immunoglobulin sequences.
  • endogenous mouse heavy chain gene segments i.e., V, D, J
  • endogenous mouse heavy chain constant sequences e.g., C H 1 , hinge, CH2, C H 3, or a combination thereof
  • endogenous mouse light chain sequences e.g., V, J, constant, or a combination thereof
  • a mouse suitable for making antibodies that have a human ⁇ - derived light chain wherein all or substantially all antibodies made in the mouse are expressed with a human ⁇ -derived light chain.
  • the human ⁇ -derived light chain is expressed from an endogenous light chain locus.
  • the endogenous light chain locus is a ⁇ light chain locus.
  • the ⁇ light chain locus is a mouse ⁇ light chain locus.
  • a method for making a ⁇ -derived light chain for a human antibody comprising obtaining from a mouse as described herein a light chain sequence and a heavy chain sequence, and employing the light chain sequence and the heavy chain sequence in making a human antibody.
  • a method for making an antigen-binding protein comprising exposing a mouse as described herein to an antigen; allowing the mouse to mount an immune response; and obtaining from the mouse an antigen-binding protein that binds the antigen, or obtaining from the mouse a sequence to be employed in making an antigen-binding protein that binds the antigen.
  • a cell derived from a mouse as described herein is provided.
  • the cell is selected from an embryonic stem cell, a pluripotent cell, an induced pluripotent cell, a B cell, and a hybridoma.
  • a cell that comprises a genetic modification as described herein.
  • the cell is a mouse cell.
  • the cell is selected from a hybridoma and a quadroma.
  • the cell expresses an immunoglobulin light chain that comprises a human ⁇ variable sequence fused with a mouse constant sequence.
  • the mouse constant sequence is a mouse K constant sequence.
  • tissue derived from a mouse as described herein is provided.
  • the antigen-binding protein is a human protein.
  • the human protein is a human antibody.
  • an antigen-binding protein made by a mouse, cell, tissue, or method as described herein is provided.
  • the antigen-binding protein is a human protein.
  • the human protein is a human antibody.
  • FIG. 1 shows a detailed illustration, not to scale, of the human ⁇ light chain locus including the clusters of ⁇ ⁇ gene segments (A, B and C) and the ⁇ and C region pairs (J-C pairs)
  • FIG. 2 shows a general illustration, not to scale, of a targeting strategy used to inactivate the endogenous mouse ⁇ light chain locus.
  • FIG. 3 shows a general illustration, not to scale, of a targeting strategy used to inactivate the endogenous mouse ⁇ light chain locus.
  • FIG. 4A shows a general illustration, not to scale of an initial targeting vector for targeting the endogenous mouse ⁇ light chain locus with human ⁇ light chain sequences including 12 hV gene segments and hJX1 gene segment (12/1- ⁇ Targeting Vector).
  • FIG. 4B shows a general illustration, not to scale, of four initial targeting vectors for targeting the endogenous mouse ⁇ light chain locus with human ⁇ light chain sequences including 12 hN ⁇ gene segments and hJ 1 gene segment (12/1- ⁇ Targeting Vector), 12 hA/ ⁇ gene segments and hJ 1 , 2, 3 and 7 gene segments (12/4- ⁇ Targeting Vector), 12 hV gene segments, a human V -JK genomic sequence and ⁇ 1 gene segment (12( ⁇ )1- ⁇ Targeting Vector) and 12 hV gene segments, a human VK-JK genomic sequence and hJ 1 , 2, 3 and 7 gene segments (12( ⁇ )4- ⁇ Targeting Vector).
  • FIG. 5A shows a general illustration, not to scale, of a targeting strategy for progressive insertion of 40 hVX gene segments and a single J gene segment into the mouse ⁇ light chain locus.
  • FIG. 5B shows a general illustration, not to scale, of a targeting strategy for progressive insertion of 40 hVX gene segments and a single hJ gene segment into the mouse K locus.
  • FIG. 6 show a general illustration, not to scale, of the targeting and molecular engineering steps employed to make unique human ⁇ - ⁇ hybrid targeting vectors for construction of a hybrid light chain locus containing a human ⁇ intergenic sequence, multiple J gene segments or both.
  • FIG. 7A shows a general illustration, not to scale, of the locus structure for a modified mouse ⁇ light chain locus containing 40 hV gene segments and a single bJk gene segment operably linked to the endogenous Ck2 gene.
  • FIG. 7B shows a general illustration, not to scale, of the locus structure for four independent, modified mouse ⁇ light chain loci containing 40 hN ⁇ gene segments and either one or four bJk gene segments with or without a contiguous human VK-JK genomic sequence operably linked to the endogenous CK gene.
  • FIG. 8A shows contour plots of lg + and lgK + splenocytes gated on CD19 + from a wild type mouse (WT), a mouse homozygous for 12 hV and four bJk gene segments including a human VK-JK genomic sequence (12hV -VKjK-4hJ ) and a mouse
  • FIG. 8B shows the total number of CD19 + B cells in harvested spleens from wild type (WT), mice homozygous for 12 hV and four bJk gene segments including a human VK-JK genomic sequence (12hV -VKjK-4hJ ) and mice homozygous for 40 hV and one bJk gene segment (40hVX-1 hJ ).
  • FIG. 9A in the top panel, shows contour plots of splenocytes gated on singlets and stained for B and T cells (CD19 + and CD3 + , respectively) from a wild type mouse (WT) and a mouse homozygous for 40 hV and four Jk gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJ ).
  • the bottom panel shows contour plots of splenocytes gated on CD19 + and stained for ⁇ gk + and lgK + expression from a wild type mouse (WT) and a mouse homozygous for 40 hV and four Jk gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJ ).
  • FIG. 9B shows the total number of CD19 + , CD19 + !g K + and CD19 + lg + B cells in harvested spleens from wild type mice (WT) and mice homozygous for 40 bVk and four Jk gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJ ).
  • FIG. 9C shows contour plots of splenocytes gated on CD19 + and stained for immunoglobulin D (IgD) and immunoglobulin M (IgM) from a wild type mouse (WT) and a mouse homozygous for 40 hVX and four JX gene segments including a human VK-JK genomic sequence (40hVX-VKjK-4hJ ).
  • Mature (72 for WT, 51 for 40hV -VKjK-4h ⁇ ) and transitional (13 for WT, 22 for 40hVX-VKjK-4hJ ) B cells are noted on each of the contour plots.
  • FIG. 9D shows the total number of CD19 + B cells, transitional B cells
  • FIG. 10A shows contour plots of bone marrow stained for B and T cells (CD19 + and CD3 + , respectively) from a wild type mouse (WT) and a mouse homozygous for 40 hN ⁇ and four ⁇ gene segments including a human VK-JK genomic sequence (401 ⁇ - ⁇ -4 ⁇ ).
  • the bottom panel shows contour plots of bone marrow gated on CD19 + and stained for ckit + and CD43 + from a wild type mouse (WT) and a mouse homozygous for 40 hN ⁇ and four ⁇ gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJ ). Pro and Pre B cells are noted on the contour plots of the bottom panel.
  • FIG. 10B shows the number of Pro (CD19 + CD43 + ckit + ) and Pre (CD19 + CD43 ⁇ ckir) B cells in bone marrow harvested from the femurs of wild type mice (WT) and mice homozygous for 40 hN ⁇ and four ⁇ gene segments including a human VK-JK genomic sequence (40 A -VKjK-4hJX).
  • FIG. 10C shows contour plots of bone marrow gated on singlets stained for immunoglobulin M (IgM) and B220 from a wild type mouse (WT) and a mouse
  • FIG. 10D shows the total number of immature (B220 int lgM + ) and mature (B220 hl lgM + ) B cells in bone marrow isolated from the femurs of wild type mice (WT) and mice homozygous for 40 ⁇ and four J gene segments including a human VK-JK genomic sequence
  • FIG. 10E shows contour plots of bone marrow gated on immature (B220 int lgM + ) and mature (B220 h, lgM + ) B cells stained for and IgK expression isolated from the femurs of a wild type mouse (WT) and a mouse homozygous for 40 hV and four J ⁇ gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJX).
  • FIG. 1 1 shows a nucleotide sequence alignment of the V -J -CK junction of eighteen independent RT-PCR clones amplified from splenocyte RNA of mice bearing human ⁇ light chain gene sequences at an endogenous mouse ⁇ light chain locus.
  • FIG. 12 shows a nucleotide sequence alignment of the ⁇ / ⁇ - ⁇ - ⁇ junction of twelve independent RT-PCR clones amplified from splenocyte RNA of mice bearing human ⁇ light chain gene sequences including a contiguous human VK-JK genomic sequence at an endogenous mouse ⁇ light chain locus.
  • FIG. 13 shows a nucleotide sequence alignment of the ⁇ ⁇ - ⁇ - ⁇ junction of three independent RT-PCR clones amplified from splenocyte RNA of mice bearing human ⁇ light chain gene sequences at an endogenous mouse ⁇ light chain locus.
  • 2D1 SEQ ID NO:101 ;
  • 2D9 SEQ ID NO:102;
  • 3E15 SEQ ID NO:103.
  • Lower case bases indicate non-germline bases resulting from either mutation and/or N addition during recombination.
  • Consensus amino acids within the Framework 4 region (FWR4) encoded by the nucleotide sequence of hJ 1 and mouse C 2 are noted at the bottom of the sequence alignment.
  • a contiguous sequence includes reference to occurrence on the same nucleic acid molecule, e.g., two nucleic acid sequences are “contiguous” if they occur on the same nucleic molecule but are interrupted by another nucleic acid sequence.
  • a rearranged V(D)J sequence is "contiguous” with a constant region gene sequence, although the final codon of the V(D)J sequence is not followed immediately by the first codon of the constant region sequence.
  • two V gene segment sequences are "contiguous” if they occur on the same genomic fragment, although they may be separated by sequence that does not encode a codon of the V region, e.g. , they may be separated by a regulatory sequence, e.g., a promoter or other noncoding sequence.
  • a contiguous sequence includes a genomic fragment that contains genomic sequences arranged as found in a wild-type genome.
  • variable region when used concerning a variable region "derived from” a cited gene or gene segment includes the ability to trace the sequence back to a particular unrearranged gene segment or gene segments that were rearranged to form a gene that expresses the variable domain (accounting for, where applicable, splice differences and somatic mutations).
  • variable region gene segment or joining gene segment refers to usage in an expressed antibody repertoire; e.g. , in humans ⁇ gene segments 3-1 , 4-3, 2-8, etc. are functional, whereas ⁇ gene segments 3-2, 3-4, 2-5, etc. are nonfunctional.
  • a "heavy chain locus” includes a location on a chromosome, e.g., a mouse chromosome, wherein in a wild-type mouse heavy chain variable (V H ) , heavy chain diversity (D H ), heavy chain joining (J H ), and heavy chain constant (C H ) region DNA sequences are found.
  • V H mouse heavy chain variable
  • D H heavy chain diversity
  • J H heavy chain joining
  • C H heavy chain constant
  • a "K locus” includes a location on a chromosome, e.g., a mouse chromosome, wherein in a wild-type mouse Kvariable (VK), K joining (JK), and ⁇ constant (CK) region DNA sequences are found.
  • VK wild-type mouse Kvariable
  • JK K joining
  • CK ⁇ constant
  • a " ⁇ locus” includes a location on a chromosome, e.g., a mouse chromosome, wherein in a wild-type mouse ⁇ variable (VX), ⁇ joining ( ⁇ ), and ⁇ constant (C ) region DNA sequences are found.
  • VX mouse ⁇ variable
  • ⁇ joining
  • C ⁇ constant
  • the term "unrearranged” includes the state of an immunoglobulin locus wherein V gene segments and J gene segments (for heavy chains, D gene segments as well) are maintained separately but are capable of being joined to form a rearranged V(D)J gene that comprises a single V,(D),J of the V(D)J repertoire.
  • mice that express antibodies that are fully human, or partly human and partly mouse have previously been reported.
  • VELOCIMMUNE® genetically engineered mice comprise a replacement of unrearranged V(D)J gene segments at endogenous mouse loci with human V(D)J gene segments.
  • VELOCIMMUNE® mice express chimeric antibodies having human variable domains and mouse constant domains (see, e.g., US Pat. No. 7,605,237).
  • Antibody light chains are encoded by one of two separate loci: kappa ( ⁇ ) and lambda ( ⁇ ).
  • Mouse antibody light chains are primarily of the ⁇ type. Mice that make mouse antibodies, and modified mice that make fully human or chimeric human-mouse antibodies, display a bias in light chain usage. Humans also exhibit light chain bias, but not so pronounced as in mice; the ratio of ⁇ light chains to ⁇ light chains in mice is about 95:5, whereas in humans the ratio is about 60:40. The more pronounced bias in mice is not thought to severely affect antibody diversity, because in mice the ⁇ variable locus is not so diverse in the first instance. This is not so in humans. The human ⁇ light chain locus is richly diverse.
  • the human ⁇ light chain locus extends over 1 ,000 kb and contains over 80 genes that encode variable (V) or joining (J) segments (FIG. 1 ). Within the human ⁇ light chain locus, over half of all observed ⁇ domains are encoded by the gene segments 1 -40, 1 -44, 2-8, 2-14, and 3-21 . Overall, about 30 or so of the human ⁇ / ⁇ gene segments are believed to be functional. There are seven ⁇ gene segments, only four of which are regarded as generally functional ⁇ gene segments— ⁇ 1 , ⁇ 2, ⁇ 3, and ⁇ 7.
  • the ⁇ light chain locus in humans is similar in structure to the ⁇ locus of both mice and humans in that the human ⁇ light chain locus has several variable region gene segments that are capable of recombining to form a functional light chain protein.
  • the human ⁇ light chain locus contains approximately 70 V gene segments and 7 ⁇ - ⁇ gene segment pairs. Only four of these ⁇ - ⁇ gene segment pairs appear to be functional. In some alleles, a fifth ⁇ - ⁇ gene segment pair is reportedly a pseudo gene ( ⁇ 6).
  • the 70 ⁇ / ⁇ gene segments appear to contain 38 functional gene segments.
  • the 70 ⁇ / ⁇ sequences are arranged in three clusters, all of which contain different members of distinct V gene family groups (clusters A, B and C; FIG. 1 ). This is a potentially rich source of relatively untapped diversity for generating antibodies with human V regions in non-human animals.
  • mice ⁇ light chain locus contains only two or three (depending on the strain) mouse V region gene segments (FIG. 2). At least for this reason, the severe ⁇ bias in mice is not thought to be particularly detrimental to total antibody diversity.
  • the locus consists essentially of two clusters of gene segments within a span of approximately 200 kb (FIG.2).
  • the two clusters contain two sets of V, J, and C genes that are capable of independent rearrangement: ⁇ / ⁇ 2- ⁇ 2- ⁇ 2- ⁇ 4- ⁇ 4 and ⁇ 1 - ⁇ 3- ⁇ 3- ⁇ 1 - ⁇ 1 .
  • V 2 has been found to recombine with all ⁇ gene segments, ⁇ 1 appears to exclusively recombine with C 1 .
  • CX4 is believed to be a pseudo gene with defective splice sites.
  • mouse ⁇ light chain locus is strikingly different.
  • the structure and number of gene segments that participate in the recombination events leading to a functional light chain protein from the mouse ⁇ locus is much more complex (FIG. 3).
  • mouse ⁇ light chains do not greatly contribute to the diversity of an antibody population in a typical mouse.
  • Exploiting the rich diversity of the human ⁇ light chain locus in mice would likely result in, among other things, a source for a more complete human repertoire of light chain V domains. Previous attempts to tap this diversity used human transgenes containing chunks of the human ⁇ light chain locus randomly incorporated into the mouse genome (see, e.g., US 6,998,514 and US 7,435,871 ).
  • mice containing these randomly integrated transgenes reportedly express fully human ⁇ light chains, however, in some cases, one or both endogenous light chain loci remain intact. This situation is not desirable as the human ⁇ light chain sequences contend with the mouse light chain ( ⁇ or ⁇ ) in the expressed antibody repertoire of the mouse.
  • mice that are capable of expressing one or more ⁇ light chain nucleic acid sequences directly from a mouse light chain locus, including by replacement at an endogenous mouse light chain locus.
  • mice capable of expressing human ⁇ light chain sequences from an endogenous locus may be further bred to mice that comprise a human heavy chain locus and thus be used to express antibodies comprising V regions (heavy and light) that are fully human.
  • the V regions express with mouse constant regions.
  • no endogenous mouse immunoglobulin gene segments are present and the V regions express with human constant regions.
  • mice Many advantages can be realized for various embodiments of expressing binding proteins derived from human ⁇ /k and ⁇ gene segments in mice. Advantages can be realized by placing human ⁇ sequences at an endogenous light chain locus, for example, the mouse ⁇ or ⁇ locus. Antibodies made from such mice can have light chains that comprise human Vk domains fused to a mouse C L region, specifically a mouse CK or Ck region. The mice will also express human ⁇ / ⁇ domains that are suitable for
  • mice that comprise an unrearranged ⁇ / ⁇ gene segment at an immunoglobulin ⁇ or ⁇ light chain locus.
  • Mice that express antibodies that comprise a light chain having a human ⁇ / ⁇ domain fused to a CK and/or Ck region are described.
  • the genetically modified mice comprise certain non-coding sequence(s) from a human locus.
  • the genetically modified mouse comprises human ⁇ and ⁇ gene segments at an endogenous ⁇ light chain locus, and further comprises a human ⁇ light chain genomic fragment.
  • the human ⁇ light chain genomic fragment is a non-coding sequence naturally found between a human VK gene segment and a human JK gene segment.
  • the human and mouse ⁇ light chain loci contain sequences that encode sterile transcripts that lack either a start codon or an open reading frame, and that are regarded as elements that regulate transcription of the ⁇ light chain loci. These sterile transcripts arise from an intergenic sequence located downstream or 3' of the most proximal VK gene segment and upstream or 5' of the ⁇ light chain intronic enhancer ( ⁇ ) that is upstream of the K light chain constant region gene (CK). The sterile transcripts arise from
  • a replacement of the ⁇ light chain locus upstream of the CK gene would remove the intergenic region encoding the sterile transcripts. Therefore, in various embodiments, a replacement of mouse ⁇ light chain sequence upstream of the mouse CK gene with human ⁇ light chain gene segments would result in a humanized mouse ⁇ light chain locus that contains human ⁇ and ⁇ gene segments but not the ⁇ light chain intergenic region that encodes the sterile transcripts.
  • This observation is consistent with a hypothesis that the intergenic region— directly through a sterile transcript, or indirectly— suppresses usage from the endogenous ⁇ light chain locus. Under such a hypothesis, including the intergenic region would result in a decrease in usage of the endogenous ⁇ light chain locus, leaving the mouse a restricted choice but to employ the modified ( ⁇ into ⁇ ) locus to generate antibodies.
  • a replacement of mouse ⁇ light chain sequence upstream of the mouse CK gene with human ⁇ light chain sequence further comprises a human ⁇ light chain intergenic region disposed, with respect to transcription, between the 3' untranslated region of the 3' most ⁇ / ⁇ gene segment and 5' to the first human JX gene segment.
  • a human ⁇ light chain intergenic region may be omitted from a replaced endogenous ⁇ light chain locus (upstream of the mouse CK gene) by making a deletion in the endogenous ⁇ light chain locus.
  • the mouse generates antibodies from an endogenous ⁇ light chain locus containing human ⁇ light chain sequences.
  • mice that make antibodies that contain a light chain that has a human ⁇ / ⁇ domain fused to an endogenous C L (e.g. CK or CX) region are described. Genetic modifications are described that, in various embodiments, comprise a deletion of one or both endogenous light chain loci. For example, to eliminate mouse ⁇ light chains from the endogenous antibody repertoire a deletion of a first VX-JX-CX gene cluster and replacement, in whole or in part, of the VX-JX gene segments of a second gene cluster with human VX-JX gene segments can be made. Genetically modified mouse embryos, cells, and targeting constructs for making the mice, mouse embryos, and cells are also provided.
  • endogenous C L e.g. CK or CX
  • the modification does not affect the assembly of a functional membrane-bound antibody molecule involving an endogenous heavy chain and a light chain, e.g., a hVX domain linked to a mouse CX region.
  • a functional membrane-bound antibody molecule involving an endogenous heavy chain and a light chain, e.g., a hVX domain linked to a mouse CX region.
  • animals containing a replacement of the ⁇ ⁇ - ⁇ gene segments of an endogenous ⁇ / ⁇ - ⁇ - CX gene cluster with human ⁇ ⁇ - ⁇ gene segments should be able to make normal ⁇ light chains that are capable of binding antigen during an immune response through the human ⁇ / ⁇ - ⁇ gene segments present in the expressed antibody repertoire of the animal.
  • FIG. 2 A schematic illustration (not to scale) of a deleted endogenous mouse ⁇ / ⁇ - ⁇ - ⁇ gene cluster is provided in FIG. 2. As illustrated, the mouse ⁇ light chain locus is organized into two gene clusters, both of which contain function gene segments capable of recombining to form a function mouse ⁇ light chain.
  • the endogenous mouse ⁇ 1- ⁇ 3- ⁇ 3- J 1 -C 1 gene cluster is deleted by a targeting construct (Targeting Vector 1 ) with a neomycin cassette flanked by recombination sites.
  • the other endogenous gene cluster (V 2-VX3-J 2-C 2-JX4-C 4) is deleted in part by a targeting construct (Targeting Vector 2) with a hygromycin-thymidine kinase cassette flanked by recombination sites.
  • a targeting construct (Targeting Vector 2) with a hygromycin-thymidine kinase cassette flanked by recombination sites.
  • the second targeting construct (Targeting Vector 2) is constructed using recombination sites that are different than those in the first targeting construct (Targeting Vector 1 ) thereby allowing for the selective deletion of the selection cassette after a successful targeting has been achieved.
  • the resulting double-targeted locus is functionally silenced in that no endogenous ⁇ light chain can be produced.
  • This modified locus can be used for the insertion of human ⁇ and ⁇ gene segments to create an endogenous mouse ⁇ locus comprising human VX and ⁇ gene segments, whereby, upon recombination at the modified locus, the animal produces ⁇ light chains comprising rearranged human V and ⁇ gene segments linked to an endogenous mouse CX gene segment.
  • a genetically modified mouse that expresses a hVX linked to a mouse CX gene having been recombined at the endogenous mouse ⁇ light chain locus can be made by any method known in the art.
  • a schematic illustration (not to scale) of the replacement of the endogenous mouse ⁇ 2 ⁇ ⁇ 3- ⁇ 2 gene segments with human V and ⁇ gene segments is provided in FIG. 4A.
  • an endogenous mouse ⁇ light chain locus that had been rendered nonfunctional is replaced by a targeting construct (12/1- ⁇ Targeting Vector) that includes a neomycin cassette flanked by recombination sites.
  • the ⁇ 2 ⁇ ⁇ 3- ⁇ 2 gene segments are replaced with a genomic fragment containing human ⁇ sequence that includes 12 hN/ ⁇ gene segments and a single hJk gene segment.
  • this first approach positions one or more hN ⁇ gene segments at the endogenous ⁇ light chain locus contiguous with a single ⁇ gene segment (FIG. 4A).
  • FIG. 5A schematic illustrations of two additional targeting constructs (+16- ⁇ and +12- ⁇ Targeting Vectors) used for progressive insertion of addition human hV gene segments are provided in FIG. 5A.
  • additional genomic fragments containing specific human hN/ ⁇ gene segments are inserted into the modified endogenous ⁇ light chain locus in successive steps using homology provided by the previous insertion of human ⁇ light chain sequences.
  • 28 additional hX ⁇ gene segments are inserted into the modified endogenous ⁇ light chain locus. This creates a chimeric locus that produces a ⁇ light chain protein that comprises human ⁇ / ⁇ - ⁇ gene segments linked to a mouse ⁇ gene.
  • compositions and methods for making a mouse that expresses a light chain comprising hN/ ⁇ and ⁇ gene segments operably linked to a mouse CX gene segment are provided, including compositions and method for making a mouse that expresses such genes from an endogenous mouse ⁇ light chain locus.
  • the methods include selectively rendering one endogenous mouse ⁇ / ⁇ - ⁇ - ⁇ gene cluster nonfunctional (e.g., by a targeted deletion), and employing a hX ⁇ and ⁇ gene segments at the endogenous mouse ⁇ light chain locus to express a hX ⁇ domain in a mouse.
  • human ⁇ light chain gene segments may be positioned at the endogenous ⁇ light chain locus.
  • the genetic modification comprises a deletion of the endogenous ⁇ light chain locus.
  • a deletion of the mouse VK and JK gene segments can be made.
  • Genetically modified mouse embryos, cells, and targeting constructs for making the mice, mouse embryos, and cells are also provided.
  • FIG. 3 A schematic illustration (not to scale) of deleted mouse VK and JK gene segments is provided in FIG. 3.
  • the endogenous mouse VK and JK gene segments are deleted via recombinase-mediated deletion of mouse sequences position between two precisely positioned targeting vectors each employing site-specific recombination sites.
  • a first targeting vector JK Targeting Vector
  • a second targeting vector VK Targeting Vector
  • VK Targeting Vector is employed in a second, sequential targeting event to delete a sequence located 5' of the most distal mouse VK gene segment.
  • Both targeting vectors contain site-specific recombination sites thereby allowing for the selective deletion of both selection cassettes and all intervening mouse ⁇ light chain sequences after a successful targeting has been achieved.
  • the resulting deleted locus is functionally silenced in that no endogenous ⁇ light chain can be produced.
  • This modified locus can be used for the insertion of ⁇ and J gene segments to create an endogenous mouse ⁇ locus comprising hV and J gene segments, whereby, upon recombination at the modified locus, the animal produces ⁇ light chains comprising rearranged hV and J gene segments operably linked to an endogenous mouse CK gene segment.
  • Various targeting vectors comprising human ⁇ light chain sequences can be used in conjunction with this deleted mouse ⁇ locus to create a hybrid light chain locus containing human ⁇ gene segments operably linked with a mouse CK region.
  • a second approach positions one or more human ⁇ gene segments are positioned at the mouse ⁇ light chain locus contiguous with a single human J gene segment (12/1 - ⁇ Targeting Vector, FIG. 4B).
  • modifications to this approach can be made to add gene segments and/or regulatory sequences to optimize the usage of the human ⁇ light chain sequences from the mouse ⁇ locus within the mouse antibody repertoire.
  • one or more hV gene segments are positioned at the mouse K light chain locus contiguous with four hJ gene sequences (12/4- ⁇ Targeting Vector FIG. 4B).
  • one or more ⁇ / ⁇ gene segments are positioned at the mouse K light chain locus contiguous with a human ⁇ intergenic sequence and a single hJ gene sequence (12( ⁇ )1 - ⁇ Targeting Vector, FIG. 4B).
  • one or more hV gene segments are positioned at the mouse K light chain locus contiguous with a human ⁇ intergenic sequence four ⁇ gene sequences (12( ⁇ )4- ⁇ Targeting Vector FIG. 4B).
  • genetically modified mouse comprise a knockout of the endogenous mouse ⁇ light chain locus.
  • the ⁇ light chain locus is knocked out by a strategy that deletes the region spanning ⁇ / ⁇ 2 to ⁇ 2, and the region spanning ⁇ 1 to C ⁇ (FIG. 2). Any strategy that reduces or eliminates the ability of the endogenous ⁇ light chain locus to express endogenous ⁇ domains is suitable for use with embodiments in this disclosure.
  • mice comprising human ⁇ sequences at either the mouse ⁇ or ⁇ light chain locus will express a light chain that comprises a V region fused to a mouse C L (CK or CX) region.
  • a functionally silenced light chain locus e.g., a knockout of the endogenous mouse ⁇ or ⁇ light chain locus
  • (b) comprise an endogenous mouse ⁇ light chain locus that comprises hV and hJ gene segments operably linked to an endogenous mouse C gene
  • (c) comprise an endogenous mouse ⁇ light chain locus that comprises h and hJK gene segments operably linked to an endogenous mouse CK gene
  • the antibodies that comprise the hV domains expressed in the context of either CK or ⁇ are used to make fully human antibodies by cloning the nucleic acids encoding the hX ⁇ domains into expression constructs that bear genes encoding human C . Resulting expression constructs are transfected into suitable host cells for expressing antibodies that display a fully hVX domain fused to hC .
  • Various targeting constructs were made using VELOCIGENE® technology (see, e.g., US Pat. No. 6,586,251 and Valenzuela et al. (2003) High-throughput engineering of the mouse genome coupled with high-resolution expression analysis, Nature Biotech. 21 (6):652-659) to modify mouse genomic Bacterial Artificial Chromosome (BAC) libraries to inactivate the mouse ⁇ and ⁇ light chain loci.
  • BAC Bacterial Artificial Chromosome
  • proximal cluster comprising VX1-J 3-C 3-J 1-C 1 gene segments was deleted in a single targeting event using a targeting vector comprising a neomycin cassette flanked by loxP sites with a 5' mouse homology arm containing sequence 5' of the ⁇ 1 gene segment and a 3' mouse homology arm containing sequence 3' of the C 1 gene segment (FIG. 2, Targeting Vector 1).
  • a second targeting construct was prepared to precisely delete the distal endogenous mouse ⁇ gene cluster containing ⁇ 2- ⁇ 2- ⁇ 2- ⁇ 4- ⁇ 4 except that the targeting construct contained a 5' mouse homology arm that contained sequence 5' of the ⁇ 2 gene segment and a 3' mouse homology arm that contained sequence 5' to the endogenous C 2 gene segment (FIG. 2, Targeting Vector 2).
  • the second targeting construct precisely deleted V 2-JX2, while leaving C 2-JX4-C 4 intact at the endogenous mouse ⁇ locus.
  • ES cells containing an inactivated endogenous ⁇ locus were confirmed by karyotyping and screening methods (e.g., TAQMAN®) known in the art.
  • DNA was then isolated from the modified ES cells and subjected to treatment with CRE recombinase thereby mediating the deletion of the proximal targeting cassette containing the neomycin marker gene, leaving only a single loxP site at the deletion point (FIG. 2, bottom).
  • the JK gene segments (1-5) of the endogenous mouse ⁇ light chain locus were deleted in a single targeting event using a targeting vector comprising a hygromycin-thymidine kinase (hyg-TK) cassette containing a single loxP site 3' to the hyg- T cassette (FIG. 3, JK Targeting Vector).
  • the homology arms used to make this targeting vector contained mouse genomic sequence 5' and 3' of the endogenous mouse JK gene segments.
  • a second targeting vector was prepared to delete a portion of mouse genomic sequence upstream (5') to the most distal endogenous mouse VK gene segment (FIG. 3, VK Targeting Vector).
  • This targeting vector contained an inverted /ox51 1 site, a loxP site and a neomycin cassette.
  • the homology arms used to make this targeting vector contained mouse genomic sequence upstream of the most distal mouse VK gene segment.
  • the targeting vectors were used in a sequential fashion (i.e., JK then VK) to target DNA in ES cells.
  • ES bearing a double-targeted chromosome i.e., a single endogenous mouse ⁇ locus targeted with both targeting vectors
  • were confirmed by karyotyping and screening methods e.g., TaqmanTM
  • DNA was then isolated from the modified ES cells and subjected to treatment with Cre recombinase thereby mediating the deletion of endogenous mouse VK gene segments and both selection cassettes, while leaving two juxtaposed lox sites in opposite orientation relative to one another (FIG. 3, bottom; SEQ ID NO:1 ).
  • FIGs. 4A and 4B show the targeting vectors that were constructed for making an initial insertion of human ⁇ light chain gene segments at the mouse ⁇ and ⁇ light chain loci, respectively.
  • a 124,125 bp DNA fragment from the 729g4 BAC clone containing 12 hV gene segments and a hJ 1 gene segment was engineered to contain a Pl-Scel site 996 bp downstream (3') of the hJX1 gene segment for ligation of a 3' mouse homology arm.
  • Two different sets of homology arms were used for ligation to this human fragment; one set of homology arms contained endogenous mouse ⁇ sequences from the 135k15 BAC clone (FIG.4A) and another set contained endogenous ⁇ sequence 5' and 3' of the mouse VK and J gene segments from mouse BAC clones RP23-302g12 and RP23-254m04, respectively (FIG. 4B).
  • the ⁇ 28 kb mouse fragment was used as a 3' homology arm by ligation to the ⁇ 124 kb human ⁇ fragment, which created a 3' junction containing, from 5' to 3', a ⁇ gene segment, 996 bp of human ⁇ sequence 3' of the hJ 1 gene segment, 1229 bp of mouse ⁇ sequence 5' to the mouse 0X2 gene, the mouse C 2 gene and the remaining portion of the ⁇ 28 kb mouse fragment.
  • Upstream (5') from the human V 3-12 gene segment was an additional 1456 bp of human ⁇ sequence before the start of the 5' mouse homology arm, which contained 23,792 bp of mouse genomic DNA corresponding to sequence 5' of the endogenous mouse ⁇ locus. Between the 5' homology arm and the beginning of the human ⁇ sequence was a neomycin cassette flanked by Frt sites.
  • the 12/1- ⁇ Targeting Vector included, from 5' to 3', a 5' homology arm containing ⁇ 24 kb of mouse ⁇ genomic sequence 5' of the endogenous ⁇ locus, a 5' Frt site, a neomycin cassette, a 3' Frt site, ⁇ 123 kb of human genomic ⁇ sequence containing the first 2 consecutive hV gene segments and a ⁇ gene segment, a Pl-Scel site, and a 3' homology arm containing ⁇ 28 kb of mouse genomic sequence including the endogenous ⁇ 2- ⁇ 4- ⁇ 4 gene segments, the mouse enhancer 2.4 sequence and additional mouse genomic sequence downstream (3') of the enhancer 2.4 (FIG. 4A).
  • the 12/1- ⁇ Targeting Vector (FIG. 4B) employed the same ⁇ 124 human ⁇ fragment with the exception that mouse homology arms containing mouse ⁇ sequence were used such that targeting to the endogenous ⁇ locus could be achieved by homologous recombination.
  • the 12/1 - ⁇ Targeting Vector included, from 5' to 3', a 5' homology arm containing ⁇ 23 kb of mouse genomic sequence 5' of the endogenous ⁇ locus, an l-Ceul site, a 5' Frt site, a neomycin cassette, a 3' Frt site, ⁇ 124 kb of human genomic ⁇ sequence containing the first 12 consecutive ⁇ gene segments and a hJ 1 gene segment, a Pl-Scel site, and a 3' homology arm containing ⁇ 28 kb of mouse genomic sequence including the endogenous the mouse CK gene, ⁇ and ⁇ 3' and additional mouse genomic sequence downstream (3') of ⁇ 3' (FIG. 4B, 12/1- ⁇ Targeting Vector).
  • a human ⁇ mini-locus with 12 human V and four human ⁇ gene segments In another approach to add diversity to a chimeric ⁇ light chain locus, a third initial targeting vector was engineered to insert the first 12 consecutive human V gene segments from cluster A and hJ 1 , 2, 3 and 7 gene segments into the mouse ⁇ light chain locus (FIG. 4B, 12/4- ⁇ Targeting Vector).
  • a DNA segment containing hJ 1 , JX2, ⁇ 3 and ⁇ 7 gene segments was made by de novo DNA synthesis (Integrated DNA Technologies) including each ⁇ gene segment and human genomic sequence of ⁇ 100 bp from both the immediate 5' and 3' regions of each ⁇ gene segment.
  • a Pl-Scel site was engineered into the 3' end of this ⁇ 1 kb DNA fragment and ligated to a chloroamphenicol cassette.
  • Homology arms were PCR amplified from human ⁇ sequence at 5' and 3' positions relative to the bJX1 gene segment of the human BAC clone 729g4. Homologous recombination with this intermediate targeting vector was performed on a modified 729g4 BAC clone that had been previously targeted upstream (5') of the human ⁇ 3-12 gene segment with a neomycin cassette flanked by Frt sites, which also contained an l-Ceul site 5' to the 5' Frt site.
  • the double-targeted 729g4 BAC clone included from 5' to 3' an l-Ceul site, a 5' Frt site, a neomycin cassette, a 3' Frt site, a ⁇ 123 kb fragment containing the first 12 hV gene segments, a ⁇ 1 kb fragment containing human ⁇ 1 , 2, 3 and 7 gene segments, a Pl-Scel site, and a chloroamphenicol cassette.
  • This intermediate targeting vector was digested together with l-Ceul and Pl-Scel and subsequently ligated into the modified mouse BAC clone (described above) to create the third targeting vector.
  • a third targeting vector for insertion of human ⁇ sequences into the endogenous ⁇ light chain locus which included, from 5' to 3', a 5' mouse homology arm containing ⁇ 23 kb of genomic sequence 5' of the endogenous mouse K locus, an l-Ceul site, a 5' Frt site, a neomycin cassette, a 3' Frt site, a -123 kb fragment containing the first 12 hV gene segments, a ⁇ 1 kb fragment containing ⁇ 1 , 2, 3 and 7 gene segments, a Pl-Scel site and a 3' homology arm containing -28 kb of mouse genomic sequence including the endogenous the mouse CK gene, ⁇ and ⁇ 3' and additional mouse genomic sequence downstream (3') of ⁇ 3' (FIG.
  • a human ⁇ mini-locus with an integrated human ⁇ light chain sequence [00233] A human ⁇ mini-locus with an integrated human ⁇ light chain sequence.
  • FIG. 4B two additional targeting vectors similar to those engineered to make an initial insertion of human ⁇ gene segments into the endogenous ⁇ light chain locus (FIG. 4B, 12/1 -K and 12/4- ⁇ Targeting Vectors) were engineered to progressively insert human ⁇ light chain gene segments using uniquely constructed targeting vectors containing contiguous human ⁇ and ⁇ genomic sequences. These targeting vectors were constructed to include a ⁇ 23 kb human ⁇ genomic sequence naturally located between human V 4-1 and JK1 gene segments. This human ⁇ genomic sequence was specifically positioned in these two additional targeting vectors between human V and human ⁇ gene segments (FIG. 4B, 12(K)1 -K and 12( ⁇ )4- ⁇ Targeting Vectors).
  • Both targeting vectors containing the human ⁇ genomic sequence were made using the modified RP1 1 -729g4 BAC clone described above (FIG. 6). This modified BAC clone was targeted with a spectinomycin selection cassette flanked by Notl and AsiSI restriction sites (FIG.6, top left).
  • a separate human BAC clone containing human ⁇ sequence (CTD-2366j12) was targeted two independent times to engineer restriction sites at locations between h 4-1 and hJKl gene segments to allow for subsequent cloning of a -23 kb fragment for ligation with the hV gene segments contained in the double targeted modified 729g4 BAC clone (FIG. 6, top right).
  • the 2366j12 BAC clone is about 132 kb in size and contains hVx gene segments 1 -6, 1 -5, 2-4, 7-3, 5-2, 4-1 , human ⁇ genomic sequence down stream of the VK gene segments, hJK gene segments 1 -5, the hCic and about 20 kb of additional genomic sequence of the human ⁇ locus.
  • This clone was first targeted with a targeting vector containing a hygromycin cassette flanked by Frt sites and a Notl site downstream (3') of the 3' Frt site.
  • the homology arms for this targeting vector contained human genomic sequence 5' and 3' of the VK gene segments within the BAC clone such that upon homologous recombination with this targeting vector, the VK gene segments were deleted and a Notl site was engineered -133 bp downstream of the h 4-1 gene segment (FIG. 6, top right).
  • This modified 2366j12 BAC clone was targeted independently with two targeting vectors at the 3' end to delete the IIJK gene segments with a chloroamphenicol cassette that also contained either a ⁇ gene segment, a Pl-Scel site and an AsiSI site or a human ⁇ genomic fragment containing four MX gene segments (supra), a Pl-Scel site and an AsiSI site (FIG.
  • the homology arms for these two similar targeting vectors contained sequence 5' and 3' of the hJK gene segments. Homologous recombination with these second targeting vectors and the modified 2366J12 BAC clone yielded a double- targeted 2366j12 clone which included, from 5' to 3', a 5' Frt site, a hygromycin cassette, a 3' Frt site, a Notl site, a 22,800 bp genomic fragment of the human ⁇ locus containing the intergenic region between the 4-1 and JK1 gene segments, either a ⁇ gene segment or a human ⁇ genomic fragment containing ⁇ 1 , ⁇ 2, JX3 and ⁇ 7, a Pl-Scel site and a chloroamphenicol cassette (FIG. 6, top right). Two final targeting vectors to make the two additional modifications were achieved by two ligation steps using the double-targeted 729g4 and 2366j12 clones.
  • Double targeted 729g4 and 2366j12 clones were digested with Notl and AsiSI yielding one fragment containing the neomycin cassette and hX ⁇ gene segments and another fragment containing the ⁇ 23 kb genomic fragment of the human ⁇ locus containing the intergenic region between the VK4-1 and JK1 gene segments, either a hJ 1 gene segment or a genomic fragment containing hJ 1 , J 2, ⁇ 3 and ⁇ 7 gene segments, the Pl- Scel site and the chloroamphenicol cassette, respectively.
  • BAC clones were then digested with l-Ceul and Pl-Scel to release the unique fragments containing the upstream neomycin cassette and the contiguous human ⁇ and ⁇ sequences and ligated into a modified mouse BAC clone 302g12 which contained from 5' to 3' mouse genomic sequence 5' of the endogenous ⁇ locus, an l-Ceul site, a 5' Frt site, a neomycin cassette, a 3' Frt site, hN ⁇ gene segments (3-12 to 3-1 ), a Notl site -200 bp downstream of ⁇ A3-1 , ⁇ 23 kb of human ⁇ sequence naturally found between the human VK4-1 and JK1 gene segments, either a ⁇ gene segment or a genomic fragment containing ⁇ , ⁇ 2, ⁇ 3 and JX7 gene segments, the mouse ⁇ , the mouse CK gene and ⁇ 3' (FIG.
  • Upstream (5 ) homology arms used in constructing targeting vectors for adding 16 additional hVX gene segments to the modified light chain loci described in Example 2 contained mouse genomic sequence 5' of either the endogenous ⁇ or ⁇ light chain loci.
  • the 3' homology arms were the same for all targeting vectors and contained human genomic sequence overlapping with the 5' end of the human ⁇ sequence of the modifications as described in Example 2.
  • FIG. 5A and 5B Two targeting vectors were engineered for introduction of 16 additional hV gene segments to the modified mouse light chain loci described in Example 2 (FIG. 5A and 5B, +16- ⁇ or +16- ⁇ Targeting Vector).
  • a ⁇ 172 kb DNA fragment from human BAC clone RP1 1-761113 (Invitrogen) containing 21 consecutive hVX gene segments from cluster A was engineered with a 5' homology arm containing mouse genomic sequence 5' to either the endogenous ⁇ or ⁇ light chain loci and a 3' homology arm containing human genomic ⁇ sequence.
  • the 5' mouse ⁇ or ⁇ homology arms used in these targeting constructs were the same 5' homology arms described in Example 2 (FIG. 5A and 5B).
  • the 3' homology arm included a 53,057 bp overlap of human genomic ⁇ sequence corresponding to the equivalent 5' end of the ⁇ 123 kb fragment of human genomic ⁇ sequence described in Example 2.
  • These two targeting vectors included, from 5' to 3', a 5' mouse homology arm containing either ⁇ 23 kb of genomic sequence 5' of the endogenous mouse ⁇ light chain locus or ⁇ 24 kb of mouse genomic sequence 5' of the endogenous ⁇ light chain locus, a 5' Frt site, a hygromycin cassette, a 3' Fit site and 171 ,457 bp of human genomic ⁇ sequence containing 21 consecutive ⁇ gene segments, ⁇ 53 kb of which overlaps with the 5' end of the human ⁇ sequence described in Example 3 and serves as the 3' homology arm for this targeting construct (FIG.
  • 5A and 5B +16- ⁇ or +16- ⁇ Targeting Vectors.
  • Homologous recombination with these targeting vectors created independently modified mouse ⁇ and ⁇ light chain loci each containing 28 hV gene segments and a hJ 1 gene segment operably linked to endogenous mouse constant genes (CK or CX2) which, upon recombination, leads to the formation of a chimeric light chain.
  • endogenous mouse constant genes CK or CX2
  • the +16- ⁇ Targeting Vector was also used to introduce the 16 additional hX ⁇ gene segments to the other initial modifications described in Example 2 that incorporated multiple ⁇ gene segments with and without an integrated human ⁇ sequence (FIG. 4B).
  • Homologous recombination with this targeting vector at the endogenous mouse ⁇ locus containing the other initial modifications created mouse ⁇ light chain loci containing 28 hN ⁇ gene segments and hJ 1 , 2, 3 and 7 gene segments with and without a human VK-JK genomic sequence operably linked to the endogenous mouse CK gene which, upon recombination, leads to the formation of a chimeric ⁇ - ⁇ light chain.
  • a targeting vector was engineered for introduction of 12 additional hX ⁇ gene segments to the modified mouse ⁇ and ⁇ light chain loci described above (FIG. 5A and 5B, +12- ⁇ or 2- ⁇ Targeting Vectors).
  • a 93,674 bp DNA fragment from human BAC clone RP1 1-22118 (Invitrogen) containing 12 consecutive hV gene segments from cluster B was engineered with a 5' homology arm containing mouse genomic sequence 5' to either the endogenous mouse ⁇ or ⁇ light chain loci and a 3' homology arm containing human genomic ⁇ sequence.
  • the 5' homology arms used in this targeting construct were the same 5' homology arms used for the addition of 16 hVX gene segments described above (FIG. 5A and 5B).
  • the 3' homology arm was made by engineering a Pl-Scel site ⁇ 3431 bp 5' to the human VX3-29P gene segment contained in a 27,468 bp genomic fragment of human ⁇ sequence from BAC clone RP1 1-761113.
  • This Pl-Scel site served as a ligation point to join the ⁇ 94 kb fragment of additional human ⁇ sequence to the ⁇ 27 kb fragment of human ⁇ sequence that overlaps with the 5' end of the human ⁇ sequence in the previous modification using the +16- ⁇ or +16- ⁇ Targeting Vectors (FIG.
  • 5A and 5B These two targeting vectors included, from 5' to 3', a 5' homology arm containing either ⁇ 23 kb of mouse genomic sequence 5' of the endogenous ⁇ light chain locus or ⁇ 24 kb of mouse genomic sequence 5' of the endogenous ⁇ light chain locus, a 5' Frt site, a neomycin cassette, a 3' Frt site and 121 ,188 bp of human genomic ⁇ sequence containing 16 hVX gene segments and a Pl-Scel site, ⁇ 27 kb of which overlaps with the 5' end of the human ⁇ sequence from the insertion of 16 addition hV gene segments and serves as the 3' homology arm for this targeting construct (FIG.
  • 5A and 5B +12- ⁇ or 12- ⁇ Targeting Vectors. Homologous recombination with these targeting vectors independently created modified mouse ⁇ and ⁇ light chain loci containing 40 hV gene segments and human ⁇ 1 operably linked to the endogenous mouse constant genes (CK or C 2) which, upon recombination, leads to the formation of a chimeric light chain (bottom of FIG.5A and 5B).
  • endogenous mouse constant genes CK or C 2
  • the +12- ⁇ Targeting Vector was also used to introduce the 12 additional hV gene segments to the other initial modifications that incorporated multiple hJ gene segments with and without an integrated human ⁇ sequence (FIG. 4B). Homologous recombination with this targeting vector at the endogenous mouse ⁇ locus containing the other modifications created a mouse ⁇ light chain locus containing 40 hV gene segments and ⁇ 1 , 2, 3 and 7 gene segments with and without a human VK-JK genomic sequence operably linked to the endogenous mouse CK gene which, upon recombination, leads to the formation of a chimeric ⁇ - ⁇ light chain.
  • Targeted BAC DNA made according to the foregoing Examples was used to electroporate mouse ES cells to create modified ES cells for generating chimeric mice that express human ⁇ light chain gene segments.
  • ES cells containing an insertion of unrearranged human ⁇ light chain gene segments were identified by a quantitative TAQMAN® assay.
  • Specific primers sets and probes were design for insertion of human ⁇ sequences and associated selection cassettes (gain of allele, GOA), loss of endogenous mouse sequences and any selection cassettes (loss of allele, LOA) and retention of flanking mouse sequences (allele retention, AR).
  • ES cells bearing the human ⁇ light chain gene segments are optionally transfected with a construct that expresses FLP in order to remove the Fifed neomycin cassette introduced by the insertion of the targeting construct containing human ⁇ 5-52 - V 1 -40 gene segments (FIG. 5A and 5B).
  • the neomycin cassette may optionally be removed by breeding to mice that express FLP recombinase (e.g., US 6,774,279). Optionally, the neomycin cassette is retained in the mice.
  • Targeted ES cells described above were used as donor ES cells and introduced into an 8-cell stage mouse embryo by the VELOCIMOUSE® method (see, e.g., US Pat. No. 7,294,754 and Poueymirou et al. (2007) F0 generation mice that are essentially fully derived from the donor gene-targeted ES cells allowing immediate phenotypic analyses Nature Biotech. 25(1 ):91-99.
  • VELOCIMICE® F0 mice fully derived from the donor ES cell
  • independently bearing human ⁇ gene segments were identified by genotyping using a modification of allele assay (Valenzuela et al., supra) that detected the presence of the unique human ⁇ gene segments (supra).
  • mice homozygous for each of three successive insertions of h ⁇ A, gene segments with a single hJ gene segment (FIG. 5B) and mice homozygous for a first insertion of hVX gene segments with either a single hJ gene segment or four human JX gene segments including a human VK-JK genomic sequence (FIG. 4B) were analyzed for ⁇ and ⁇ light chain expression in splenocytes using flow cytometry.
  • spleens were harvested from groups of mice (ranging from three to seven animals per group) and grinded using glass slides. Following lysis of red blood cells (RBCs) with ACK lysis buffer (Lonza Walkersville), splenocytes were stained with fluorescent dye conjugated antibodies specific for mouse CD19 (Clone 1 D3; BD Biosciences), mouse CD3 (17A2; Biolegend), mouse IgK (187.1 ; BD Biosciences) and mouse Ig (RML-42; Biolegend). Data was acquired using a BDTM LSR II flow cytometer (BD Biosciences) and analyzed using FLOWJOTM software (Tree Star, Inc.). Table 3 sets forth the average percent values for B cells (CD19 + ), ⁇ light chain and ⁇ light chain (CD19 + lg ⁇ lg + ) expression observed in splenocytes from groups of animals bearing each genetic modification.
  • FIG. 8A shows the ⁇ gX and Ig expression in CD19 + B cells for a representative mouse from each group. The number of CD19 + B cells per spleen was also recorded for each mouse (FIG. 8B).
  • B cell contents of the spleen and bone marrow compartments from mice homozygous for 40 hV and four hJ gene segments including a human VK-JK genomic sequence operably linked to the mouse CK gene were analyzed for progression through B cell development using flow cytometry of various cell surface markers.
  • RBCs from spleen and bone marrow preparations were lysed with ACK lysis buffer (Lonza Walkersville), followed by washing with complete RPMI medium. 1 x10 6 cells were incubated with anti-mouse CD16/CD32 (2.4G2, BD Biosciences) on ice for 10 minutes, followed by labeling with a selected antibody panel for 30 min on ice.
  • Bone marrow panel anti-mouse FITC-CD43 (1 B1 1 , BioLegend), PE-ckit (2B8, BioLegend), PeCy7-lgM (11/41 , eBioscience), PerCP-Cy5.5-lgD (1 1 -26c.2a, BioLegend), APC- B220 (RA3-6B2, eBioscience), APC-H7-CD19 (ID3, BD) and Pacific Blue-CD3 (17A2, BioLegend).
  • Bone marrow and spleen panel anti-mouse FITC-lgK (187.1 , BD), PE-lgX (RML-42, BioLegend), PeCy7-lgM (11/41 , ebioscience), PerCP-Cy5.5-lgD (1 1 -26c.2a, BioLegend), Pacific Blue-CD3 (17A2, BioLegend), APC- B220 (RA3-6B2, eBioscience), APC-H7-CD19 (ID3, BD).
  • FIGs. 9A - 9D show the results for the splenic compartment of one representative mouse from each group.
  • FIGs. 10A - 10E show the results for the bone marrow compartment of one representative mouse from each group.
  • Table 4 sets forth the average percent values for B cells (CD19 + ), ⁇ light chain (CD19 + lgK + lg ⁇ ), and ⁇ light chain (CD19 + lgK ⁇ lg + ) expression observed in splenocytes from groups of animals bearing various genetic modifications.
  • Table 5 sets forth the average percent values for B cells (CD19 + ), mature B cells (B220 hl lgM + ), immature B cells (B220 int lgM + ), immature B cells expressing ⁇ light chain (B220 int lgM + lgK + ) and immature B cells expressing ⁇ light chain (B220 int lgM + ⁇ + ) observed in bone marrow of wild type and mice homozygous for 40 hN ⁇ and four hJX gene segments including a human V -JK genomic sequence operably linked to the mouse CK gene. This experiment was repeated with additional groups of the mice described above and demonstrated similar results (data not shown).
  • mice bearing human ⁇ light chain gene segments bearing human ⁇ light chain gene segments.
  • Mice heterozygous for a first insertion of human ⁇ sequences ( ⁇ / ⁇ 3-12 - h ⁇ A.3-1 and hJ 1 , FIG. 5B) and homozygous for a third insertion of human ⁇ sequences (hV 5-52 - hV 3-1 and hJ 1 , FIG. 5B) were analyzed for human ⁇ light chain gene usage by reverse-transcriptase polymerase chain reaction (RT-PCR) using RNA isolated from splenocytes.
  • RT-PCR reverse-transcriptase polymerase chain reaction
  • spleens were harvested and perfused with 10 ml. RPMI-1640 (Sigma) with 5% HI-FBS in sterile disposable bags. Each bag containing a single spleen was then placed into a STOMACHERTM (Seward) and homogenized at a medium setting for 30 seconds. Homogenized spleens were filtered using a 0.7pm cell strainer and then pelleted with a centrifuge (1000 rpm for 10 minutes) and RBCs were iysed in BD PHARM LYSETM (BD Biosciences) for three minutes.
  • RT-PCR was performed on splenocyte RNA using primers specific for human hN/ ⁇ gene segments and the mouse CK gene (Table 6). PCR products were gel-purified and cloned into pCR2.1 -TOPO TA vector (Invitrogen) and sequenced with primers M13 Forward (GTAAAACGAC GGCCAG; SEQ ID NO:55) and M13 Reverse (CAGGAAACAG CTATGAC; SEQ ID NO:56) located within the vector at locations flanking the cloning site. Eighty-four total clones derived from the first and third insertions of human ⁇ sequences were sequenced to determine hX ⁇ gene usage (Table 7). The nucleotide sequence of the hV -hJ 1-mCK junction for selected RT-PCR clones is shown in FIG. 1 1.
  • mice homozygous for a third insertion of human ⁇ light chain gene sequences i.e. 40 hN ⁇ gene segments and four hJX gene segments including a human VK-JK genomic sequence, bottom of FIG. 7B
  • human ⁇ light chain gene sequences i.e. 40 hN ⁇ gene segments and four hJX gene segments including a human VK-JK genomic sequence, bottom of FIG. 7B
  • mice homozygous for a third insertion of human ⁇ light chain gene sequences i.e. 40 hN ⁇ gene segments and four hJX gene segments including a human VK-JK genomic sequence, bottom of FIG. 7B
  • mice homozygous for a third insertion of human ⁇ light chain gene sequences i.e. 40 hN ⁇ gene segments and four hJX gene segments including a human VK-JK genomic sequence, bottom of FIG. 7B
  • mice homozygous for a third insertion of human ⁇ light chain gene sequences i
  • mice homozygous for a first insertion of human ⁇ light chain gene segments (12 hVX gene segments and hJ 1 , FIG. 4A & FIG. 5A) operably linked to the endogenous mouse ⁇ 2 gene were analyzed for human ⁇ light chain gene usage by RT-PCR using RNA isolated from splenocytes (as described above).
  • the primers specific for hVX gene segments (Table 6) were paired with one of two primers specific for the mouse CX2 gene; CX2-1 (SEQ ID NO:104) or C 2-2 (SEQ ID NO: 105).
  • hN ⁇ gene segments rearranged to h 1 were observed from the RT- PCR clones from mice bearing human ⁇ light chain gene segments at the endogenous mouse ⁇ light chain locus.
  • the nucleotide sequence of the hVX-hJX-m ⁇ 2 junction for selected RT-PCR clones is shown in FIG. 13.
  • FIG. 1 1 shows the sequence of the ⁇ / ⁇ - ⁇ 1- ⁇ " ⁇ junction for RT-PCR clones from mice bearing a first and third insertion of hX ⁇ gene segments with a single hJ gene segment.
  • the sequences shown in FIG. 1 1 illustrate unique rearrangements involving different hN ⁇ gene segments with hJX1 recombined to the mouse CK gene.
  • Heterozygous mice bearing a single modified endogenous ⁇ locus containing 12 hN/ ⁇ gene segments and hJ 1 and homozygous mice bearing two modified endogenous ⁇ loci containing 40 hN ⁇ gene segments and ⁇ 1 were both able to produce human ⁇ gene segments operably linked to the mouse CK gene and produce B cells that expressed human ⁇ light chains. These rearrangements demonstrate that the chimeric loci were able to independently rearrange human ⁇ gene segments in multiple, independent B cells in these mice.
  • mice made functional antibodies containing rearranged human ⁇ / ⁇ - ⁇ gene segments operably linked to mouse CK genes as part of the endogenous immunoglobulin light chain repertoire.
  • FIG. 12 shows the sequence of the junction for selected RT-PCR clones from mice homozygous for 40 hX ⁇ and four ⁇ gene segments including a human VK-JK genomic sequence.
  • the sequences shown in FIG. 12 illustrate additional unique rearrangements involving multiple different hX ⁇ gene segments, spanning the entire chimeric locus, with multiple different ⁇ gene segments rearranged and operably linked to the mouse CK gene.
  • Homozygous mice bearing modified endogenous ⁇ loci containing 40 hVX and four J gene segments were also able to produce human ⁇ gene segments operably linked to the mouse CK gene and produce B cells that expressed human ⁇ light chains.
  • mice as well made functional antibodies containing human ⁇ / ⁇ - ⁇ gene segments operably linked to mouse CK regions as part of the endogenous immunoglobulin light chain repertoire.
  • FIG. 13 shows the sequence of the hV -hJ -mC 2 junction for three individual RT-PCR clones from mice homozygous for 12 hN ⁇ gene segments and hJ 1 .
  • One clone demonstrated a nonproductive rearrangement due to N additions at the hV -hJ junction (2D1 , FIG.13).
  • mice bearing modified endogenous ⁇ loci containing 12 hX ⁇ gene segments and hJX1 were also able to produce human ⁇ gene segments operably linked to an endogenous mouse C gene and produce B cells that expressed reverse chimeric ⁇ light chains containing hV regions linked to mouse C regions.
  • These rearrangements further demonstrate that human ⁇ light chain gene segments placed at the other light chain locus ⁇ i.e., the ⁇ locus) were able to independently rearrange human ⁇ gene segments in multiple, independent B cells in these mice.
  • mice also made functional antibodies containing human ⁇ - ⁇ gene segments operably linked to a mouse ⁇ region as part of the endogenous immunoglobulin light chain repertoire.
  • mice bearing human ⁇ light chain gene segments at the endogenous ⁇ and ⁇ light chain loci are capable of rearranging human ⁇ light chain gene segments and expressing them in the context of a mouse CK and/or C region as part of the normal antibody repertoire of the mouse because a functional light chain is required at various checkpoints in B cell development in both the spleen and bone marrow.
  • early subsets of B cells e.g., pre-, pro- and transitional B cells
  • mice bearing the unrearranged human ⁇ gene segments are bred to another mouse containing a deletion in the opposing endogenous light chain locus (either ⁇ or ⁇ ).
  • a deletion in the opposing endogenous light chain locus either ⁇ or ⁇
  • human ⁇ gene segments positioned at the endogenous ⁇ locus would be the only functional light chain gene segments present in a mouse that also carried a deletion in the endogenous ⁇ light chain locus.
  • the progeny obtained would express only human ⁇ light chains as described in the foregoing examples. Breeding is performed by standard techniques recognized in the art and, alternatively, by commercial companies, e.g., The Jackson Laboratory.
  • Mouse strains bearing human ⁇ light chain gene segments at the endogenous ⁇ locus and a deletion of the endogenous ⁇ light chain locus are screened for presence of the unique reverse-chimeric (human-mouse) ⁇ light chains and absence of endogenous mouse ⁇ light chains.
  • mice bearing an unrearranged human ⁇ light chain locus are also bred with mice that contain a replacement of the endogenous mouse heavy chain variable gene locus with the human heavy chain variable gene locus (see US 6,596,541 , Regeneron Pharmaceuticals, the VELOCIMMUNE® genetically engineered mouse).
  • VELOCIMMUNE® mouse includes, in part, having a genome comprising human heavy chain variable regions operably linked to endogenous mouse constant region loci such that the mouse produces antibodies comprising a human heavy chain variable region and a mouse heavy chain constant region in response to antigenic stimulation.
  • the DNA encoding the variable regions of the heavy chains of the antibodies can be isolated and operably linked to DNA encoding the human heavy chain constant regions.
  • the DNA can then be expressed in a cell capable of expressing the fully human heavy chain of the antibody.
  • mice bearing a replacement of the endogenous mouse heavy chain locus with the human heavy chain locus and an unrearranged human ⁇ light chain locus at the endogenous ⁇ light chain locus is obtained.
  • Antibodies containing somatically mutated human heavy chain variable regions and human ⁇ light chain variable regions can be isolated upon immunization with an antigen of interest.
  • mice that contain the unrearranged human ⁇ light chain locus are immunized with an antigen of interest.
  • a VELOCIMMUNE® mouse containing one of the single rearranged human germline light chain regions is challenged with an antigen, and lymphatic cells (such as B-cells) are recovered from serum of the animals.
  • lymphatic cells such as B-cells
  • the lymphatic cells may be fused with a myeloma cell line to prepare immortal hybridoma cell lines, and such hybridoma cell lines are screened and selected to identify hybridoma cell lines that produce antibodies containing human heavy chain and human ⁇ light chain that are specific to the antigen used for immunization.
  • DNA encoding the variable regions of the heavy chains and the ⁇ light chains may be isolated and linked to desirable isotypic constant regions of the heavy chain and light chain.
  • the diversity of the light chain repertoire is dramatically increased and confers higher diversity on the antigen-specific repertoire upon immunization.
  • the resulting cloned antibody sequences may be subsequently produced in a cell, such as a CHO cell.
  • DNA encoding the antigen-specific chimeric antibodies or the variable domains of the light and heavy chains may be isolated directly from antigen-specific lymphocytes (e.g., B cells).
  • high affinity chimeric antibodies are isolated having a human variable region and a mouse constant region. As described above, the antibodies are
  • mouse constant regions are replaced with a desired human constant region to generate the fully human antibody containing a somatically mutated human heavy chain and a human ⁇ light chain derived from an unrearranged human ⁇ light chain locus of the invention.
  • Suitable human constant regions include, for example wild type or modified lgG1 , lgG2, lgG3, or lgG4.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Biomedical Technology (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Environmental Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Microbiology (AREA)
  • Biodiversity & Conservation Biology (AREA)
  • Animal Husbandry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Physics & Mathematics (AREA)
  • Plant Pathology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Reproductive Health (AREA)
  • Gynecology & Obstetrics (AREA)
  • Developmental Biology & Embryology (AREA)
  • Cell Biology (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Position Input By Displaying (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
  • Medicines Containing Plant Substances (AREA)

Abstract

Genetically modified mice are provided that express human λ variable (hVλ) sequences, including mice that express hVλ sequences from an endogenous mouse λ light chain locus, mice that express hVλ sequences from an endogenous mouse κ light chain locus, and mice that express hVλ sequences from a transgene or an episome wherein the hVλ sequence is linked to a mouse constant sequence. Mice are provided that are a source of somatically mutated human λ variable sequences useful for making antigen- binding proteins. Compositions and methods for making antigen-binding proteins that comprise human λ variable sequences, including human antibodies, are provided.

Description

MICE EXPRESSING ALIGHT CHAIN WITH HUMAN LAMBDA VARIABLE AND MOUSE CONSTANT REGIONS
FIELD
[0001] Genetically modified mice that comprise a mouse or human lambda variable (\ λ) light chain sequence operably linked with a mouse or human light chain constant region (λ or kappa(i)). Genetically modified mice that express epitope-binding proteins that comprise an immunoglobulin light chain comprising a variable domain derived from a human lambda variable (hX λ) gene segment, a human lambda J (hJ ) gene segment, and a mouse light chain constant (CL) domain. Genetically modified mice, comprising an unrearranged immunoglobulin lambda (λ) light chain variable nucleic acid sequence at an endogenous mouse light chain locus. Mice capable of rearranging and expressing a chimeric human λ/mouse CL light chain from an endogenous light chain locus that comprises a replacement of all endogenous mouse light chain variable region gene segments with one or more hV gene segments and one or more ηϋλ gene segments. Somatically mutated antibodies comprising hN/λ domains and mouse CL domains.
BACKGROUND
[0002] Mice that express antibodies that are fully human, or partly human and partly mouse, are known in the art. For example, transgenic mice that express fully human antibodies from transgenes containing human light and heavy chain immunoglobulin variable region genes have been reported. Genetically modified mice that comprise a replacement of the endogenous mouse heavy chain variable region (HCVR) gene segments and kappa (κ) light chain variable region (LCVR) gene segments with human HCVR and LCVR gene segments and that make chimeric antibodies with a chimeric human/mouse kappa chain are known as well.
[0003] Antibody light chains are encoded by one of two separate loci: kappa (κ) and lambda (λ). Mouse antibody light chains are primarily of the κ type. The ratio of κ to λ light chain usage in humans is about 60:40, whereas in mice it is about 95:5. Biased usage of κ light chains in mice is reportedly sustained in genetically modified mice capable of expressing fully or partly human antibodies. Thus, mice that express fully or partly human antibodies appear to be constrained in lambda variable usage.
[0004] There is a need in the art to generate lambda variable regions, whether mouse or human, for use in making epitope-binding proteins. There is a need in the art for mice that express fully or partly human antibodies, wherein the mice display an increased lambda variable (νλ) usage. [0005] There is a need in the art for mice that express fully or partly human antibodies, wherein the mice display an increased λ variable (\/λ) usage.
SUMMARY
[0006] Genetically modified mice, embryos, cells, tissues, as well as nucleic acid constructs for modifying mice, and methods and compositions for making and using them, are provided. Mice and cells that generate lambda (λ) variable regions (human or non- human) in the context of a kappa (κ) light chain are provided. Mice and cells that generate human λ variable regions in the context of a κ or a λ light chain, e.g. , from an endogenous mouse light chain locus, are also provided. Also provided are methods for making antibodies that comprise lambda variable regions. Methods for selecting heavy chains that express with cognate lambda variable regions are also provided.
[0007] Chimeric and human antigen-binding proteins (e.g., antibodies), and nucleic acids encoding them, are provided that comprise somatically mutated variable regions, including antibodies that have light chains comprising a variable domain derived from a human νλ and a human ϋλ gene segment fused to a mouse light chain constant domain.
[0008] In one aspect, a mouse is provided that expresses a human λ variable region sequence on a light chain that comprises a mouse constant region. In one aspect, a mouse is provided that expresses a human λ variable region sequence on a light chain that comprises a κ constant region. In one aspect, a mouse is provided that expresses from an endogenous mouse light chain locus a light chain that comprises a human λ variable region sequence. In one aspect, a mouse is provided that comprises a rearranged light chain gene that comprises a human λ variable sequence linked to a mouse constant region sequence; in one embodiment, the mouse constant region sequence is a λ constant sequence; in one embodiment, the mouse constant region sequence is a κ constant sequence.
[0009] In one aspect, a genetically modified mouse is provided, wherein the mouse comprises an unrearranged human λ light chain variable gene segment (hN λ) and a human λ joining gene segment (hJX). In one embodiment, the unrearranged hVX and hJ are at a mouse light chain locus. In one embodiment, the unrearranged hN λ and unrearranged hJ are on a transgene and operably linked to a human or mouse constant region sequence. In one embodiment, the unrearranged hV and unrearranged ηϋλ are on an episome. In one embodiment, the mouse is capable of making an immunoglobulin that comprises a light chain that is derived from an unrearranged hN λ sequence and a ηϋλ sequence and a mouse light chain constant region (CL) nucleic acid sequence. Methods and compositions for making and using genetically modified mice are also provided. Antibodies are provided that comprise (a) a human heavy chain variable domain (hVH) fused to a mouse heavy chain constant region, and (b) a human νλ fused to a mouse CL domain; including wherein one or more of the variable domains are somatically mutated, e.g. , during antibody or immune cell selection in a mouse of the invention. In one embodiment, the unrearranged hX λ and unrearranged hJ are operably linked with a human or mouse κ constant region (CK). In one embodiment, the unrearranged hX λ and unrearranged hJX are operably linked with a human or mouse λ constant region (Ολ).
[0010] In one aspect, a mouse is provided that comprises in its germline, at an endogenous mouse light chain locus, a human λ light chain variable region sequence, wherein the human lambda variable region sequence is expressed in a light chain that comprises a mouse immunoglobulin constant region gene sequence.
[0011] In one embodiment, the endogenous mouse light chain locus is a λ locus. In one embodiment, the endogenous mouse light chain locus is a κ locus.
[0012] In one embodiment, the mouse lacks an endogenous light chain variable sequence at the endogenous mouse light chain locus.
[0013] In one embodiment, all or substantially all endogenous mouse light chain variable region gene segments are replaced with one or more human λ variable region gene segments.
[0014] In one embodiment, the human λ light chain variable region sequence comprises a human ϋλ sequence. In one embodiment, the human ϋλ sequence is selected from the group consisting of ϋλ1 , ϋλ2, ϋλ3, JX7, and a combination thereof.
[0015] In one embodiment, the human λ light chain variable region sequence comprises a fragment of cluster A of the human light chain locus. In a specific
embodiment, the fragment of cluster A of the human λ light chain locus extends from hV 3- 27 through hV 3-1 .
[0016] In one embodiment, the human λ light chain variable region sequence comprises a fragment of cluster B of the human light chain locus. In a specific
embodiment, the fragment of cluster B of the human λ light chain locus extends from ηνλ5- 52 through hVX1 -40.
[0017] In one embodiment, the human λ light chain variable region sequence comprises a genomic fragment of cluster A and a genomic fragment of cluster B. In a one embodiment, the human λ light chain variable region sequence comprises at least one gene segment of cluster A and at least one gene segment of cluster B.
[0018] In one embodiment, more than 10% of the light chain naive repertoire of the mouse is derived from at least two hN λ gene segments selected from 2-8, 2-23, 1 -40, 5-45, and 9-49. In one embodiment, more than 20% of the light chain naive repertoire of the mouse is derived from at least three hX λ gene segments selected from 2-8, 2-23, 1-40, 5- 45, and 9-49. In one embodiment, more than 30% of the light chain naive repertoire of the mouse is derived from at least four hV gene segments selected from 2-8, 2-23, 1 -40, 5- 45, and 9-49.
[0019] In one aspect, a mouse is provided that expresses an immunoglobulin light chain that comprises a human λ variable sequence fused with a mouse constant region, wherein the mouse exhibits a κ usage to λ usage ratio of about 1 :1.
[0020] In one embodiment, the immunoglobulin light chain is expressed from an endogenous mouse light chain locus.
[0021] In one aspect, a mouse is provided that comprises a λ light chain variable region sequence (Ν λ) and at least one J sequence (J), contiguous with a mouse κ light chain constant region sequence.
[0022] In one embodiment, the mouse lacks a functional mouse VK and/or mouse JK gene segment.
[0023] In one embodiment, the \ λ is a human \/λ (hN/λ), and the J is a human ϋλ (hJ ). In one embodiment, the hX λ and the ηϋλ are unrearranged gene segments.
[0024] In one embodiment, the mouse comprises a plurality of unrearranged hN λ gene segments and at least one hJk gene segment. In a specific embodiment, the plurality of unrearranged hN/λ gene segments are at least 12 gene segments, at least 28 gene segments, or at least 40 gene segments.
[0025] In one embodiment, the at least one hJ gene segment is selected from the group consisting of ϋλ1 , ϋλ2, ϋλ3, ϋλ7, and a combination thereof.
[0026] In one embodiment, an endogenous mouse λ light chain locus is deleted in whole or in part.
[0027] In one embodiment, the mouse κ light chain constant region sequence is at an endogenous mouse κ light chain locus.
[0028] In one embodiment, about 10% to about 45% of the B cells of the mouse express an antibody that comprises a light chain comprising a human λ light chain variable (\/λ) domain and a mouse κ light chain constant (CK) domain.
[0029] In one embodiment, the human λ variable domain is derived from a rearranged hVX/hJ sequence selected from the group consisting of 3-1/1 , 3-1/7, 4-3/1 , 4-3/7, 2-8/1 , 3- 9/1 , 3-10/1 , 3-10/3, 3-10/7, 2-14/1 , 3-19/1 , 2-23/1 , 3-25/1 , 1-40/1 , 1 -40/2, 1-40/3, 1-40/7, 7- 43/1 , 7-43/3, 1-44/1 , 1 -44/7, 5-45/1 , 5-45/2, 5-45/7, 7-46/1 , 7-46/2, 7-46/7, 9-49/1 , 9-49/2, 9-49/7 and 1 -51/1 .
[0030] In one embodiment, the mouse further comprises a human VK-JK intergenic region from a human κ light chain locus, wherein the human VK-JK intergenic region is contiguous with the VX sequence and the J sequence. In a specific embodiment, the human VK-JK intergenic region is placed between the VX sequence and the J sequence.
[0031] In one aspect, a mouse is provided that comprises (a) at least 12 to at least 40 unrearranged human λ light chain variable region gene segments and at least one human JX gene segment at an endogenous mouse light chain locus; (b) a human VK-JK intergenic sequence located between the at least 12 to at least 40 human light chain variable region gene segments and the at least one human JX sequence; wherein the mouse express an antibody that comprises a light chain comprising a human νλ domain and a mouse CK domain.
[0032] In one aspect, a mouse is provided that expresses an antibody comprising a light chain that comprises a λ variable sequence and a κ constant sequence.
[0033] In one embodiment, the mouse exhibits a κ usage to λ usage ratio of about 1 : 1 .
[0034] In one embodiment, a population of immature B cells obtained from bone marrow of the mouse exhibits a κ usage to λ usage ratio of about 1 : 1 .
[0035] In one aspect, a genetically modified mouse is provided, wherein the mouse comprises an unrearranged immunoglobulin νλ and a JX gene segment operably linked to a mouse light chain locus that comprises a mouse CL gene.
[0036] In one embodiment, the VX and/or JX gene segments are human gene segments. In one embodiment, the νλ and/or JX gene segments are mouse gene segments, and the CL is a mouse CK.
[0037] In one embodiment, the endogenous mouse light chain locus is a κ light chain locus. In one embodiment, the endogenous mouse light chain locus is a λ light chain locus.
[0038] In one embodiment, the unrearranged VX and JX gene segments are at an endogenous mouse light chain locus.
[0039] In one embodiment, the unrearranged immunoglobulin νλ and JX gene segments are on a transgene.
[0040] In one embodiment, the mouse further comprises a replacement of one or more heavy chain V, D, and/or J gene segments with one or more human V, D, and/or J gene segments at an endogenous mouse heavy chain immunoglobulin locus.
[0041] In one embodiment, the mouse comprises an unrearranged immunoglobulin VX and a JX gene segment at an endogenous mouse κ light chain locus that comprises a mouse CK gene. [0042] In one embodiment, the mouse comprises an unrearranged human
immunoglobulin λ light chain variable gene segment (νλ) and a λ joining gene segment (ϋλ) at an endogenous mouse λ light chain locus that comprises a mouse CX gene.
[0043] In one embodiment, the light chain variable gene locus (the "VL locus") comprises at least one human VX (hVX) gene segment. In one embodiment, the VL locus comprises at least one human JX (hJX) gene segment. In another embodiment, VL locus comprises up to four hJX gene segments. In one embodiment, the VL locus comprises a contiguous sequence comprising human λ and human κ genomic sequence.
[0044] In one embodiment, the κ light chain variable gene locus (the "κ locus") comprises at least one human VX (hVX) gene segment. In one embodiment, the κ locus comprises at least one human ϋλ (hJX) gene segment. In one embodiment, the κ locus comprises up to four hJX gene segments. In one embodiment, the κ locus comprises at least one hVX and at least one hJX, and lacks or substantially lacks a functional VK region gene segment and lacks or substantially lacks a functional JK region gene segment. In one embodiment, the mouse comprises no functional VK region gene segment. In one embodiment, the mouse comprises no functional JK region gene segment.
[0045] In one embodiment, the λ light chain variable gene locus (the "λ locus") comprises at least one hVX gene segment. In one embodiment, the λ locus comprises at least one human JX (hJX) gene segment. In another embodiment, the X locus comprises up to four hJX gene segments.
[0046] In one embodiment, the VL locus comprises a plurality of hVXs. In one embodiment, the plurality of hVXs are selected so as to result in expression of a X light chain variable region repertoire that reflects about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, or about 90% or more of the VX usage observed in a human. In one embodiment, the VL locus comprises gene segments hVX 1-40, 1-44, 2-8, 2-14, 3-21 , and a combination thereof.
[0047] In one embodiment, the hVXs include 3-1 , 4-3, 2-8, 3-9, 3-10, 2-11 , and 3-12. In a specific embodiment, the VL locus comprises a contiguous sequence of the human X light chain locus that spans from VX3-12 to VX3-1. In one embodiment, the VL locus comprises at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1 or 12 hVXs. In a specific embodiment, the hVXs include 3-1 , 4-3, 2-8, 3-9, 3-10, 2-1 1 , and 3-12. In a specific embodiment, the VL locus comprises a contiguous sequence of the human X locus that spans from VX3-12 to VX3-1. In one embodiment, the VL locus is at the endogenous κ locus. In a specific embodiment, the VL locus is at the endogenous κ locus and the endogenous X light chain locus is deleted in part or completely. In one embodiment, the VL locus is at the endogenous λ locus. In a specific embodiment, the VL locus is at the endogenous λ locus and the endogenous κ locus is deleted in part or completely.
[0048] In one embodiment, the VL locus comprises 13 to 28 or more hV s. In a specific embodiment, the hV s include 2-14, 3-16, 2-18, 3-19, 3-21 , 3-22, 2-23, 3-25, and 3-27. In a specific embodiment, the κ locus comprises a contiguous sequence of the human λ locus that spans from ΜλΖ-21 to \ λ3-1. In one embodiment, the VL locus is at the endogenous κ locus. In a specific embodiment, the VL locus is at the endogenous κ locus and the endogenous λ light chain locus is deleted in part or completely. In another embodiment, the VL locus is at the endogenous λ locus. In a specific embodiment, the VL locus is at the endogenous λ locus and the endogenous κ locus is deleted in part or completely.
[0049] In one embodiment, the VL locus comprises 29 to 40 hV s. In a specific embodiment, the κ locus comprises a contiguous sequence of the human λ locus that spans from \/λ3-29 to \/λ3-1 , and a contiguous sequence of the human λ locus that spans from V 5-52 to νλ1-40. In a specific embodiment, all or substantially all sequence between hV 1-40 and ΙΆ/λ3-29 in the genetically modified mouse consists essentially of a human λ sequence of approximately 959 bp found in nature (e.g., in the human population) downstream of the ΙΆ/λ1-40 gene segment (downstream of the 3' untranslated portion), a restriction enzyme site (e.g., Pl-Scel), followed by a human λ sequence of approximately 3,431 bp upstream of the hV 3-29 gene segment found in nature. In one embodiment, the VL locus is at the endogenous mouse κ locus. In a specific embodiment, the VL locus is at the endogenous mouse κ locus and the endogenous mouse λ light chain locus is deleted in part or completely. In another embodiment, the VL locus is at the endogenous mouse λ locus. In a specific embodiment, the VL locus is at the endogenous mouse λ locus and the endogenous mouse κ locus is deleted in part or completely.
[0050] In one embodiment, the VL locus comprises at least one hJ . In one
embodiment, the VL locus comprises a plurality of hJ s. In one embodiment, the VL locus comprises at least 2, 3, 4, 5, 6, or 7 hJX. In a specific embodiment, the VL locus comprises four hJ . In a specific embodiment, the four hJ s are Ιιϋλΐ , hJ 2, hJX3, and Ιιϋλ7. In one embodiment, the VL locus is a κ locus. In a specific embodiment, the VL locus is at the endogenous κ locus and the endogenous λ light chain locus is deleted in part or completely. In one embodiment, the VL locus comprises one hJX. In a specific
embodiment, the one hJ is hJ 1 . In one embodiment, the VL locus is at the endogenous K locus. In a specific embodiment, the VL locus is at the endogenous locus and the endogenous λ light chain locus is deleted in part or completely. In another embodiment, the VL locus is at the endogenous λ locus. In a specific embodiment, the VL locus is at the endogenous λ locus and the endogenous κ locus is deleted in part or completely.
[0051] In one embodiment, the VL locus comprises at least one hN λ, at least one bJk, and a mouse CK gene. In one embodiment, the VL locus comprises at least one h\A,, at least one hJ , and a mouse Ck gene. In a specific embodiment, the mouse Ck gene is Ck2. In a specific embodiment, the mouse Ck gene is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, 96%, 97%, 98%, or at least 99% identical to mouse Ck2.
[0052] In one embodiment, the mouse comprises a replacement at the endogenous mouse K locus of endogenous mouse VK gene segments with one or more hVX gene segments, wherein the hV gene segments are operably linked to an endogenous mouse CK region gene, such that the mouse rearranges the human νλ gene segments and expresses a reverse chimeric immunoglobulin light chain that comprises a human νλ domain and a mouse CK. In one embodiment, 90-100% of unrearranged mouse VK gene segments are replaced with at least one unrearranged hN/λ gene segment. In a specific embodiment, all or substantially all of the endogenous mouse VK gene segments are replaced with at least one unrearranged hV gene segment. In one embodiment, the replacement is with at least 12, at least 28, or at least 40 unrearranged hV gene segments. In one embodiment, the replacement is with at least 7 functional unrearranged hV gene segments, at least 16 functional unrearranged hV gene segments, or at least 27 functional unrearranged hVk gene segments. In one embodiment, the mouse comprises a replacement of all mouse JK gene segments with at least one unrearranged hJX gene segment. In one embodiment, the at least one unrearranged bJk gene segment is selected from ϋλ1 , Jk2, J 3, ϋλ4, ϋλ5, ϋλ6, JX7, and a combination thereof. In a specific embodiment, the one or more A λ gene segment is selected from a 3-1 , 4-3, 2-8, 3-9, 3- 10, 2-11 , 3-12, 2-14, 3-16, 2-18, 3-19, 3-21 , 3-22, 2-23, 3-25, 3-27, 1-40, 7-43, 1 -44, 5-45, 7-46, 1-47, 5-48, 9-49, 1 -50, 1 -51 , a 5-52 hV gene segment, and a combination thereof. In a specific embodiment, the at least one unrearranged ηϋλ gene segment is selected from ϋλ1 , ϋλ2, ϋλ3, ϋλ7, and a combination thereof.
[0053] In one embodiment, the mouse comprises a replacement of endogenous mouse νλ gene segments at the endogenous mouse λ locus with one or more human νλ gene segments at the endogenous mouse λ locus, wherein the hVk gene segments are operably linked to a mouse Ck region gene, such that the mouse rearranges the hVX gene segments and expresses a reverse chimeric immunoglobulin light chain that comprises a hVX domain and a mouse Ck. In a specific embodiment, the mouse Ck gene is Ck2. In a specific embodiment, the mouse Ck gene is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse C 2. In one embodiment, 90- 100% of unrearranged mouse νλ gene segments are replaced with at least one
unrearranged hX λ gene segment. In a specific embodiment, all or substantially all of the endogenous mouse νλ gene segments are replaced with at least one unrearranged hX λ gene segment. In one embodiment, the replacement is with at least 12, at least 28, or at least 40 unrearranged hN λ gene segments. In one embodiment, the replacement is with at least 7 functional unrearranged hN λ gene segments, at least 16 functional unrearranged hN/λ gene segments, or at least 27 functional unrearranged hVX gene segments. In one embodiment, the mouse comprises a replacement of all mouse ϋλ gene segments with at least one unrearranged hJ gene segment. In one embodiment, the at least one unrearranged Ιιϋλ gene segment is selected from ϋλ1 , ϋλ2, JX3, ϋλ4, ϋλ5, ϋλδ, ϋλ7, and a combination thereof. In a specific embodiment, the one or more hN/λ gene segment is selected from a 3-1 , 4-3, 2-8, 3-9, 3-10, 2-1 1 , 3-12, 2-14, 3-16, 2-18, 3-19, 3-21 , 3-22, 2- 23, 3-25, 3-27, 1 -40, 7-43, 1 -44, 5-45, 7-46, 1 -47, 5-48, 9-49, 1 -50, 1 -51 , a 5-52 hV gene segment, and a combination thereof. In a specific embodiment, the at least one
unrearranged hJ gene segment is selected from ϋλ1 , JX2, JX3, ϋλ7, and a combination thereof.
[0054] In one aspect, a genetically modified mouse is provided that comprises a human VK-JK intergenic region sequence located at an endogenous mouse κ light chain locus.
[0055] In one embodiment, the human VK-JK intergenic region sequence is at an endogenous κ light chain locus of a mouse that comprises a hX λ and hJ gene segment, and the human VK-JK intergenic region sequence is disposed between the hV and hJ gene segments. In a specific embodiment, the hA/λ and hJ gene segments are capable of recombining to form a functional human λ light chain variable domain in the mouse.
[0056] In one embodiment, a mouse is provided that comprises a plurality of hV 's and one or more J 's, and the human VK-JK intergenic region sequence is disposed, with respect to transcription, downstream of the proximal or 3' most hV sequence and upstream or 5' of the first J sequence.
[0057] In one embodiment, the human VK-JK intergenic region is a region located about 130 bp downstream or 3' of a human VK4-1 gene segment, about 130 bp
downstream of the 3' untranslated region of the human 4-1 gene segment, and spans to about 600 bp upstream or 5' of a human JK1 gene segment. In a specific embodiment, the human VK-JK intergenic region is about 22.8 kb in size. In one embodiment, the VK-JK intergenic region is about 90% or more, 91 % or more, 92% or more, 93% or more, 94% or more, or about 95% or more identical with a human VK-JK intergenic region extending from the end of the 3' untranslated region of a human VK4-1 gene segment to about 600 bp upstream of a human JK1 gene segment. In one embodiment, the VK-JK intergenic region comprises SEQ ID NO: 1 00. In a specific embodiment, the VK-JK intergenic region comprises a functional fragment of SEQ ID NO: 100. In a specific embodiment, the VK-JK intergenic region is SEQ ID NO: 1 00.
[0058] In one aspect, a mouse, a mouse cell (e.g., a mouse embryonic stem cell), a mouse embryo, and a mouse tissue are provided that comprise the recited human VK-JK intergenic region sequence, wherein the intergenic region sequence is ectopic. In a specific embodiment, the ectopic sequence is placed at a humanized endogenous mouse immunoglobulin locus.
[0059] In one aspect, an isolated nucleic acid construct is provided that comprises the recited human VK-JK intergenic region sequence. In one embodiment, the nucleic acid construct comprises targeting arms to target the human VK-JK intergenic region sequence to a mouse light chain locus. In a specific embodiment, the mouse light chain locus is a κ locus. In a specific embodiment, the targeting arms target the human VK-JK intergenic region to a modified endogenous mouse κ locus, wherein the targeting is to a position between a hV sequence and a hJ sequence.
[0060] In one aspect, a genetically modified mouse is provided, wherein the mouse comprises no more than two light chain alleles, wherein the light chain alleles comprise (a) an unrearranged immunoglobulin human V and a JX gene segment at an endogenous mouse light chain locus that comprises a mouse CL gene; and, (b) an unrearranged immunoglobulin VL and a JL gene segment at an endogenous mouse light chain locus that comprises a mouse CL gene.
[0061] In one embodiment, the endogenous mouse light chain locus is a κ locus. In another embodiment, the endogenous mouse light chain locus is a λ locus.
[0062] In one embodiment, the no more than two light chain alleles are selected from a
K allele and a λ allele, two κ alleles, and two λ alleles. In a specific embodiment, one of the two light chain alleles is a λ allele that comprises a 0 2 gene.
[0063] In one embodiment, the mouse comprises one functional immunoglobulin light chain locus and one nonfunctional light chain locus, wherein the functional light chain locus comprises an unrearranged immunoglobulin human νλ and a gene segment at an endogenous mouse κ light chain locus that comprises a mouse CK gene.
[0064] In one embodiment, the mouse comprises one functional immunoglobulin light chain locus and one nonfunctional light chain locus, wherein the functional light chain locus comprises an unrearranged immunoglobulin human νλ and a όλ gene segment at an endogenous mouse λ light chain locus that comprises a mouse CX gene. In one embodiment, the CX gene is CX2. In a specific embodiment, the mouse CX gene is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse CX2.
[0065] In one embodiment, the mouse further comprises at least one immunoglobulin heavy chain allele. In one embodiment, the at least one immunoglobulin heavy chain allele comprises a human VH gene segment, a human DH gene segment, and a human JH gene segment at an endogenous mouse heavy chain locus that comprises a human heavy chain gene that expresses a human/mouse heavy chain. In a specific embodiment, the mouse comprises two immunoglobulin heavy chain alleles, and the mouse expresses a human/mouse heavy chain.
[0066] In one embodiment, the mouse comprises a first light chain allele that comprises an unrearranged h and an unrearranged hJi , at an endogenous mouse κ locus that comprises an endogenous CK gene; and a second light chain allele that comprises an unrearranged hVX and an unrearranged hJX, at an endogenous mouse κ locus that comprises an endogenous CK gene. In a specific embodiment, the first and the second light chain alleles are the only functional light chain alleles of the genetically modified mouse. In a specific embodiment, the mouse comprises a nonfunctional λ locus. In one embodiment, the genetically modified mouse does not express a light chain that comprises a λ constant region.
[0067] In one embodiment, the mouse comprises a first light chain allele that comprises an unrearranged h and an unrearranged hJK, at an endogenous mouse κ locus that comprises an endogenous CK gene; and a second light chain allele that comprises an unrearranged hVX and an unrearranged hJX, at an endogenous mouse λ locus that comprises an endogenous CX gene. In a specific embodiment, the first and the second light chain alleles are the only functional light chain alleles of the genetically modified mouse. In one embodiment, the endogenous CX gene is CX2. In a specific embodiment, the mouse CX gene is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse CX2.
[0068] In one embodiment, the mouse comprises six immunoglobulin alleles, wherein the first allele comprises an unrearranged immunoglobulin VX and JX gene segment at an endogenous mouse κ light chain locus that comprises a mouse CK gene, the second comprises an unrearranged immunoglobulin VK and JK gene segment at an endogenous mouse κ light chain locus that comprises a mouse CK gene, the third comprises an unrearranged immunoglobulin VX and JX gene segment at an endogenous mouse λ light chain locus that comprises a mouse CX gene, the fourth and fifth each independently comprise an unrearranged VH and DH and JH gene segment at an endogenous mouse heavy chain locus that comprises a mouse heavy chain gene, and the sixth comprises either (a) an unrearranged immunoglobulin VX and JX gene segment at an endogenous mouse λ light chain locus that comprises a mouse CX gene, (b) a λ locus that is nonfunctional, or (c) a deletion in whole or in part of the λ locus.
[0069] In one embodiment, the first allele comprises an unrearranged VX and hJX. In one embodiment, the second allele comprises an unrearranged h and hJi . In one embodiment, the third allele comprises an unrearranged hX λ and hJX. In one
embodiment, the fourth and fifth each independently comprise an unrearranged hVH and hDH and hJH. In one embodiment, the sixth allele comprises an endogenous mouse λ locus that is deleted in whole or in part.
[0070] In one embodiment, the mouse comprises six immunoglobulin alleles, wherein the first allele comprises an unrearranged immunoglobulin \/λ and ϋλ gene segment at an endogenous mouse λ light chain locus that comprises a mouse CX gene, the second comprises an unrearranged immumoglobulin \/λ and ϋλ gene segment at an endogenous mouse λ light chain locus that comprises a mouse CX gene, the third comprises an unrearranged immunoglobulin V and JK gene segment at an endogenous mouse κ light chain locus that comprises a mouse CK gene, the fourth and fifth each independently comprise an unrearranged VH and DH and JH gene segment at an endogenous mouse heavy chain locus that comprises a mouse heavy chain gene, and the sixth comprises either (a) an unrearranged immunoglobulin VK and JK gene segment at an endogenous mouse K light chain locus that comprises a mouse CK gene, (b) a κ locus that is nonfunctional, or (c) a deletion of one or more elements of the κ locus.
[0071 ] In one embodiment, the first allele comprises an unrearranged hN λ and hJX gene segment. In one embodiment, the second allele comprises an unrearranged hVX and hJX gene segment. In one embodiment, the third allele comprises an unrearranged hN/κ and hJK gene segment. In one embodiment, the fourth and fifth each independently comprise an unrearranged hVH and hDH and hJH gene segment. In one embodiment, the sixth allele comprises an endogenous mouse κ locus that is functionally silenced.
[0072] In one embodiment, the genetically modified mouse comprises a B cell that comprises a rearranged antibody gene comprising a rearranged h\A. domain operably linked to a mouse CL domain. In one embodiment, the mouse CL domain is selected from a mouse CK and a mouse CX domain. In a specific embodiment, the mouse CX domain is derived from a CX2 gene. In a specific embodiment, the mouse CX domain is derived from a C domain that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse C 2.
[0073] In one aspect, a genetically modified mouse is provided that expresses a νλ region on a CL that is a CK. In one aspect, a genetically modified mouse is provided that expresses a hVX region on a CL selected from a human CK, a human C , or a mouse CK. In one aspect, a genetically modified mouse is provided that expresses a h\A. region on a mouse CK.
[0074] In one embodiment, about 10-50% of the splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 9-28% express an immunoglobulin light chain comprising a hV domain fused to a mouse CK domain.
[0075] In a specific embodiment, about 23-34% of the splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 9-1 1 % express an immunoglobulin light chain comprising a hN λ domain fused to a mouse CK domain.
[0076] In a specific embodiment, about 19-31 % of the splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 9-17% express an immunoglobulin light chain comprising a hN/λ domain fused to a mouse CK domain.
[0077] In a specific embodiment, about 21 -38% of the splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 24-27% express an immunoglobulin light chain comprising a hN λ domain fused to a mouse CK domain.
[0078] In a specific embodiment, about 10-14% of the splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 9-13% express an immunoglobulin light chain comprising a hV domain fused to a mouse CK domain.
[0079] In a specific embodiment, about 31 -48% of the splenocytes of the mouse are B cells (i.e. , CD19-positive), or which about 15-21 % express an immunoglobulin light chain comprising a hV domain fused to a mouse CK domain. In a specific embodiment, about 30-38% of the splenocytes of the mouse are B cells (i.e., CD19-positive), of which about 33-48% express an immunoglobulin light chain comprising a hVX domain fused to a mouse CK domain.
[0080] In one embodiment, about 52-70% of the bone marrow of the mouse are B cells (i.e., CD19-positive), or which about 31 -47% of the immature B cells (i.e. , CD19- positive/B220-intermediate positive/lgM-positive) express an immunoglobulin light chain comprising a h\A. domain fused to a mouse CK domain.
[0081] In one embodiment, about 60% of the bone marrow of the mouse are B cells (i.e. , CD19-positive), or which about 38.3% of the immature B cells (i.e. , CD19- positive/B220-intermediate positive/lgM-positive) express an immunoglobulin light chain comprising a hN/λ domain fused to a mouse CK domain. [0082] In one embodiment, the mouse expresses an antibody comprising a light chain that comprises a variable domain derived from a human V and a human J gene segment, and a constant domain derived from a mouse constant region gene. In one embodiment, the mouse constant region gene is a CK gene. In another embodiment, the mouse constant region gene is a CX gene. In a specific embodiment, the CX region is CX2. In a specific embodiment, the mouse CX gene is derived from a CX gene that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse CX2. In a specific embodiment, the antibody further comprises a heavy chain comprising a variable domain derived from a human V, a human D and a human J gene segment, and a heavy chain constant domain derived from a mouse heavy chain constant region gene. In one embodiment, the mouse heavy chain constant region gene comprises a hinge-CH2- CH3 sequence of a heavy chain constant domain. In another embodiment, the mouse heavy chain constant region gene comprises a CH1-hinge-CH2-CH3 sequence of a heavy chain constant domain. In another embodiment, the mouse heavy chain constant region gene comprises a CH CH2-CH3-CH4 sequence of a heavy chain constant domain. In another embodiment, the mouse heavy chain constant region gene comprises a CH2-CH3- CH4 sequence of a heavy chain constant domain.
[0083] In one embodiment, the mouse expresses an antibody comprising a light chain that comprises a rearranged human VX-JX sequence and a mouse CK sequence. In one embodiment, the rearranged human Ν/λ-ϋλ sequence is derived from a rearrangement of hX λ gene segments selected from a 3-1 , 4-3, 2-8, 3-9, 3-10, 2-14, 3-19, 2-23, 3-25, 1 -40, 7-43, 1 -44, 5-45, 7-46, 1 -47, 9-49, and a 1 -51 gene segment. In one embodiment, the rearranged human λ/λ-ϋλ sequence is derived from a rearrangement of Ιιϋλ gene segments selected from JX1 , JX2, ϋλ3, and a JX7 gene segment.
[0084] In one embodiment, the mouse expresses an antibody comprising a light chain that comprises a rearranged immunoglobulin λ light chain variable region comprising a human νλ/ϋλ sequence selected from 3-1 /1 , 3-1/7, 4-3/1 , 4-3/7, 2-8/1 , 3-9/1 , 3-10/1 , 3- 10/3, 3-10/7, 2-14/1 , 3-19/1 , 2-23/1 , 3-25/1 , 1 -40/1 , 1 -40/2, 1 -40/3, 1 -40/7, 7-43/1 , 7-43/3, 1 -44/1 , 1 -44/7, 5-45/1 , 5-45/2, 5-45/7, 7-46/1 , 7-46/2, 7-46/7, 9-49/1 , 9-49/2, 9-49/7 and 1 - 51 /1 . In a specific embodiment, the B cell expresses an antibody comprising a human immunoglobulin heavy chain variable domain fused with a mouse heavy chain constant domain, and a human immunoglobulin λ light chain variable domain fused with a mouse κ light chain constant domain.
[0085] In one aspect, a mouse is provided that expresses an antibody comprising (a) a heavy chain comprising a heavy chain variable domain derived from an unrearranged human heavy chain variable region gene segment, wherein the heavy chain variable domain is fused to a mouse heavy chain constant (CH) region; and, (b) a light chain comprising a light chain variable domain derived from an unrearranged hN λ and a Jk, wherein the light chain variable domain is fused to a mouse CL region.
[0086] In one embodiment, the mouse comprises (i) a heavy chain locus that comprises a replacement of all or substantially all functional endogenous mouse V, D and J gene segments with all or substantially all functional human V, D, and J gene segments, a mouse CH gene, (ii) a first κ light chain locus comprising a replacement of all or substantially all functional endogenous mouse VK and JK gene segments with all, substantially all, or a plurality of, functional hN λ and hJX gene segments, and a mouse CK gene, (iii) a second κ light chain locus comprising a replacement of all or substantially all functional endogenous mouse VK and JK gene segments with all, substantially all, or a plurality of, functional hN/κ and ηϋκ gene segments, and a mouse CK gene. In one embodiment, the mouse does not express an antibody that comprises a Ck region. In one embodiment, the mouse comprises a deletion of a C gene and/or a νλ and/or a ϋλ gene segment. In one embodiment, the mouse comprises a nonfunctional λ light chain locus. In a specific embodiment, the λ light chain locus is deleted in whole or in part.
[0087] In one embodiment, the mouse comprises (i) a heavy chain locus that comprises a replacement of all or substantially all functional endogenous mouse V, D and J gene segments with all or substantially all functional human V, D, and J gene segments, a mouse CH gene, (ii) a first λ light chain locus comprising a replacement of all or substantially all functional endogenous mouse Vk and Jk gene segments with all, substantially all, or a plurality of, functional hN/λ and hJk gene segments, and a mouse Ck gene, (iii) a second λ light chain locus comprising a replacement of all or substantially all functional endogenous mouse νλ and ϋλ gene segments with all, substantially all, or a plurality of, functional hN λ and hJX gene segments, and a mouse Ck gene. In a specific embodiment, the mouse Ck gene is Ck2. In a specific embodiment, the mouse Ck gene is derived from a Ck gene that is at least 60%, at least 70%, at least 80% , at least 90%, at least 95% , or at least 98% identical to mouse C 2.
[0088] In one embodiment, the mouse comprises a deletion of a CK gene and/or a VK and/or a JK gene segment. In one embodiment, the mouse comprises a nonfunctional κ light chain locus.
[0089] In one aspect, a genetically modified mouse that expresses an antibody is provided, wherein greater than 1 0%, greater than 1 5%, greater than 20%, greater than 25%, greater than 30%, greater than 35% , greater than 40%, greater than 60%, greater than 70% , greater than 80% , or greater than 90% of total IgG antibody produced by the mouse comprises a λ-derived variable domain, and wherein the mouse expresses antibodies comprising a κ-derived variable domain fused with a mouse CK region. In specific embodiments, about 15-40%, 20-40%, 25-40%, 30-40%, or 35-40% of total antibody produced by the mouse comprises a λ-derived variable domain.
[0090] In one embodiment, the λ-derived variable domain is derived from a hX λ and a hJ . In one embodiment, the λ-derived variable domain is in a light chain that comprises a mouse CK region. In a specific embodiment, the λ-derived variable region is in a light chain that comprises a mouse C region. In another specific embodiment, the Ck region is a Ολ2 region. In one embodiment, the κ-derived variable domain is derived from a hN κ and a ηϋκ, and in a specific embodiment is in a light chain that comprises a mouse CK region.
[0091] In one aspect, an isolated DNA construct is provided that comprises an upstream homology arm and a downstream homology arm, wherein the upstream and the downstream homology arms target the construct to a mouse κ locus, and the construct comprises a functional unrearranged hVX segment and a functional unrearranged hJ segment, and a selection or marker sequence.
[0092] In one aspect, an isolated DNA construct is provided, comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting a mouse λ sequence upstream of mouse \ZX2, a selection cassette flanked 5' and 3' with recombinase recognition sites, and a targeting arm for targeting a mouse λ sequence 3' of mouse ϋλ2. In one embodiment, the selection cassette is a Fifed Hyg-TK cassette. In one
embodiment, the 3' targeting arm comprises mouse CX2, JX4, C 4, and mouse enhancer 2.4.
[0093] In one aspect, an isolated DNA construct is provided, comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse λ locus 5' with respect to \ λ1 , a selection cassette flanked 5' and 3' with recombinase recognition sites, and a 3' targeting arm for targeting a mouse λ sequence 3' with respect to mouse C 1 . In one embodiment, the selection cassette is a loxed neomycin cassette. In one embodiment, the 3' targeting arm comprises the mouse λ 3' enhancer and mouse λ 3' enhancer 3.1 .
[0094] In one aspect, an isolated DNA construct is provided, comprising from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse λ locus 5' with respect to \ λ2, a selection cassette flanked 5' and 3' with recombinase recognition sites, and a 3' targeting arm for targeting a mouse λ sequence 3' with respect to mouse ϋλ2 and 5' with respect to mouse CX2. In one embodiment, the selection cassette is a Fifed hygromycin-TK cassette. In one embodiment, the 3' targeting arm comprises the mouse C 2-JX4-C 4 gene segments and mouse λ enhancer 2.4.
[0095] In one aspect, an isolated DNA construct is provided, comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse λ locus 5' with respect to \/λ2, a selection cassette flanked 5' and 3' with recombinase recognition sites, a human genomic fragment comprising a contiguous region of the human λ light chain locus from h\A.3-12 downstream to the end of hJ 1 , and a 3' targeting arm for targeting a mouse λ sequence 3' with respect to mouse ϋλ2. In one embodiment, the selection cassette is a Fifed neomycin cassette. In one embodiment, the 3' targeting arm comprises the mouse Ολ2-ϋλ4-Ολ4 gene segments and mouse λ enhancer 2.4.
[0096] In one aspect, an isolated DNA construct is provided, comprising a contiguous region of the human λ light chain locus from hV 3-12 downstream to the end of hJ 1.
[0097] In one aspect, an isolated DNA construct is provided, comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse λ locus 5' with respect to νλ2, a selection cassette flanked 5' and 3' with recombinase recognition sites and a human genomic fragment comprising a contiguous region of the human λ light chain locus from hV 3-27 downstream to the end of hV 2-8. In one embodiment, the selection cassette is a Fifed hygromycin cassette. In one embodiment, the human genomic fragment comprises a 3' targeting arm. In a specific embodiment, the 3' targeting arm comprises about 53 kb of the human λ light chain locus from hVX3-12 downstream to the end of hV 2-8.
[0098] In one aspect, an isolated DNA construct is provided, comprising a contiguous region of the human λ light chain locus from hV 3-27 downstream to the end of hV 3-12.
[0099] In one aspect, an isolated DNA construct is provided, comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse λ locus 5' with respect to \/λ2, a selection cassette flanked 5' and 3' with recombinase recognition sites, a first human genomic fragment comprising a contiguous region of the human λ light chain locus from h\A5-52 downstream to the end of h\A.1-40, a restriction enzyme site, and a second human genomic fragment comprising a contiguous region of the human λ light chain locus from h\A.3-29 downstream to the end of hVX82K. In one embodiment, the selection cassette is a Fi ed neomycin cassette. In one embodiment, the restriction enzyme site is a site for a homing endonuclease. In a specific embodiment, the homing endonuclease is Pl-Scel. In on embodiment, the second human genomic fragment is a 3' targeting arm. In a specific embodiment, the 3' targeting arm comprises about 27 kb of the human λ light chain locus from hV 3-29 downstream to the end of hV 82K. [00100] In one aspect, an isolated DNA construct is provided, comprising a contiguous region of the human λ light chain locus from hV 5-52 downstream to the end of hV 1 -40.
[00101] In one aspect, an isolated DNA construct is provided, comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse κ locus 5' with respect to the endogenous VK gene segments, two juxtaposed recombinase recognition sites, a selection cassette 3' to the juxtaposed recombinase recognition sites, and a 3' targeting arm for targeting a mouse κ sequence 5' with respect to the κ light chain variable gene segments. In one embodiment, the juxtaposed recombinase recognition sites are in opposite orientation with respect to one another. In a specific embodiment, the recombinase recognition sites are different. In another specific embodiment, the recombinase recognition sites are a loxP site and a /ox511 site. In one embodiment, the selection cassette is a neomycin cassette.
[00102] In one aspect, an isolated DNA construct is provided, comprising, from 5' to 3' with respect to the direction of transcription, a targeting arm for targeting the mouse κ locus 5' with respect to the mouse JK gene segments, a selection cassette, a recombinase recognition site 3' to the selection cassette, and a 3' targeting arm for targeting a mouse κ sequence 3' with respect to the mouse JK gene segments and 5' to the mouse κ intronic enhancer. In one embodiment, the selection cassette is a hygromycin-TK cassette. In one embodiment, the recombinase recognition site is in the same direction with respect to transcription as the selection cassette. In a specific embodiment, the recombinase recognition site is a loxP site.
[00103] In one aspect, an isolated DNA construct is provided, comprising, from 5' to 3' with respect to the direction of transcription, a first mouse genomic fragment comprising sequence 5' of the endogenous mouse VK gene segments, a first recombinase recognition site, a second recombinase recognition site, and a second mouse genomic fragment comprising sequence 3' of the endogenous mouse JK gene segments and 5' of the mouse κ intronic enhancer.
[00104] In one aspect, a genetically modified mouse is provided, wherein the genetic modification comprises a modification with one or more of the DNA constructs described above or herein.
[00105] In one aspect, use of an isolated DNA construct to make a mouse as described herein is provided. In one aspect, use of an isolated DNA construct as described herein in a method for making an antigen-binding protein is provided.
[00106] In one aspect, a non-human stem cell is provided that comprises a targeting vector that comprises a DNA construct as described above and herein. In one aspect, a non-human stem cell is provided, wherein the non-human stem cell is derived from a mouse described herein.
[00107] In one embodiment, the non-human stem cell is an embryonic stem (ES) cell. In a specific embodiment, the ES cell is a mouse ES cell.
[00108] In one aspect, use of a non-human stem cell as described herein to make a mouse as described herein is provided. In one aspect, use of a non-human stem cell as described herein to make an antigen-binding protein is provided.
[00109] In one aspect, a mouse embryo is provided, wherein the mouse embryo comprises a genetic modification as provided herein. In one embodiment, a host mouse embryo that comprises a donor ES cell is provided, wherein the donor ES cell comprises a genetic modification as described herein. In one embodiment, the mouse embryo is a pre- morula stage embryo. In a specific embodiment, the pre-morula stage embryo is a 4-cell stage embryo or an 8-cell stage embryo. In another specific embodiment, the mouse embryo is a blastocyst.
[00110] In one aspect, use of a mouse embryo as described herein to make a mouse as described herein is provided. In one aspect, use of a mouse embryo as described herein to make an antigen-binding protein is provided.
[00111] In one aspect, a non-human cell is provided, wherein the non-human cell comprises a rearranged immunoglobulin light chain gene sequence derived from a genetically modified mouse as described herein. In one embodiment, the cell is a B cell. In one embodiment, the cell is a hybridoma. In one embodiment, the cell encodes an immunoglobulin light chain variable domain and/or an immunoglobulin heavy chain variable domain that is somatically mutated.
[00112] In one aspect, a non-human cell is provided, wherein the non-human cell comprises a rearranged immunoglobulin light chain gene sequence derived from a genetically modified mouse as described herein. In one embodiment, the cell is a B cell. In one embodiment, the cell is a hybridoma. In one embodiment, the cell encodes an immunoglobulin light chain variable domain and/or an immunoglobulin heavy chain variable domain that is somatically mutated.
[00113] In one aspect, use of a non-human cell as described herein to make a mouse as described herein is provided. In one aspect, use of a non-human cell as described herein to make an antigen-binding protein is provided.
[00114] In one aspect, a mouse B cell is provided that expresses an immunoglobulin light chain that comprises (a) a variable region derived from a hX λ gene segment and a bJ gene segment; and, (b) a mouse CL gene. In one embodiment, the mouse CL gene is selected from a CK and a CX gene. In a specific embodiment, the Ck gene is C 2. In a specific embodiment, the mouse C gene is derived from a C gene that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse C 2. In one embodiment, the mouse B cell further expresses a cognate heavy chain that comprises (c) a variable region derived from a hVH, a hDH, and (d) a hJH segment. In one embodiment, the B cell does not comprise a rearranged λ gene. In another embodiment, the B cell does not comprise a rearranged κ gene.
[001 15] In one aspect, a method for making an antibody in a genetically modified mouse is provided, comprising: (a) exposing a genetically modified mouse to an antigen, wherein the mouse has a genome comprising at least one hX λ and at least one hJ at an endogenous light chain locus, wherein the endogenous light chain locus comprises a mouse CL gene; (b) allowing the genetically modified mouse to develop an immune response to the antigen; and, (c) isolating from the mouse of (b) an antibody that specifically recognizes the antigen, or isolating from the mouse of (b) a cell comprising an immunoglobulin domain that specifically recognizes the antigen, wherein the antibody comprises a light chain derived from a hN λ, a hJX and a mouse CL gene. In a specific embodiment, the mouse CL gene is a mouse CK gene.
[001 16] In one embodiment, a method for making an antibody in a genetically modified mouse is provided, comprising: (a) exposing a genetically modified mouse to an antigen, wherein the mouse has a genome comprising at least one hX λ at an endogenous κ locus and at least one hJ at the κ locus, wherein the κ locus comprises a mouse CK gene; (b) allowing the genetically modified mouse to develop an immune response to the antigen; and, (c) isolating from the mouse of (b) an antibody that specifically recognizes the antigen, or isolating from the mouse of (b) a cell comprising an immunoglobulin domain that specifically recognizes the antigen, wherein the antibody comprises a light chain derived from a hN/λ, a ηϋλ and a mouse CK gene.
[001 17] In one embodiment, the κ light chain constant gene is selected from a human CK gene and a mouse CK gene.
[001 18] In one embodiment, a method for making an antibody in a genetically modified mouse is provided, comprising: (a) exposing a genetically modified mouse to an antigen, wherein the mouse has a genome comprising at least one hN/λ at a λ light chain locus and at least one ϋλ at the λ light chain locus, wherein the λ light chain locus comprises a mouse CK gene; (b) allowing the genetically modified mouse to develop an immune response to the antigen; and, (c) isolating from the mouse of (b) an antibody that specifically recognizes the antigen, or isolating from the mouse of (b) a cell comprising an immunoglobulin domain that specifically recognizes the antigen, or identifying in the mouse of B a nucleic acid sequence encoding a heavy and/or light chain variable domain that binds the antigen, wherein the antibody comprises a light chain derived from a hN/λ, a hJ and a mouse Ck gene.
[001 19] In one embodiment, the λ light chain constant gene is selected from a human CK gene and a mouse Ck gene. In one embodiment, the λ light chain constant gene is a human Ck gene. In a specific embodiment, the human Ck gene is selected from Ολ1 , Ck2, Ck3 and Ckl. In one embodiment, the λ light chain constant gene is a mouse Ck gene. In a specific embodiment, the mouse Ck gene is selected from C 1 , Ckl and CK2>. In a more specific embodiment, the mouse Ck gene is Ckl. In another specific embodiment, the mouse Ck gene is derived from a Ck gene that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse Ckl.
[00120] In one aspect, a method for making a rearranged antibody gene in a genetically modified mouse is provided, comprising: (a) exposing a genetically modified mouse to an antigen, wherein the genetic modification comprises a YNK and a hJ at an endogenous light chain locus, wherein the endogenous light chain locus comprises a mouse CL gene or functional fragment thereof; and, (b) identifying a rearranged immunoglobulin gene in said mouse, wherein the rearranged immunoglobulin gene comprises a λ light chain variable region gene segment and a CL gene or functional fragment thereof.
[00121] In one embodiment, the method further comprises cloning a nucleic acid sequence encoding a heavy and/or light chain variable region from the mouse, wherein the heavy and/or light chain variable region is from an antibody that comprises a human k and a mouse CL.
[00122] In one embodiment, the mouse CL gene or functional fragment thereof is selected from a human CL gene and a mouse CL gene, or functional fragment thereof.
[00123] In one embodiment, a method for making a rearranged antibody gene in a genetically modified mouse is provided, comprising: (a) exposing a genetically modified mouse to an antigen, wherein the genetic modification comprises a Vk and a hJk at a κ light chain locus, wherein the κ light chain locus comprises a mouse CK gene or functional fragment thereof; and, (b) identifying a rearranged immunoglobulin gene in said mouse, wherein the rearranged immunoglobulin gene comprises a λ light chain variable region gene segment and a CK gene or functional fragment thereof.
[00124] In one embodiment, the κ light chain constant gene or functional fragment thereof is selected from a human CK gene and a mouse CK gene, or a functional fragment thereof.
[00125] In one embodiment, the method further comprises cloning a nucleic acid sequence encoding a heavy and/or light chain variable region from the mouse, wherein the heavy and/or light chain variable region is from an antibody that comprises a human VX and a mouse CK,
[00126] In one embodiment, a method for making a rearranged antibody gene in a genetically modified mouse is provided, comprising: (a) exposing a genetically modified mouse to an antigen, wherein the genetic modification comprises a hVX and a hJX at a mouse λ light chain locus, wherein the λ light chain locus comprises a mouse CX gene or functional fragment thereof; and, (b) identifying a rearranged immunoglobulin gene in said mouse, wherein the rearranged immunoglobulin gene comprises a λ light chain variable region gene segment and a CX gene or functional fragment thereof.
[001 27] In one embodiment, the λ light chain constant gene or functional fragment thereof is selected from a human CX gene and a mouse CX gene, or a functional fragment thereof. In a specific embodiment, the λ light chain constant gene is a mouse CX gene, or a functional fragment thereof.
[00128] In one embodiment, the method further comprises cloning a nucleic acid sequence encoding a heavy and/or light chain variable region from the mouse, wherein the heavy and/or light chain variable region is from an antibody that comprises a human VX and a mouse CX.
[00129] In one aspect, a method for making an antibody is provided, comprising exposing a mouse as described herein to an antigen, allowing the mouse to mount an immune response that comprises making an antibody that specifically binds the antigen, identifying a rearranged nucleic acid sequence in the mouse that encodes heavy chain and a rearranged nucleic acid sequence in the mouse that encodes a cognate light chain variable domain sequence of an antibody, wherein the antibody specifically binds the antigen, and employing the nucleic acid sequences of the heavy and light chain variable domains fused to human constant domains to make a desired antibody, wherein the desired antibody comprises a light chain that comprises a VX domain fused to a CL domain. In one embodiment, the VX domain is human and the CL domain is a human or mouse CX domain. In one embodiment, the VX domain is mouse and the CL domain is a human or mouse CK domain.
[001 30] In one embodiment, a method for making an antibody is provided, comprising exposing a mouse as described herein to an antigen, allowing the mouse to mount an immune response that comprises making an antibody that specifically binds the antigen, identifying a rearranged nucleic acid sequence in the mouse that encodes a heavy chain and a rearranged nucleic acid sequence in the mouse that encodes a cognate light chain variable domain sequence of an antibody, wherein the antibody specifically binds the antigen, and employing the nucleic acid sequences of the heavy and light chain variable domains fused to nucleic acid sequences of human constant domains to make a desired antibody, wherein the desired antibody comprises a light chain that comprises a \/λ domain fused to a CK domain.
[00131] In one embodiment, a method for making an antibody is provided, comprising exposing a mouse as described herein to an antigen, allowing the mouse to mount an immune response that comprises making an antibody that specifically binds the antigen, identifying a rearranged nucleic acid sequence in the mouse that encodes a heavy chain variable domain and a rearranged nucleic acid sequence that encodes a cognate light chain variable domain sequence of an antibody, wherein the antibody specifically binds the antigen, and employing the nucleic acid sequences fused to nucleic acid sequences that encode a human heavy chain constant domain and a human light chain constant domain to make an antibody derived from human sequences, wherein the antibody that specifically binds the antigen comprises a light chain that comprises a human νλ domain fused to a mouse CX region.
[00132] In one embodiment, the mouse C region is selected from Ολ1 , Ολ2 and Ολ3. In a specific embodiment, the mouse Ck region is Ολ2.
[00133] In one aspect, a method for making a rearranged antibody light chain variable region gene sequence is provided, comprising (a) exposing a mouse as described herein to an antigen; (b) allowing the mouse to mount an immune response; (c) identifying a cell in the mouse that comprises a nucleic acid sequence that encodes a rearranged human \/λ domain sequence fused with a mouse CL domain, wherein the cell also encodes a cognate heavy chain comprising a human VH domain and a mouse CH domain, and wherein the cell expresses an antibody that binds the antigen; (d) cloning from the cell a nucleic acid sequence encoding the human νλ domain and a nucleic acid sequence encoding the cognate human VH domain; and, (e) using the cloned nucleic acid sequence encoding the human \/k domain and the cloned nucleic acid sequence encoding the cognate human VH domain to make a fully human antibody.
[00134] !n one embodiment, a method for making a rearranged antibody light chain variable region gene sequence is provided, comprising (a) exposing a mouse as described in this disclosure to an antigen; (b) allowing the mouse to mount an immune response; (c) identifying a cell in the mouse that comprises a nucleic acid sequence that encodes a rearranged human \/λ domain sequence contiguous on the same nucleic acid molecule with a nucleic acid sequence encoding a mouse CK domain, wherein the cell also encodes a cognate heavy chain comprising a human VH domain and a mouse CH domain, and wherein the cell expresses an antibody that binds the antigen; (d) cloning from the cell a nucleic acids sequence encoding the human \/λ domain and a nucleic acid sequence encoding the cognate human VH domain; and, (e) using the cloned nucleic acid sequence encoding the human VX domain and the cloned nucleic acid sequence encoding the cognate human VH domain to make a fully human antibody.
[00135] In one embodiment, a method for making a rearranged antibody light chain variable region gene sequence is provided, comprising (a) exposing a mouse as described herein to an antigen; (b) allowing the mouse to mount an immune response to the antigen; (c) identifying a cell in the mouse that comprises DNA that encodes a rearranged human \/λ domain sequence fused with a mouse CX domain, wherein the cell also encodes a cognate heavy chain comprising a human VH domain and a mouse CH domain, and wherein the cell expresses an antibody that binds the antigen; (d) cloning from the cell a nucleic acid sequence encoding the rearranged human VX domain and a nucleic acid sequence encoding the cognate human VH domain; and, (e) using the cloned nucleic acid sequence encoding the human VX domain and the cloned nucleic acid sequence encoding the cognate human VH domain to make a fully human antibody. In one embodiment, the mouse CX domain is mouse CX2. In a specific embodiment, the mouse CX domain is derived from a CX gene that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse CX2.
[001 36] In one aspect, a genetically modified mouse is provided that expresses a human λ-derived light chain fused to an endogenous light chain constant region (CL), wherein the mouse, upon immunization with antigen, makes an antibody comprising a human VX domain fused to a mouse CL domain. In one embodiment, the mouse CL domain is selected from a CK domain and a CX domain. In one embodiment, the mouse CL domain is a CK domain. In one embodiment, the mouse CL domain is a CX domain. In a specific embodiment, the CX domain is CX2. In a specific embodiment, the mouse CX domain is derived from a CX gene that is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 98% identical to mouse CX2.
[001 37] In one aspect, a genetically modified mouse comprising a modified endogenous K or X light chain locus as described herein, is provided that expresses a plurality of immunoglobulin X light chains associated with a plurality of immunoglobulin heavy chains. In one embodiment, the heavy chain comprises a human sequence. In various
embodiments, the human sequence is selected from a variable sequence, a CH1 , a hinge, a CH2, a CH3, and a combination thereof. In one embodiment, the plurality of
immunoglobulin X light chains comprises a human sequence. In various embodiments, the human sequence is selected from a variable sequence, a constant sequence, and a combination thereof. In one embodiment, the mouse comprises a disabled endogenous immunoglobulin locus and expresses the heavy chain and/or the X light chain from a transgene or extrachromosomal episome. In one embodiment, the mouse comprises a replacement at an endogenous mouse locus of some or all endogenous mouse heavy chain gene segments (i.e., V, D, J), and/or some or all endogenous mouse heavy chain constant sequences (e.g., CH1 , hinge, CH2, CH3, or a combination thereof), and/or some or all endogenous mouse light chain sequences (e.g., V, J, constant, or a combination thereof), with one or more human immunoglobulin sequences.
[00138] In one aspect, a mouse suitable for making antibodies that have a human λ- derived light chain is provided, wherein all or substantially all antibodies made in the mouse are expressed with a human λ-derived light chain. In one embodiment, the human λ-derived light chain is expressed from an endogenous light chain locus. In one embodiment, the endogenous light chain locus is a κ light chain locus. In a specific embodiment, the κ light chain locus is a mouse κ light chain locus.
[00139] In one aspect, a method for making a λ-derived light chain for a human antibody is provided, comprising obtaining from a mouse as described herein a light chain sequence and a heavy chain sequence, and employing the light chain sequence and the heavy chain sequence in making a human antibody.
[00140] In one aspect, a method for making an antigen-binding protein is provided, comprising exposing a mouse as described herein to an antigen; allowing the mouse to mount an immune response; and obtaining from the mouse an antigen-binding protein that binds the antigen, or obtaining from the mouse a sequence to be employed in making an antigen-binding protein that binds the antigen.
[00141] In one aspect, a cell derived from a mouse as described herein is provided. In one embodiment, the cell is selected from an embryonic stem cell, a pluripotent cell, an induced pluripotent cell, a B cell, and a hybridoma.
[00142] In one aspect, a cell is provided that comprises a genetic modification as described herein. In one embodiment, the cell is a mouse cell. In one embodiment, the cell is selected from a hybridoma and a quadroma. In one embodiment, the cell expresses an immunoglobulin light chain that comprises a human λ variable sequence fused with a mouse constant sequence. In a specific embodiment, the mouse constant sequence is a mouse K constant sequence.
[00143] In one aspect, a tissue derived from a mouse as described herein is provided.
[00144] In one aspect, use of a mouse or a cell as described herein to make an antigen- binding protein is provided. In one embodiment, the antigen-binding protein is a human protein. In one embodiment, the human protein is a human antibody. [00145] In one aspect, an antigen-binding protein made by a mouse, cell, tissue, or method as described herein is provided. In one embodiment, the antigen-binding protein is a human protein. In one embodiment, the human protein is a human antibody.
[00146] Any of the embodiments and aspects described herein can be used in conjunction with one another, unless otherwise indicated or apparent from the context. Other embodiments will become apparent to those skilled in the art from a review of the ensuing description.
BRIEF DESCRIPTION OF THE FIGURES
[00147] FIG. 1 shows a detailed illustration, not to scale, of the human λ light chain locus including the clusters of \ λ gene segments (A, B and C) and the ϋλ and C region pairs (J-C pairs)
[00148] FIG. 2 shows a general illustration, not to scale, of a targeting strategy used to inactivate the endogenous mouse λ light chain locus.
[00149] FIG. 3 shows a general illustration, not to scale, of a targeting strategy used to inactivate the endogenous mouse κ light chain locus.
[00150] FIG. 4A shows a general illustration, not to scale of an initial targeting vector for targeting the endogenous mouse λ light chain locus with human λ light chain sequences including 12 hV gene segments and hJX1 gene segment (12/1-λ Targeting Vector).
[00151] FIG. 4B shows a general illustration, not to scale, of four initial targeting vectors for targeting the endogenous mouse κ light chain locus with human λ light chain sequences including 12 hN λ gene segments and hJ 1 gene segment (12/1-κ Targeting Vector), 12 hA/λ gene segments and hJ 1 , 2, 3 and 7 gene segments (12/4-κ Targeting Vector), 12 hV gene segments, a human V -JK genomic sequence and Ιιϋλ1 gene segment (12(κ)1-κ Targeting Vector) and 12 hV gene segments, a human VK-JK genomic sequence and hJ 1 , 2, 3 and 7 gene segments (12(κ)4-κ Targeting Vector).
[00152] FIG. 5A shows a general illustration, not to scale, of a targeting strategy for progressive insertion of 40 hVX gene segments and a single J gene segment into the mouse λ light chain locus.
[00153] FIG. 5B shows a general illustration, not to scale, of a targeting strategy for progressive insertion of 40 hVX gene segments and a single hJ gene segment into the mouse K locus.
[00154] FIG. 6 show a general illustration, not to scale, of the targeting and molecular engineering steps employed to make unique human λ-κ hybrid targeting vectors for construction of a hybrid light chain locus containing a human κ intergenic sequence, multiple J gene segments or both. [001 55] FIG. 7A shows a general illustration, not to scale, of the locus structure for a modified mouse λ light chain locus containing 40 hV gene segments and a single bJk gene segment operably linked to the endogenous Ck2 gene.
[00156] FIG. 7B shows a general illustration, not to scale, of the locus structure for four independent, modified mouse κ light chain loci containing 40 hN λ gene segments and either one or four bJk gene segments with or without a contiguous human VK-JK genomic sequence operably linked to the endogenous CK gene.
[001 57] FIG. 8A shows contour plots of lg + and lgK+ splenocytes gated on CD19+ from a wild type mouse (WT), a mouse homozygous for 12 hV and four bJk gene segments including a human VK-JK genomic sequence (12hV -VKjK-4hJ ) and a mouse
homozygous for 40 hV and one bJk gene segment (40hVX-1 hJ ).
[001 58] FIG. 8B shows the total number of CD19+ B cells in harvested spleens from wild type (WT), mice homozygous for 12 hV and four bJk gene segments including a human VK-JK genomic sequence (12hV -VKjK-4hJ ) and mice homozygous for 40 hV and one bJk gene segment (40hVX-1 hJ ).
[001 59] FIG. 9A, in the top panel, shows contour plots of splenocytes gated on singlets and stained for B and T cells (CD19+ and CD3+, respectively) from a wild type mouse (WT) and a mouse homozygous for 40 hV and four Jk gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJ ). The bottom panel shows contour plots of splenocytes gated on CD19+ and stained for \gk+ and lgK+ expression from a wild type mouse (WT) and a mouse homozygous for 40 hV and four Jk gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJ ).
[00160] FIG. 9B shows the total number of CD19+, CD19+!gK + and CD19+lg + B cells in harvested spleens from wild type mice (WT) and mice homozygous for 40 bVk and four Jk gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJ ).
[00161] FIG. 9C shows contour plots of splenocytes gated on CD19+ and stained for immunoglobulin D (IgD) and immunoglobulin M (IgM) from a wild type mouse (WT) and a mouse homozygous for 40 hVX and four JX gene segments including a human VK-JK genomic sequence (40hVX-VKjK-4hJ ). Mature (72 for WT, 51 for 40hV -VKjK-4h ϋλ) and transitional (13 for WT, 22 for 40hVX-VKjK-4hJ ) B cells are noted on each of the contour plots.
[00162] FIG. 9D shows the total number of CD19+ B cells, transitional B cells
(CD19+lgMhilgD'°) and mature B cells (CD19+lgMlolgDhi) in harvested spleens from wild type mice (WT) and mice homozygous for 40 hV and four JX gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJ ). [00163] FIG. 10A, in the top panel, shows contour plots of bone marrow stained for B and T cells (CD19+ and CD3+, respectively) from a wild type mouse (WT) and a mouse homozygous for 40 hN λ and four ϋλ gene segments including a human VK-JK genomic sequence (401ινλ-νκϋκ-4ηϋλ). The bottom panel shows contour plots of bone marrow gated on CD19+ and stained for ckit+ and CD43+ from a wild type mouse (WT) and a mouse homozygous for 40 hN λ and four λ gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJ ). Pro and Pre B cells are noted on the contour plots of the bottom panel.
[00164] FIG. 10B shows the number of Pro (CD19+CD43+ckit+) and Pre (CD19+CD43~ ckir) B cells in bone marrow harvested from the femurs of wild type mice (WT) and mice homozygous for 40 hN λ and four ϋλ gene segments including a human VK-JK genomic sequence (40 A -VKjK-4hJX).
[00165] FIG. 10C shows contour plots of bone marrow gated on singlets stained for immunoglobulin M (IgM) and B220 from a wild type mouse (WT) and a mouse
homozygous for 40 hV and four Jk gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJ ). Immature, mature and pro/pre B cells are noted on each of the contour plots.
[001 66] FIG. 10D shows the total number of immature (B220intlgM+) and mature (B220hllgM+) B cells in bone marrow isolated from the femurs of wild type mice (WT) and mice homozygous for 40 Ιινλ and four J gene segments including a human VK-JK genomic sequence
Figure imgf000029_0001
[001 67] FIG. 10E shows contour plots of bone marrow gated on immature (B220intlgM+) and mature (B220h,lgM+) B cells stained for and IgK expression isolated from the femurs of a wild type mouse (WT) and a mouse homozygous for 40 hV and four Jλ gene segments including a human VK-JK genomic sequence (40hV -VKjK-4hJX).
[00168] FIG. 1 1 shows a nucleotide sequence alignment of the V -J -CK junction of eighteen independent RT-PCR clones amplified from splenocyte RNA of mice bearing human λ light chain gene sequences at an endogenous mouse κ light chain locus. A6 = SEQ ID NO:57; B6 = SEQ ID NO:58; F6 = SEQ ID NO:59; B7 = SEQ ID NO:60; E7 = SEQ ID NO:61 ; F7 = SEQ ID NO:62; C8 = SEQ ID NO:63; E12 = SEQ ID NO:64; 1 -4 = SEQ ID NO:65; 1 -20 = SEQ ID NO:66; 3B43 = SEQ ID NO:67; 5-8 = SEQ ID NO:68; 5-19 = SEQ ID NO:69; 1010 = SEQ ID NO:70; 1 1A1 = SEQ ID NO:71 ; 7A8 = SEQ ID NO:72; 3A3 = SEQ ID NO:73; 2-7 = SEQ ID NO:74. Lower case bases indicate non-germline bases resulting from either mutation and/or N addition during recombination. Consensus amino acids within the Framework 4 region (FWR4) encoded by the nucleotide sequence of hJkl and mouse CK are noted at the bottom of the sequence alignment. [00169] FIG. 12 shows a nucleotide sequence alignment of the Ν/λ-ϋλ-Οκ junction of twelve independent RT-PCR clones amplified from splenocyte RNA of mice bearing human λ light chain gene sequences including a contiguous human VK-JK genomic sequence at an endogenous mouse κ light chain locus. 5-2 = SEQ ID NO:87; 2-5 = SEQ ID NO:88; 1-3 = SEQ ID NO:89; 4B-1 = SEQ ID NO:90; 3B-5 = SEQ ID NO:91 ; 7A-1 = SEQ ID NO:92; 5- 1 = SEQ ID NO:93; 4A-1 = SEQ ID NO:94; 1 1A-1 = SEQ ID NO:95; 5-7 = SEQ ID NO:96; 5-4 = SEQ ID NO:97; 2-3 = SEQ ID NO:98. Lower case bases indicate non-germline bases resulting from either mutation and/or N addition during recombination. Consensus amino acids within the Framework 4 region (FWR4) encoded by the nucleotide sequence of each human ϋλ and mouse C are noted at the bottom of the sequence alignment.
[00170] FIG. 13 shows a nucleotide sequence alignment of the Ν λ-ϋλ-ΰλ junction of three independent RT-PCR clones amplified from splenocyte RNA of mice bearing human λ light chain gene sequences at an endogenous mouse λ light chain locus. 2D1 = SEQ ID NO:101 ; 2D9 = SEQ ID NO:102; 3E15 = SEQ ID NO:103. Lower case bases indicate non-germline bases resulting from either mutation and/or N addition during recombination. Consensus amino acids within the Framework 4 region (FWR4) encoded by the nucleotide sequence of hJ 1 and mouse C 2 are noted at the bottom of the sequence alignment.
DETAILED DESCRIPTION
[00171 ] Although specific features of various embodiments are discussed in detail, the descriptions of the specific aspects, embodiments, and examples do not limit the subject matter of the claims; it is the claims that describe the scope of the invention. All terms and phrases used in this disclosure include the meanings normally ascribed to them in the art.
[00172] The term "contiguous" includes reference to occurrence on the same nucleic acid molecule, e.g., two nucleic acid sequences are "contiguous" if they occur on the same nucleic molecule but are interrupted by another nucleic acid sequence. For example, a rearranged V(D)J sequence is "contiguous" with a constant region gene sequence, although the final codon of the V(D)J sequence is not followed immediately by the first codon of the constant region sequence. In another example, two V gene segment sequences are "contiguous" if they occur on the same genomic fragment, although they may be separated by sequence that does not encode a codon of the V region, e.g. , they may be separated by a regulatory sequence, e.g., a promoter or other noncoding sequence. In one embodiment, a contiguous sequence includes a genomic fragment that contains genomic sequences arranged as found in a wild-type genome.
[00173] The phrase "derived from" when used concerning a variable region "derived from" a cited gene or gene segment includes the ability to trace the sequence back to a particular unrearranged gene segment or gene segments that were rearranged to form a gene that expresses the variable domain (accounting for, where applicable, splice differences and somatic mutations).
[00174] The phrase "functional" when used concerning a variable region gene segment or joining gene segment refers to usage in an expressed antibody repertoire; e.g. , in humans νλ gene segments 3-1 , 4-3, 2-8, etc. are functional, whereas νλ gene segments 3-2, 3-4, 2-5, etc. are nonfunctional.
[00175] A "heavy chain locus" includes a location on a chromosome, e.g., a mouse chromosome, wherein in a wild-type mouse heavy chain variable (VH) , heavy chain diversity (DH), heavy chain joining (JH), and heavy chain constant (CH) region DNA sequences are found.
[00176] A "K locus" includes a location on a chromosome, e.g., a mouse chromosome, wherein in a wild-type mouse Kvariable (VK), K joining (JK), and κ constant (CK) region DNA sequences are found.
[00177] A "λ locus" includes a location on a chromosome, e.g., a mouse chromosome, wherein in a wild-type mouse λ variable (VX), λ joining (ϋλ), and λ constant (C ) region DNA sequences are found.
[00178] The term "unrearranged" includes the state of an immunoglobulin locus wherein V gene segments and J gene segments (for heavy chains, D gene segments as well) are maintained separately but are capable of being joined to form a rearranged V(D)J gene that comprises a single V,(D),J of the V(D)J repertoire.
Mice Expressing Human λ Variable Domains
[00179] Mice that express antibodies that are fully human, or partly human and partly mouse, have previously been reported. VELOCIMMUNE® genetically engineered mice comprise a replacement of unrearranged V(D)J gene segments at endogenous mouse loci with human V(D)J gene segments. VELOCIMMUNE® mice express chimeric antibodies having human variable domains and mouse constant domains (see, e.g., US Pat. No. 7,605,237). Most other reports concern mice that express fully human antibodies from fully human transgenes in mice that have disabled endogenous immunoglobulin loci.
[00180] Antibody light chains are encoded by one of two separate loci: kappa (κ) and lambda (λ). Mouse antibody light chains are primarily of the κ type. Mice that make mouse antibodies, and modified mice that make fully human or chimeric human-mouse antibodies, display a bias in light chain usage. Humans also exhibit light chain bias, but not so pronounced as in mice; the ratio of κ light chains to λ light chains in mice is about 95:5, whereas in humans the ratio is about 60:40. The more pronounced bias in mice is not thought to severely affect antibody diversity, because in mice the λ variable locus is not so diverse in the first instance. This is not so in humans. The human λ light chain locus is richly diverse.
[00181] The human λ light chain locus extends over 1 ,000 kb and contains over 80 genes that encode variable (V) or joining (J) segments (FIG. 1 ). Within the human λ light chain locus, over half of all observed νλ domains are encoded by the gene segments 1 -40, 1 -44, 2-8, 2-14, and 3-21 . Overall, about 30 or so of the human \/λ gene segments are believed to be functional. There are seven ϋλ gene segments, only four of which are regarded as generally functional ϋλ gene segments— ϋλ1 , ϋλ2, ϋλ3, and ϋλ7.
[00182] The λ light chain locus in humans is similar in structure to the κ locus of both mice and humans in that the human λ light chain locus has several variable region gene segments that are capable of recombining to form a functional light chain protein. The human λ light chain locus contains approximately 70 V gene segments and 7 ϋλ-Ολ gene segment pairs. Only four of these ϋλ-Ολ gene segment pairs appear to be functional. In some alleles, a fifth ϋλ-Ολ gene segment pair is reportedly a pseudo gene (Ολ6). The 70 \/λ gene segments appear to contain 38 functional gene segments. The 70 \/λ sequences are arranged in three clusters, all of which contain different members of distinct V gene family groups (clusters A, B and C; FIG. 1 ). This is a potentially rich source of relatively untapped diversity for generating antibodies with human V regions in non-human animals.
[00183] In stark contrast, the mouse λ light chain locus contains only two or three (depending on the strain) mouse V region gene segments (FIG. 2). At least for this reason, the severe κ bias in mice is not thought to be particularly detrimental to total antibody diversity.
[00184] According published maps of the mouse λ light chain locus, the locus consists essentially of two clusters of gene segments within a span of approximately 200 kb (FIG.2). The two clusters contain two sets of V, J, and C genes that are capable of independent rearrangement: Ν/λ2-ϋλ2-Ολ2-ϋλ4-Ολ4 and νλ1 -ϋλ3-Ολ3-ϋλ1 -Ολ1 . Although V 2 has been found to recombine with all ϋλ gene segments, νλ1 appears to exclusively recombine with C 1 . CX4 is believed to be a pseudo gene with defective splice sites.
[00185] The mouse κ light chain locus is strikingly different. The structure and number of gene segments that participate in the recombination events leading to a functional light chain protein from the mouse κ locus is much more complex (FIG. 3). Thus, mouse λ light chains do not greatly contribute to the diversity of an antibody population in a typical mouse. [00186] Exploiting the rich diversity of the human λ light chain locus in mice would likely result in, among other things, a source for a more complete human repertoire of light chain V domains. Previous attempts to tap this diversity used human transgenes containing chunks of the human λ light chain locus randomly incorporated into the mouse genome (see, e.g., US 6,998,514 and US 7,435,871 ). Mice containing these randomly integrated transgenes reportedly express fully human λ light chains, however, in some cases, one or both endogenous light chain loci remain intact. This situation is not desirable as the human λ light chain sequences contend with the mouse light chain (κ or λ) in the expressed antibody repertoire of the mouse.
[00187] In contrast, the inventors describe genetically modified mice that are capable of expressing one or more λ light chain nucleic acid sequences directly from a mouse light chain locus, including by replacement at an endogenous mouse light chain locus.
Genetically modified mice capable of expressing human λ light chain sequences from an endogenous locus may be further bred to mice that comprise a human heavy chain locus and thus be used to express antibodies comprising V regions (heavy and light) that are fully human. In various embodiments. The V regions express with mouse constant regions. In various embodiments, no endogenous mouse immunoglobulin gene segments are present and the V regions express with human constant regions. These antibodies would prove useful in numerous applications, both diagnostic as well as therapeutic.
[00188] Many advantages can be realized for various embodiments of expressing binding proteins derived from human \/k and ϋλ gene segments in mice. Advantages can be realized by placing human λ sequences at an endogenous light chain locus, for example, the mouse κ or λ locus. Antibodies made from such mice can have light chains that comprise human Vk domains fused to a mouse CL region, specifically a mouse CK or Ck region. The mice will also express human \/λ domains that are suitable for
identification and cloning for use with human CL regions, specifically CK and/or Ck regions. Because B cell development in such mice is otherwise normal, it is possible to generate compatible \/λ domains (including somatically mutated \/λ domains) in the context of either Ck or CK regions.
[00189] Genetically modified mice are described that comprise an unrearranged \/λ gene segment at an immunoglobulin κ or λ light chain locus. Mice that express antibodies that comprise a light chain having a human \/λ domain fused to a CK and/or Ck region are described. Sterile Transcripts of the Immunoglobulin Light Chain Locus
[00190] Variations on the theme of expressing human immunoglobulin λ sequences in mice are reflected in various embodiments of genetically modified mice capable of such expression. Thus, in some embodiments, the genetically modified mice comprise certain non-coding sequence(s) from a human locus. In one embodiment, the genetically modified mouse comprises human νλ and ϋλ gene segments at an endogenous κ light chain locus, and further comprises a human κ light chain genomic fragment. In a specific embodiment, the human κ light chain genomic fragment is a non-coding sequence naturally found between a human VK gene segment and a human JK gene segment.
[00191] The human and mouse κ light chain loci contain sequences that encode sterile transcripts that lack either a start codon or an open reading frame, and that are regarded as elements that regulate transcription of the κ light chain loci. These sterile transcripts arise from an intergenic sequence located downstream or 3' of the most proximal VK gene segment and upstream or 5' of the κ light chain intronic enhancer (Εκϊ) that is upstream of the K light chain constant region gene (CK). The sterile transcripts arise from
rearrangement of the intergenic sequence to form a VKJKI segment fused to a CK.
[00192] A replacement of the κ light chain locus upstream of the CK gene would remove the intergenic region encoding the sterile transcripts. Therefore, in various embodiments, a replacement of mouse κ light chain sequence upstream of the mouse CK gene with human λ light chain gene segments would result in a humanized mouse κ light chain locus that contains human νλ and ϋλ gene segments but not the κ light chain intergenic region that encodes the sterile transcripts.
[00193] As described herein, humanization of the endogenous mouse κ light chain locus with human λ light chain gene segments, wherein the humanization removes the intergenic region, results in a striking drop in usage of the κ light chain locus, coupled with a marked increase in λ light chain usage. Therefore, although a humanized mouse that lacks the intergenic region is useful in that it can make antibodies with human light chain variable domains (e.g., human λ or κ domains), usage from the locus decreases.
[00194] Also described is humanization of the endogenous mouse κ light chain locus with human νλ and ϋλ gene segments coupled with an insertion of a human κ intergenic region to create a V locus that contains, with respect to transcription, between the final human νλ gene segment and the first human ϋλ gene segment, a κ intergenic region; which exhibits a B cell population with a higher expression than a locus that lacks the κ intergenic region. This observation is consistent with a hypothesis that the intergenic region— directly through a sterile transcript, or indirectly— suppresses usage from the endogenous λ light chain locus. Under such a hypothesis, including the intergenic region would result in a decrease in usage of the endogenous λ light chain locus, leaving the mouse a restricted choice but to employ the modified (λ into κ) locus to generate antibodies.
[00195] In various embodiments, a replacement of mouse κ light chain sequence upstream of the mouse CK gene with human λ light chain sequence further comprises a human κ light chain intergenic region disposed, with respect to transcription, between the 3' untranslated region of the 3' most \/λ gene segment and 5' to the first human JX gene segment. Alternatively, such an intergenic region may be omitted from a replaced endogenous κ light chain locus (upstream of the mouse CK gene) by making a deletion in the endogenous λ light chain locus. Likewise, under this embodiment, the mouse generates antibodies from an endogenous κ light chain locus containing human λ light chain sequences.
Approaches to Engineering Mice to Express Human VX Domains
[00196] Various approaches to making genetically modified mice that make antibodies that contain a light chain that has a human \/λ domain fused to an endogenous CL (e.g. CK or CX) region are described. Genetic modifications are described that, in various embodiments, comprise a deletion of one or both endogenous light chain loci. For example, to eliminate mouse λ light chains from the endogenous antibody repertoire a deletion of a first VX-JX-CX gene cluster and replacement, in whole or in part, of the VX-JX gene segments of a second gene cluster with human VX-JX gene segments can be made. Genetically modified mouse embryos, cells, and targeting constructs for making the mice, mouse embryos, and cells are also provided.
[00197] The deletion of one endogenous VX-JX-CX gene cluster and replacement of the Χ λ-ϋλ gene segments of another endogenous VX-JX-CX gene cluster employs a relatively minimal disruption in natural antibody constant region association and function in the animal, in various embodiments, because endogenous CX genes are left intact and therefore retain normal functionality and capability to associate with the constant region of an endogenous heavy chain. Thus, in such embodiments the modification does not affect other endogenous heavy chain constant regions dependent upon functional light chain constant regions for assembly of a functional antibody molecule containing two heavy chains and two light chains. Further, in various embodiments the modification does not affect the assembly of a functional membrane-bound antibody molecule involving an endogenous heavy chain and a light chain, e.g., a hVX domain linked to a mouse CX region. Because at least one functional CX gene is retained at the endogenous locus, animals containing a replacement of the Ν λ-ϋλ gene segments of an endogenous Ν/λ-ϋλ- CX gene cluster with human Ν λ-ϋλ gene segments should be able to make normal λ light chains that are capable of binding antigen during an immune response through the human Ν/λ-ϋλ gene segments present in the expressed antibody repertoire of the animal.
[00198] A schematic illustration (not to scale) of a deleted endogenous mouse Ν/λ-ϋλ-Ολ gene cluster is provided in FIG. 2. As illustrated, the mouse λ light chain locus is organized into two gene clusters, both of which contain function gene segments capable of recombining to form a function mouse λ light chain. The endogenous mouse νλ1-ϋλ3-Ολ3- J 1 -C 1 gene cluster is deleted by a targeting construct (Targeting Vector 1 ) with a neomycin cassette flanked by recombination sites. The other endogenous gene cluster (V 2-VX3-J 2-C 2-JX4-C 4) is deleted in part by a targeting construct (Targeting Vector 2) with a hygromycin-thymidine kinase cassette flanked by recombination sites. In this second targeting event, the Ολ2-ϋλ4-Ολ4 endogenous gene segments are retained. The second targeting construct (Targeting Vector 2) is constructed using recombination sites that are different than those in the first targeting construct (Targeting Vector 1 ) thereby allowing for the selective deletion of the selection cassette after a successful targeting has been achieved. The resulting double-targeted locus is functionally silenced in that no endogenous λ light chain can be produced. This modified locus can be used for the insertion of human νλ and ϋλ gene segments to create an endogenous mouse λ locus comprising human VX and ϋλ gene segments, whereby, upon recombination at the modified locus, the animal produces λ light chains comprising rearranged human V and ϋλ gene segments linked to an endogenous mouse CX gene segment.
[001 99] Genetically modifying a mouse to render endogenous λ gene segments nonfunctional, in various embodiments, results in a mouse that exhibits exclusively κ light chains in its antibody repertoire, making the mouse useful for evaluating the role of λ light chains in the immune response, and useful for making an antibody repertoire comprising VK domains but not V domains.
[00200] A genetically modified mouse that expresses a hVX linked to a mouse CX gene having been recombined at the endogenous mouse λ light chain locus can be made by any method known in the art. A schematic illustration (not to scale) of the replacement of the endogenous mouse νλ2Λ λ3-ϋλ2 gene segments with human V and ϋλ gene segments is provided in FIG. 4A. As illustrated, an endogenous mouse λ light chain locus that had been rendered nonfunctional is replaced by a targeting construct (12/1-λ Targeting Vector) that includes a neomycin cassette flanked by recombination sites. The νλ2Λ λ3-ϋλ2 gene segments are replaced with a genomic fragment containing human λ sequence that includes 12 hN/λ gene segments and a single hJk gene segment.
[00201] Thus, this first approach positions one or more hN λ gene segments at the endogenous λ light chain locus contiguous with a single ηϋλ gene segment (FIG. 4A).
[00202] Further modifications to the modified endogenous λ light chain locus can be achieved with using similar techniques to insert more hV gene segments. For example, schematic illustrations of two additional targeting constructs (+16-λ and +12-λ Targeting Vectors) used for progressive insertion of addition human hV gene segments are provided in FIG. 5A. As illustrated, additional genomic fragments containing specific human hN/λ gene segments are inserted into the modified endogenous λ light chain locus in successive steps using homology provided by the previous insertion of human λ light chain sequences. Upon recombination with each targeting construct illustrated, in sequential fashion, 28 additional hX λ gene segments are inserted into the modified endogenous λ light chain locus. This creates a chimeric locus that produces a λ light chain protein that comprises human Ν/λ-ϋλ gene segments linked to a mouse Ολ gene.
[00203] The above approaches to insert human λ light chain gene segments at the mouse λ locus, maintains the enhancers positioned downstream of the Ολ2-ϋλ4-Ολ4 gene segments (designated Enh 2.4, Enh and Enh 3.1 FIG. 4A and FIG. 5A). This approach results in a single modified allele at the endogenous mouse λ light chain locus (FIG. 7A).
[00204] Compositions and methods for making a mouse that expresses a light chain comprising hN/λ and ϋλ gene segments operably linked to a mouse CX gene segment, are provided, including compositions and method for making a mouse that expresses such genes from an endogenous mouse λ light chain locus. The methods include selectively rendering one endogenous mouse Ν/λ-ϋλ-Ολ gene cluster nonfunctional (e.g., by a targeted deletion), and employing a hX λ and ϋλ gene segments at the endogenous mouse λ light chain locus to express a hX λ domain in a mouse.
[00205] Alternatively, in a second approach, human λ light chain gene segments may be positioned at the endogenous κ light chain locus. The genetic modification, in various embodiments, comprises a deletion of the endogenous κ light chain locus. For example, to eliminate mouse κ light chains from the endogenous antibody repertoire a deletion of the mouse VK and JK gene segments can be made. Genetically modified mouse embryos, cells, and targeting constructs for making the mice, mouse embryos, and cells are also provided.
[00206] For the reasons stated above, the deletion of the mouse VK and JK gene segments employs a relatively minimal disruption. A schematic illustration (not to scale) of deleted mouse VK and JK gene segments is provided in FIG. 3. The endogenous mouse VK and JK gene segments are deleted via recombinase-mediated deletion of mouse sequences position between two precisely positioned targeting vectors each employing site-specific recombination sites. A first targeting vector (JK Targeting Vector) is employed in a first targeting event to delete the mouse JK gene segments. A second targeting vector (VK Targeting Vector) is employed in a second, sequential targeting event to delete a sequence located 5' of the most distal mouse VK gene segment. Both targeting vectors contain site-specific recombination sites thereby allowing for the selective deletion of both selection cassettes and all intervening mouse κ light chain sequences after a successful targeting has been achieved. The resulting deleted locus is functionally silenced in that no endogenous κ light chain can be produced. This modified locus can be used for the insertion of Ιινλ and J gene segments to create an endogenous mouse κ locus comprising hV and J gene segments, whereby, upon recombination at the modified locus, the animal produces λ light chains comprising rearranged hV and J gene segments operably linked to an endogenous mouse CK gene segment. Various targeting vectors comprising human λ light chain sequences can be used in conjunction with this deleted mouse κ locus to create a hybrid light chain locus containing human λ gene segments operably linked with a mouse CK region.
[00207] Thus, a second approach positions one or more human νλ gene segments are positioned at the mouse κ light chain locus contiguous with a single human J gene segment (12/1 -κ Targeting Vector, FIG. 4B).
[00208] In various embodiments, modifications to this approach can be made to add gene segments and/or regulatory sequences to optimize the usage of the human λ light chain sequences from the mouse κ locus within the mouse antibody repertoire.
[00209] In a third approach, one or more hV gene segments are positioned at the mouse K light chain locus contiguous with four hJ gene sequences (12/4-κ Targeting Vector FIG. 4B).
[00210] In a third approach, one or more ΙΆ/λ gene segments are positioned at the mouse K light chain locus contiguous with a human κ intergenic sequence and a single hJ gene sequence (12(κ)1 -κ Targeting Vector, FIG. 4B).
[0021 1] In a fourth approach, one or more hV gene segments are positioned at the mouse K light chain locus contiguous with a human κ intergenic sequence four Ι^λ gene sequences (12(κ)4-κ Targeting Vector FIG. 4B).
[0021 2] All of the above approaches to insert human λ light chain gene segments at the mouse K locus, maintain the κ intronic enhancer element upstream of the CK gene (designated Εκϊ, FIG. 4B and FIG. 5B) and the 3' κ enhancer downstream of the CK gene (designated Εκ3', FIG. 4B and FIG. 5B). The approaches result in four separate modified alleles at the endogenous mouse κ light chain locus (FIG. 7B).
[00213] In various embodiments, genetically modified mouse comprise a knockout of the endogenous mouse λ light chain locus. In one embodiment, the λ light chain locus is knocked out by a strategy that deletes the region spanning \/λ2 to ϋλ2, and the region spanning νλ1 to Cλ^ (FIG. 2). Any strategy that reduces or eliminates the ability of the endogenous λ light chain locus to express endogenous λ domains is suitable for use with embodiments in this disclosure.
Lambda Domain Antibodies from Genetically Modified Mice
[00214] Mice comprising human λ sequences at either the mouse κ or λ light chain locus will express a light chain that comprises a V region fused to a mouse CL (CK or CX) region. These are advantageously bred to mice that (a) comprise a functionally silenced light chain locus (e.g., a knockout of the endogenous mouse κ or λ light chain locus); (b) comprise an endogenous mouse λ light chain locus that comprises hV and hJ gene segments operably linked to an endogenous mouse C gene; (c) comprise an endogenous mouse κ light chain locus that comprises h and hJK gene segments operably linked to an endogenous mouse CK gene; and, (d) a mouse in which one κ allele comprises h s and hJ s; the other κ allele comprising hV s and hJ s; one λ allele comprising hV s and hJ s and one λ allele silenced or knocked out, or both λ alleles comprising hV s and hJ s; and, two heavy chain alleles that each comprise hVHs, hDHs, and hJHs.
[00215] The antibodies that comprise the hV domains expressed in the context of either CK or Ο are used to make fully human antibodies by cloning the nucleic acids encoding the hX λ domains into expression constructs that bear genes encoding human C . Resulting expression constructs are transfected into suitable host cells for expressing antibodies that display a fully hVX domain fused to hC .
EXAMPLES
[00216] The following examples are provided so as to describe how to make and use methods and compositions of the invention, and are not intended to limit the scope of what the inventors regard as their invention. Unless indicated otherwise, temperature is indicated in Celsius, and pressure is at or near atmospheric. Example I
Deletion of the Mouse Immunoglobulin Light Chain Loci
[00217] Various targeting constructs were made using VELOCIGENE® technology (see, e.g., US Pat. No. 6,586,251 and Valenzuela et al. (2003) High-throughput engineering of the mouse genome coupled with high-resolution expression analysis, Nature Biotech. 21 (6):652-659) to modify mouse genomic Bacterial Artificial Chromosome (BAC) libraries to inactivate the mouse κ and λ light chain loci.
[00218] Deletion of the mouse λ light chain locus. DNA from mouse BAC clone RP23-135k15 (Invitrogen) was modified by homologous recombination to inactivate the endogenous mouse λ light chain locus through targeted deletion of the νλ-ϋλ-ΰλ gene clusters (FIG. 2).
[00219] Briefly, the entire proximal cluster comprising VX1-J 3-C 3-J 1-C 1 gene segments was deleted in a single targeting event using a targeting vector comprising a neomycin cassette flanked by loxP sites with a 5' mouse homology arm containing sequence 5' of the νλ1 gene segment and a 3' mouse homology arm containing sequence 3' of the C 1 gene segment (FIG. 2, Targeting Vector 1).
[00220] A second targeting construct was prepared to precisely delete the distal endogenous mouse λ gene cluster containing νλ2-ϋλ2-ΰλ2-ϋλ4-ΰλ4 except that the targeting construct contained a 5' mouse homology arm that contained sequence 5' of the νλ2 gene segment and a 3' mouse homology arm that contained sequence 5' to the endogenous C 2 gene segment (FIG. 2, Targeting Vector 2). Thus, the second targeting construct precisely deleted V 2-JX2, while leaving C 2-JX4-C 4 intact at the endogenous mouse λ locus. ES cells containing an inactivated endogenous λ locus (as described above) were confirmed by karyotyping and screening methods (e.g., TAQMAN®) known in the art. DNA was then isolated from the modified ES cells and subjected to treatment with CRE recombinase thereby mediating the deletion of the proximal targeting cassette containing the neomycin marker gene, leaving only a single loxP site at the deletion point (FIG. 2, bottom).
[00221] Deletion of the mouse κ light chain locus. Several targeting constructs were made using similar methods described above to modify DNA from mouse BAC clones RP23-302g12 and RP23-254m04 (Invitrogen) by homologous recombination to inactivate the mouse κ light chain locus in a two-step process (FIG. 3).
[00222] Briefly, the JK gene segments (1-5) of the endogenous mouse κ light chain locus were deleted in a single targeting event using a targeting vector comprising a hygromycin-thymidine kinase (hyg-TK) cassette containing a single loxP site 3' to the hyg- T cassette (FIG. 3, JK Targeting Vector). The homology arms used to make this targeting vector contained mouse genomic sequence 5' and 3' of the endogenous mouse JK gene segments. In a second targeting event, a second targeting vector was prepared to delete a portion of mouse genomic sequence upstream (5') to the most distal endogenous mouse VK gene segment (FIG. 3, VK Targeting Vector). This targeting vector contained an inverted /ox51 1 site, a loxP site and a neomycin cassette. The homology arms used to make this targeting vector contained mouse genomic sequence upstream of the most distal mouse VK gene segment. The targeting vectors were used in a sequential fashion (i.e., JK then VK) to target DNA in ES cells. ES bearing a double-targeted chromosome (i.e., a single endogenous mouse κ locus targeted with both targeting vectors) were confirmed by karyotyping and screening methods (e.g., Taqman™) known in the art. DNA was then isolated from the modified ES cells and subjected to treatment with Cre recombinase thereby mediating the deletion of endogenous mouse VK gene segments and both selection cassettes, while leaving two juxtaposed lox sites in opposite orientation relative to one another (FIG. 3, bottom; SEQ ID NO:1 ).
[00223] Thus, two modified endogenous light chain loci (κ and λ) containing intact enhancer and constant regions were created for progressively inserting unrearranged human λ germline gene segments in a precise manner using targeting vectors described below.
Example II
Replacement of Mouse Light Chain Loci
with a Human λ Light Chain Mini-Locus
[00224] Multiple targeting vectors were engineered for progressive insertion of human λ gene segments into the endogenous mouse κ and λ light chain loci using similar methods as described above. Multiple independent initial modifications were made to the endogenous light chain loci each producing a chimeric light chain locus containing hV and ϋλ gene segments operably linked to mouse light chain constant genes and enhancers.
[00225] A human λ mini-locus containing 12 human V and one human JX gene segment. A series of initial targeting vectors were engineered to contain the first 12 consecutive human V gene segments from cluster A and a hJ 1 gene segment or four hJ gene segments using a human BAC clone named RP1 1 -729g4 (Invitrogen). FIGs. 4A and 4B show the targeting vectors that were constructed for making an initial insertion of human λ light chain gene segments at the mouse λ and κ light chain loci, respectively.
[00226] For a first set of initial targeting vectors, a 124,125 bp DNA fragment from the 729g4 BAC clone containing 12 hV gene segments and a hJ 1 gene segment was engineered to contain a Pl-Scel site 996 bp downstream (3') of the hJX1 gene segment for ligation of a 3' mouse homology arm. Two different sets of homology arms were used for ligation to this human fragment; one set of homology arms contained endogenous mouse λ sequences from the 135k15 BAC clone (FIG.4A) and another set contained endogenous κ sequence 5' and 3' of the mouse VK and J gene segments from mouse BAC clones RP23-302g12 and RP23-254m04, respectively (FIG. 4B).
[00227] For the 12/1-λ Targeting Vector (FIG. 4A), a Pl-Scel site was engineered at the 5' end of a 27,847 bp DNA fragment containing the mouse Ολ2-ϋλ4-Ολ4 and enhancer 2.4 of the modified mouse λ locus described in Example 1. The ~28 kb mouse fragment was used as a 3' homology arm by ligation to the ~124 kb human λ fragment, which created a 3' junction containing, from 5' to 3', a Ιιϋλΐ gene segment, 996 bp of human λ sequence 3' of the hJ 1 gene segment, 1229 bp of mouse λ sequence 5' to the mouse 0X2 gene, the mouse C 2 gene and the remaining portion of the ~28 kb mouse fragment. Upstream (5') from the human V 3-12 gene segment was an additional 1456 bp of human λ sequence before the start of the 5' mouse homology arm, which contained 23,792 bp of mouse genomic DNA corresponding to sequence 5' of the endogenous mouse λ locus. Between the 5' homology arm and the beginning of the human λ sequence was a neomycin cassette flanked by Frt sites.
[00228] Thus, the 12/1-λ Targeting Vector included, from 5' to 3', a 5' homology arm containing ~24 kb of mouse λ genomic sequence 5' of the endogenous λ locus, a 5' Frt site, a neomycin cassette, a 3' Frt site, ~123 kb of human genomic λ sequence containing the first 2 consecutive hV gene segments and a Ιηϋλΐ gene segment, a Pl-Scel site, and a 3' homology arm containing ~28 kb of mouse genomic sequence including the endogenous Ολ2-ϋλ4-Ολ4 gene segments, the mouse enhancer 2.4 sequence and additional mouse genomic sequence downstream (3') of the enhancer 2.4 (FIG. 4A).
[00229] In a similar fashion, the 12/1-κ Targeting Vector (FIG. 4B) employed the same ~124 human λ fragment with the exception that mouse homology arms containing mouse κ sequence were used such that targeting to the endogenous κ locus could be achieved by homologous recombination. Thus, the 12/1 -κ Targeting Vector included, from 5' to 3', a 5' homology arm containing ~23 kb of mouse genomic sequence 5' of the endogenous κ locus, an l-Ceul site, a 5' Frt site, a neomycin cassette, a 3' Frt site, ~124 kb of human genomic λ sequence containing the first 12 consecutive Ιινλ gene segments and a hJ 1 gene segment, a Pl-Scel site, and a 3' homology arm containing ~28 kb of mouse genomic sequence including the endogenous the mouse CK gene, Εκϊ and Εκ3' and additional mouse genomic sequence downstream (3') of Εκ3' (FIG. 4B, 12/1-κ Targeting Vector). [00230] Homologous recombination with either of these two initial targeting vectors created a modified mouse light chain locus (κ or λ) containing 12 hN λ gene segments and a Ριϋλΐ gene segment operably linked to the endogenous mouse light chain constant gene and enhancers (CK or C 2 and Εκί/Εκ3' or Enh 2.4/Enh 3.1 ) gene which, upon
recombination, leads to the formation of a chimeric λ light chain.
[00231] A human λ mini-locus with 12 human V and four human ϋλ gene segments. In another approach to add diversity to a chimeric λ light chain locus, a third initial targeting vector was engineered to insert the first 12 consecutive human V gene segments from cluster A and hJ 1 , 2, 3 and 7 gene segments into the mouse κ light chain locus (FIG. 4B, 12/4-κ Targeting Vector). A DNA segment containing hJ 1 , JX2, ϋλ3 and ϋλ7 gene segments was made by de novo DNA synthesis (Integrated DNA Technologies) including each ϋλ gene segment and human genomic sequence of ~100 bp from both the immediate 5' and 3' regions of each ϋλ gene segment. A Pl-Scel site was engineered into the 3' end of this ~1 kb DNA fragment and ligated to a chloroamphenicol cassette.
Homology arms were PCR amplified from human λ sequence at 5' and 3' positions relative to the bJX1 gene segment of the human BAC clone 729g4. Homologous recombination with this intermediate targeting vector was performed on a modified 729g4 BAC clone that had been previously targeted upstream (5') of the human νλ3-12 gene segment with a neomycin cassette flanked by Frt sites, which also contained an l-Ceul site 5' to the 5' Frt site. The double-targeted 729g4 BAC clone included from 5' to 3' an l-Ceul site, a 5' Frt site, a neomycin cassette, a 3' Frt site, a ~123 kb fragment containing the first 12 hV gene segments, a ~1 kb fragment containing human ϋλ1 , 2, 3 and 7 gene segments, a Pl-Scel site, and a chloroamphenicol cassette. This intermediate targeting vector was digested together with l-Ceul and Pl-Scel and subsequently ligated into the modified mouse BAC clone (described above) to create the third targeting vector.
[00232] This ligation resulted in a third targeting vector for insertion of human λ sequences into the endogenous κ light chain locus, which included, from 5' to 3', a 5' mouse homology arm containing ~23 kb of genomic sequence 5' of the endogenous mouse K locus, an l-Ceul site, a 5' Frt site, a neomycin cassette, a 3' Frt site, a -123 kb fragment containing the first 12 hV gene segments, a ~1 kb fragment containing Ιιϋλ1 , 2, 3 and 7 gene segments, a Pl-Scel site and a 3' homology arm containing -28 kb of mouse genomic sequence including the endogenous the mouse CK gene, Εκϊ and Εκ3' and additional mouse genomic sequence downstream (3') of Ε 3' (FIG. 4B, 12/4-κ Targeting Vector). Homologous recombination with this third targeting vector created a modified mouse K light chain locus containing 12 V gene segments and four J gene segments operably linked to the endogenous mouse CK gene which, upon recombination, leads to the formation of a chimeric human λ/mouse κ light chain.
[00233] A human λ mini-locus with an integrated human κ light chain sequence.
In a similar fashion, two additional targeting vectors similar to those engineered to make an initial insertion of human λ gene segments into the endogenous κ light chain locus (FIG. 4B, 12/1 -K and 12/4-κ Targeting Vectors) were engineered to progressively insert human λ light chain gene segments using uniquely constructed targeting vectors containing contiguous human λ and κ genomic sequences. These targeting vectors were constructed to include a ~ 23 kb human κ genomic sequence naturally located between human V 4-1 and JK1 gene segments. This human κ genomic sequence was specifically positioned in these two additional targeting vectors between human V and human ϋλ gene segments (FIG. 4B, 12(K)1 -K and 12(κ)4-κ Targeting Vectors).
[00234] Both targeting vectors containing the human κ genomic sequence were made using the modified RP1 1 -729g4 BAC clone described above (FIG. 6). This modified BAC clone was targeted with a spectinomycin selection cassette flanked by Notl and AsiSI restriction sites (FIG.6, top left). Homologous recombination with the spectinomycin cassette resulted in a double-targeted 729g4 BAC clone which included, from 5' to 3', an I- Ceul site, a 5' Frt site, a neomycin cassette, a 3' Frt site, a ~123 kb fragment containing the first 12 hV gene segments, a Notl site about 200 bp downstream (3') to the nonamer sequence of the hV 3-1 gene segment, a spectinomycin cassette and an AsiSI site. A separate human BAC clone containing human κ sequence (CTD-2366j12) was targeted two independent times to engineer restriction sites at locations between h 4-1 and hJKl gene segments to allow for subsequent cloning of a -23 kb fragment for ligation with the hV gene segments contained in the double targeted modified 729g4 BAC clone (FIG. 6, top right).
[00235] Briefly, the 2366j12 BAC clone is about 132 kb in size and contains hVx gene segments 1 -6, 1 -5, 2-4, 7-3, 5-2, 4-1 , human κ genomic sequence down stream of the VK gene segments, hJK gene segments 1 -5, the hCic and about 20 kb of additional genomic sequence of the human κ locus. This clone was first targeted with a targeting vector containing a hygromycin cassette flanked by Frt sites and a Notl site downstream (3') of the 3' Frt site. The homology arms for this targeting vector contained human genomic sequence 5' and 3' of the VK gene segments within the BAC clone such that upon homologous recombination with this targeting vector, the VK gene segments were deleted and a Notl site was engineered -133 bp downstream of the h 4-1 gene segment (FIG. 6, top right). This modified 2366j12 BAC clone was targeted independently with two targeting vectors at the 3' end to delete the IIJK gene segments with a chloroamphenicol cassette that also contained either a Ιιϋλΐ gene segment, a Pl-Scel site and an AsiSI site or a human λ genomic fragment containing four MX gene segments (supra), a Pl-Scel site and an AsiSI site (FIG. 6, top right). The homology arms for these two similar targeting vectors contained sequence 5' and 3' of the hJK gene segments. Homologous recombination with these second targeting vectors and the modified 2366J12 BAC clone yielded a double- targeted 2366j12 clone which included, from 5' to 3', a 5' Frt site, a hygromycin cassette, a 3' Frt site, a Notl site, a 22,800 bp genomic fragment of the human κ locus containing the intergenic region between the 4-1 and JK1 gene segments, either a Κιϋλΐ gene segment or a human λ genomic fragment containing ηϋλ1 , ϋλ2, JX3 and ϋλ7, a Pl-Scel site and a chloroamphenicol cassette (FIG. 6, top right). Two final targeting vectors to make the two additional modifications were achieved by two ligation steps using the double-targeted 729g4 and 2366j12 clones.
[00236] Double targeted 729g4 and 2366j12 clones were digested with Notl and AsiSI yielding one fragment containing the neomycin cassette and hX λ gene segments and another fragment containing the ~23 kb genomic fragment of the human κ locus containing the intergenic region between the VK4-1 and JK1 gene segments, either a hJ 1 gene segment or a genomic fragment containing hJ 1 , J 2, ϋλ3 and ϋλ7 gene segments, the Pl- Scel site and the chloroamphenicol cassette, respectively. Ligation of these fragments generated two unique BAC clones containing from 5' to 3' the hV gene segments, the human κ genomic sequence between the VK4-1 and JK1 gene segments, either a hJ 1 gene segment or a genomic fragment containing hJ 1 , J 2, ϋλ3 and JX7 gene segments, a Pl-Scel site and a chloroamphenicol cassette (FIG. 6, bottom). These new BAC clones were then digested with l-Ceul and Pl-Scel to release the unique fragments containing the upstream neomycin cassette and the contiguous human λ and κ sequences and ligated into a modified mouse BAC clone 302g12 which contained from 5' to 3' mouse genomic sequence 5' of the endogenous κ locus, an l-Ceul site, a 5' Frt site, a neomycin cassette, a 3' Frt site, hN λ gene segments (3-12 to 3-1 ), a Notl site -200 bp downstream of \A3-1 , ~23 kb of human κ sequence naturally found between the human VK4-1 and JK1 gene segments, either a Ιιϋλΐ gene segment or a genomic fragment containing Ιιϋλΐ , ϋλ2, ϋλ3 and JX7 gene segments, the mouse Εκί, the mouse CK gene and Εκ3' (FIG. 4, 12η\/λ- Χ/κϋ -ΙιϋλΙ and 12hV -ViiJK-4hJ Targeting Vectors). Homologous recombination with both of these targeting vectors created two separate modified mouse κ light chain loci containing 12 hX/λ gene segments, human κ genomic sequence, and either one or four Ιιϋλ gene segments operably linked to the endogenous mouse CK gene which, upon
recombination, leads to the formation of a chimeric human λ/mouse κ light chain.
Example III
Engineering Additional Human νλ Genes Segments
Into a Human λ Light Chain Mini-Locus
[00237] Additional hX λ gene segments were added independently to each of the initial modifications described in Example 2 using similar targeting vectors and methods (FIG. 5A, +16-λ Targeting Vector and FIG. 5B, +16-κ Targeting Vector).
[00238] Introduction of 16 additional human VX gene segments. Upstream (5 ) homology arms used in constructing targeting vectors for adding 16 additional hVX gene segments to the modified light chain loci described in Example 2 contained mouse genomic sequence 5' of either the endogenous κ or λ light chain loci. The 3' homology arms were the same for all targeting vectors and contained human genomic sequence overlapping with the 5' end of the human λ sequence of the modifications as described in Example 2.
[00239] Briefly, two targeting vectors were engineered for introduction of 16 additional hV gene segments to the modified mouse light chain loci described in Example 2 (FIG. 5A and 5B, +16-λ or +16-κ Targeting Vector). A ~172 kb DNA fragment from human BAC clone RP1 1-761113 (Invitrogen) containing 21 consecutive hVX gene segments from cluster A was engineered with a 5' homology arm containing mouse genomic sequence 5' to either the endogenous κ or λ light chain loci and a 3' homology arm containing human genomic λ sequence. The 5' mouse κ or λ homology arms used in these targeting constructs were the same 5' homology arms described in Example 2 (FIG. 5A and 5B). The 3' homology arm included a 53,057 bp overlap of human genomic λ sequence corresponding to the equivalent 5' end of the ~123 kb fragment of human genomic λ sequence described in Example 2. These two targeting vectors included, from 5' to 3', a 5' mouse homology arm containing either ~23 kb of genomic sequence 5' of the endogenous mouse κ light chain locus or ~24 kb of mouse genomic sequence 5' of the endogenous λ light chain locus, a 5' Frt site, a hygromycin cassette, a 3' Fit site and 171 ,457 bp of human genomic λ sequence containing 21 consecutive ηνλ gene segments, ~53 kb of which overlaps with the 5' end of the human λ sequence described in Example 3 and serves as the 3' homology arm for this targeting construct (FIG. 5A and 5B, +16-λ or +16-κ Targeting Vectors). Homologous recombination with these targeting vectors created independently modified mouse κ and λ light chain loci each containing 28 hV gene segments and a hJ 1 gene segment operably linked to endogenous mouse constant genes (CK or CX2) which, upon recombination, leads to the formation of a chimeric light chain.
[00240] In a similar fashion, the +16-κ Targeting Vector was also used to introduce the 16 additional hX λ gene segments to the other initial modifications described in Example 2 that incorporated multiple Ιιϋλ gene segments with and without an integrated human κ sequence (FIG. 4B). Homologous recombination with this targeting vector at the endogenous mouse κ locus containing the other initial modifications created mouse κ light chain loci containing 28 hN λ gene segments and hJ 1 , 2, 3 and 7 gene segments with and without a human VK-JK genomic sequence operably linked to the endogenous mouse CK gene which, upon recombination, leads to the formation of a chimeric λ-κ light chain.
[00241] Introduction of 12 additional human VX gene segments. Additional hN/λ gene segments were added independently to each of the modifications described above using similar targeting vectors and methods. The final locus structure resulting from homologous recombination with targeting vectors containing additional hVX gene segments are shown in FIG. 7A and 7B.
[00242] Briefly, a targeting vector was engineered for introduction of 12 additional hX λ gene segments to the modified mouse κ and λ light chain loci described above (FIG. 5A and 5B, +12-λ or 2-κ Targeting Vectors). A 93,674 bp DNA fragment from human BAC clone RP1 1-22118 (Invitrogen) containing 12 consecutive hV gene segments from cluster B was engineered with a 5' homology arm containing mouse genomic sequence 5' to either the endogenous mouse κ or λ light chain loci and a 3' homology arm containing human genomic λ sequence. The 5' homology arms used in this targeting construct were the same 5' homology arms used for the addition of 16 hVX gene segments described above (FIG. 5A and 5B). The 3' homology arm was made by engineering a Pl-Scel site ~3431 bp 5' to the human VX3-29P gene segment contained in a 27,468 bp genomic fragment of human λ sequence from BAC clone RP1 1-761113. This Pl-Scel site served as a ligation point to join the ~94 kb fragment of additional human λ sequence to the ~27 kb fragment of human λ sequence that overlaps with the 5' end of the human λ sequence in the previous modification using the +16-λ or +16-κ Targeting Vectors (FIG. 5A and 5B). These two targeting vectors included, from 5' to 3', a 5' homology arm containing either ~23 kb of mouse genomic sequence 5' of the endogenous κ light chain locus or ~24 kb of mouse genomic sequence 5' of the endogenous λ light chain locus, a 5' Frt site, a neomycin cassette, a 3' Frt site and 121 ,188 bp of human genomic λ sequence containing 16 hVX gene segments and a Pl-Scel site, ~27 kb of which overlaps with the 5' end of the human λ sequence from the insertion of 16 addition hV gene segments and serves as the 3' homology arm for this targeting construct (FIG. 5A and 5B, +12-λ or 12-κ Targeting Vectors). Homologous recombination with these targeting vectors independently created modified mouse κ and λ light chain loci containing 40 hV gene segments and human ϋλ1 operably linked to the endogenous mouse constant genes (CK or C 2) which, upon recombination, leads to the formation of a chimeric light chain (bottom of FIG.5A and 5B).
[00243] In a similar fashion, the +12-κ Targeting Vector was also used to introduce the 12 additional hV gene segments to the other initial modifications that incorporated multiple hJ gene segments with and without an integrated human κ sequence (FIG. 4B). Homologous recombination with this targeting vector at the endogenous mouse κ locus containing the other modifications created a mouse κ light chain locus containing 40 hV gene segments and ηϋλ1 , 2, 3 and 7 gene segments with and without a human VK-JK genomic sequence operably linked to the endogenous mouse CK gene which, upon recombination, leads to the formation of a chimeric λ-κ light chain.
Example IV
Identification of targeted ES cells Bearing
Human λ Light Chain Gene Segments
[00244] Targeted BAC DNA made according to the foregoing Examples was used to electroporate mouse ES cells to create modified ES cells for generating chimeric mice that express human λ light chain gene segments. ES cells containing an insertion of unrearranged human λ light chain gene segments were identified by a quantitative TAQMAN® assay. Specific primers sets and probes were design for insertion of human λ sequences and associated selection cassettes (gain of allele, GOA), loss of endogenous mouse sequences and any selection cassettes (loss of allele, LOA) and retention of flanking mouse sequences (allele retention, AR). For each additional insertion of human λ sequences, additional primer sets and probes were used to confirm the presence of the additional human λ sequences as well as the previous primer sets and probes used to confirm retention of the previously targeted human sequences. Table 1 sets forth the primers and associated probes used in the quantitative PCR assays. Table 2 sets forth the combinations used for confirming the insertion of each section of human λ light chain gene segments in ES cell clones.
[00245] ES cells bearing the human λ light chain gene segments are optionally transfected with a construct that expresses FLP in order to remove the Fifed neomycin cassette introduced by the insertion of the targeting construct containing human νλ5-52 - V 1 -40 gene segments (FIG. 5A and 5B). The neomycin cassette may optionally be removed by breeding to mice that express FLP recombinase (e.g., US 6,774,279). Optionally, the neomycin cassette is retained in the mice.
Table 1
Primer SEQ ID NO: Probe SEQ ID NO:
Figure imgf000049_0001
Figure imgf000050_0001
Table 2
Figure imgf000050_0002
68h2F/68h2R 68h2P
hV 5-52 - hV 1 -40
GOA 68h5F/68h5R 68h5P
NeoF/NeoR NeoP Neomycin cassette
HygF/HygR HygP Hygromycin cassette mI_1 F/mi_1 R mL1 P Mouse νλ1 -Ολ1
LOA mL2F/mL2R mL2P Cluster
mL11 F/mL1 1 R mL1 1 P Mouse V 2-C 2
Insertion of mL12F/mL12R mL12P Cluster
12 ηΥλ
hL2F/hL2R hL2P
hV 3-12 - hV 3-1 hl_3F/hl_3R hL3P
AR
67hT1 F/67hT1 R 67hT1 P
hV 3-27 hV 3-12
67hT3F/67hT3R 67hT3P
Mouse sequence in 5'
MKD2F/MKD2R MKD2P
VK locus
AR/LOA
Mouse sequence in 3'
MKP15F/MKP15R MKP15P
VK locus
Example V
Generation of Mice Expressing Human λ Light Chains
From an Endogenous Light Chain Locus
[00246] Targeted ES cells described above were used as donor ES cells and introduced into an 8-cell stage mouse embryo by the VELOCIMOUSE® method (see, e.g., US Pat. No. 7,294,754 and Poueymirou et al. (2007) F0 generation mice that are essentially fully derived from the donor gene-targeted ES cells allowing immediate phenotypic analyses Nature Biotech. 25(1 ):91-99. VELOCIMICE® (F0 mice fully derived from the donor ES cell) independently bearing human λ gene segments were identified by genotyping using a modification of allele assay (Valenzuela et al., supra) that detected the presence of the unique human λ gene segments (supra).
[00247] κ:λ light chain usage of mice bearing human λ light chain gene segments.
Mice homozygous for each of three successive insertions of h\A, gene segments with a single hJ gene segment (FIG. 5B) and mice homozygous for a first insertion of hVX gene segments with either a single hJ gene segment or four human JX gene segments including a human VK-JK genomic sequence (FIG. 4B) were analyzed for κ and λ light chain expression in splenocytes using flow cytometry.
[00248] Briefly, spleens were harvested from groups of mice (ranging from three to seven animals per group) and grinded using glass slides. Following lysis of red blood cells (RBCs) with ACK lysis buffer (Lonza Walkersville), splenocytes were stained with fluorescent dye conjugated antibodies specific for mouse CD19 (Clone 1 D3; BD Biosciences), mouse CD3 (17A2; Biolegend), mouse IgK (187.1 ; BD Biosciences) and mouse Ig (RML-42; Biolegend). Data was acquired using a BD™ LSR II flow cytometer (BD Biosciences) and analyzed using FLOWJO™ software (Tree Star, Inc.). Table 3 sets forth the average percent values for B cells (CD19+), κ light chain
Figure imgf000052_0001
and λ light chain (CD19+lg ~lg +) expression observed in splenocytes from groups of animals bearing each genetic modification.
[00249] In a similar experiment, B cell contents of the splenic compartment from mice homozygous for a first insertion of 12 hN/λ and four Ιιϋλ gene segments including a human VK-JK genomic sequence operably linked to the mouse CK gene (bottom of FIG. 4B) and mice homozygous for 40 hN λ and one ηϋλ gene segment (bottom of FIG. 5B or top of FIG. 7B) were analyzed for IgK and \gX expression using flow cytometry (as described above). FIG. 8A shows the \gX and Ig expression in CD19+ B cells for a representative mouse from each group. The number of CD19+ B cells per spleen was also recorded for each mouse (FIG. 8B).
[00250] In another experiment, B cell contents of the spleen and bone marrow compartments from mice homozygous for 40 hV and four hJ gene segments including a human VK-JK genomic sequence operably linked to the mouse CK gene (bottom of FIG. 7B) were analyzed for progression through B cell development using flow cytometry of various cell surface markers.
[00251] Briefly, two groups (N=3 each, 9-12 weeks old, male and female) of wild type and mice homozygous for 40 ΙιΝ/λ and four bJk gene segments including a human VK-JK genomic sequence operably linked to the mouse CK gene were sacrificed and spleens and bone marrow were harvested. Bone marrow was collected from femurs by flushing with complete RPMI medium (RP I medium supplemented with fetal calf serum, sodium pyruvate, Hepes, 2-mercaptoethanol, non-essential amino acids, and gentamycin). RBCs from spleen and bone marrow preparations were lysed with ACK lysis buffer (Lonza Walkersville), followed by washing with complete RPMI medium. 1 x106 cells were incubated with anti-mouse CD16/CD32 (2.4G2, BD Biosciences) on ice for 10 minutes, followed by labeling with a selected antibody panel for 30 min on ice.
[00252] Bone marrow panel: anti-mouse FITC-CD43 (1 B1 1 , BioLegend), PE-ckit (2B8, BioLegend), PeCy7-lgM (11/41 , eBioscience), PerCP-Cy5.5-lgD (1 1 -26c.2a, BioLegend), APC- B220 (RA3-6B2, eBioscience), APC-H7-CD19 (ID3, BD) and Pacific Blue-CD3 (17A2, BioLegend).
[00253] Bone marrow and spleen panel: anti-mouse FITC-lgK (187.1 , BD), PE-lgX (RML-42, BioLegend), PeCy7-lgM (11/41 , ebioscience), PerCP-Cy5.5-lgD (1 1 -26c.2a, BioLegend), Pacific Blue-CD3 (17A2, BioLegend), APC- B220 (RA3-6B2, eBioscience), APC-H7-CD19 (ID3, BD).
[00254] Following staining, cells were washed and fixed in 2% formaldehyde. Data acquisition was performed on a FACSCANTOII™ flow cytometer (BD Biosciences) and analyzed with FLOWJO™ software (Tree Star, Inc.). FIGs. 9A - 9D show the results for the splenic compartment of one representative mouse from each group. FIGs. 10A - 10E show the results for the bone marrow compartment of one representative mouse from each group. Table 4 sets forth the average percent values for B cells (CD19+), κ light chain (CD19+lgK+lg ~), and λ light chain (CD19+lgK~lg +) expression observed in splenocytes from groups of animals bearing various genetic modifications. Table 5 sets forth the average percent values for B cells (CD19+), mature B cells (B220hllgM+), immature B cells (B220intlgM+), immature B cells expressing κ light chain (B220intlgM+lgK+) and immature B cells expressing λ light chain (B220intlgM+^+) observed in bone marrow of wild type and mice homozygous for 40 hN λ and four hJX gene segments including a human V -JK genomic sequence operably linked to the mouse CK gene. This experiment was repeated with additional groups of the mice described above and demonstrated similar results (data not shown).
Figure imgf000053_0001
Table 5
% % % % %
Genotype B Mature Immature Immature Immature
cells B cells B cells lgi + B cells lgX+ B cells
Wild Type 62.2 9.2 12.0 79.0 8.84
40hVX-
60.43 2.59 7.69 38.29 43.29
[00255] Human V gene usage in mice bearing human λ light chain gene segments. Mice heterozygous for a first insertion of human λ sequences (η\/λ3-12 - h\A.3-1 and hJ 1 , FIG. 5B) and homozygous for a third insertion of human λ sequences (hV 5-52 - hV 3-1 and hJ 1 , FIG. 5B) were analyzed for human λ light chain gene usage by reverse-transcriptase polymerase chain reaction (RT-PCR) using RNA isolated from splenocytes.
[00256] Briefly, spleens were harvested and perfused with 10 ml. RPMI-1640 (Sigma) with 5% HI-FBS in sterile disposable bags. Each bag containing a single spleen was then placed into a STOMACHER™ (Seward) and homogenized at a medium setting for 30 seconds. Homogenized spleens were filtered using a 0.7pm cell strainer and then pelleted with a centrifuge (1000 rpm for 10 minutes) and RBCs were iysed in BD PHARM LYSE™ (BD Biosciences) for three minutes. Splenocytes were diluted with RPMI-1640 and centrifuged again, followed by resuspension in 1 mL of PBS (Irvine Scientific). RNA was isolated from pelleted splenocytes using standard techniques known in the art.
[00257] RT-PCR was performed on splenocyte RNA using primers specific for human hN/λ gene segments and the mouse CK gene (Table 6). PCR products were gel-purified and cloned into pCR2.1 -TOPO TA vector (Invitrogen) and sequenced with primers M13 Forward (GTAAAACGAC GGCCAG; SEQ ID NO:55) and M13 Reverse (CAGGAAACAG CTATGAC; SEQ ID NO:56) located within the vector at locations flanking the cloning site. Eighty-four total clones derived from the first and third insertions of human λ sequences were sequenced to determine hX λ gene usage (Table 7). The nucleotide sequence of the hV -hJ 1-mCK junction for selected RT-PCR clones is shown in FIG. 1 1.
[00258] In a similar fashion, mice homozygous for a third insertion of human λ light chain gene sequences (i.e. 40 hN λ gene segments and four hJX gene segments including a human VK-JK genomic sequence, bottom of FIG. 7B) operably linked to the endogenous mouse CK gene were analyzed for human λ light chain gene usage by RT-PCR using RNA isolated from splenocytes (as described above). The human λ light chain gene segment usage for 26 selected RT-PCR clones are shown in Table 8. The nucleotide sequence of the hV -hJ -mCK junction for selected RT-PCR clones is shown in FIG. 12.
[00259] In a similar fashion, mice homozygous for a first insertion of human λ light chain gene segments (12 hVX gene segments and hJ 1 , FIG. 4A & FIG. 5A) operably linked to the endogenous mouse Ολ2 gene were analyzed for human λ light chain gene usage by RT-PCR using RNA isolated from splenocytes (as described above). The primers specific for hVX gene segments (Table 6) were paired with one of two primers specific for the mouse CX2 gene; CX2-1 (SEQ ID NO:104) or C 2-2 (SEQ ID NO: 105).
[00260] Multiple hN λ gene segments rearranged to h 1 were observed from the RT- PCR clones from mice bearing human λ light chain gene segments at the endogenous mouse λ light chain locus. The nucleotide sequence of the hVX-hJX-m^2 junction for selected RT-PCR clones is shown in FIG. 13.
Table 6
Figure imgf000055_0001
Table 7 Table 8
Observed No.
ηΥλ
of Clones
Figure imgf000056_0001
Figure imgf000056_0002
[00261] FIG. 1 1 shows the sequence of the η\/λ-ηϋλ1-η"ΐΟκ junction for RT-PCR clones from mice bearing a first and third insertion of hX λ gene segments with a single hJ gene segment. The sequences shown in FIG. 1 1 illustrate unique rearrangements involving different hN λ gene segments with hJX1 recombined to the mouse CK gene. Heterozygous mice bearing a single modified endogenous κ locus containing 12 hN/λ gene segments and hJ 1 and homozygous mice bearing two modified endogenous κ loci containing 40 hN λ gene segments and Ιιϋλ1 were both able to produce human λ gene segments operably linked to the mouse CK gene and produce B cells that expressed human λ light chains. These rearrangements demonstrate that the chimeric loci were able to independently rearrange human λ gene segments in multiple, independent B cells in these mice. Further, these modifications to the endogenous κ light chain locus did not render any of the h\A, gene segments inoperable or prevent the chimeric locus from recombining multiple hV and a Ιιϋλ (ϋλ1 ) gene segment during B cell development as evidenced by 16 different hVX gene segments that were observed to rearrange with Ιιϋλΐ (Table 7). Further, these mice made functional antibodies containing rearranged human \/λ-ϋλ gene segments operably linked to mouse CK genes as part of the endogenous immunoglobulin light chain repertoire.
[00262] FIG. 12 shows the sequence of the
Figure imgf000057_0001
junction for selected RT-PCR clones from mice homozygous for 40 hX λ and four Ιιϋλ gene segments including a human VK-JK genomic sequence. The sequences shown in FIG. 12 illustrate additional unique rearrangements involving multiple different hX λ gene segments, spanning the entire chimeric locus, with multiple different ηϋλ gene segments rearranged and operably linked to the mouse CK gene. Homozygous mice bearing modified endogenous κ loci containing 40 hVX and four J gene segments were also able to produce human λ gene segments operably linked to the mouse CK gene and produce B cells that expressed human λ light chains. These rearrangements further demonstrate that the all stages of chimeric loci were able to independently rearrange human λ gene segments in multiple, independent B cells in these mice. Further, these additional modifications to the endogenous κ light chain locus demonstrates that each insertion of human λ gene segments did not render any of the hVX and/or ϋλ gene segments inoperable or prevent the chimeric locus from
recombining the hX λ and ϋλ gene segments during B cell development as evidenced by 12 different hN λ gene segments that were observed to rearrange with all four Jk gene segments (Table 8) from the 26 selected RT-PCR clone. Further, these mice as well made functional antibodies containing human Ν/λ-ϋλ gene segments operably linked to mouse CK regions as part of the endogenous immunoglobulin light chain repertoire.
[00263] FIG. 13 shows the sequence of the hV -hJ -mC 2 junction for three individual RT-PCR clones from mice homozygous for 12 hN λ gene segments and hJ 1 . The sequences shown in FIG. 13 illustrate additional unique rearrangements involving different hV gene segments, spanning the length of the first insertion, with hJ 1 rearranged and operably linked to the mouse C 2 gene (2D1 = VX2-8JX1 ; 2D9 = V 3-10ϋλ1 ; 3E15 = V 3- 1 ϋλ1 ). One clone demonstrated a nonproductive rearrangement due to N additions at the hV -hJ junction (2D1 , FIG.13). This is not uncommon in V(D)J recombination, as the joining of gene segments during recombination has been shown to be imprecise. Although this clone represents an unproductive recombinant present in the light chain repertoire of these mice, this demonstrates that the genetic mechanism that contributes to junctional diversity among antibody genes is operating normally in these mice and leading to an antibody repertoire containing light chains with greater diversity.
[00264] Homozygous mice bearing modified endogenous λ loci containing 12 hX λ gene segments and hJX1 were also able to produce human λ gene segments operably linked to an endogenous mouse C gene and produce B cells that expressed reverse chimeric λ light chains containing hV regions linked to mouse C regions. These rearrangements further demonstrate that human λ light chain gene segments placed at the other light chain locus {i.e., the λ locus) were able to independently rearrange human λ gene segments in multiple, independent B cells in these mice. Further, the modifications to the endogenous λ light chain locus demonstrate that the insertion of human λ gene segments did not render any of the hX λ and/or hJX1 gene segments inoperable or prevent the chimeric locus from recombining the hVX and Ιιϋλΐ gene segments during B cell development. Further, these mice also made functional antibodies containing human νλ-ϋλ gene segments operably linked to a mouse Ολ region as part of the endogenous immunoglobulin light chain repertoire.
[00265] As shown in this Example, mice bearing human λ light chain gene segments at the endogenous κ and λ light chain loci are capable of rearranging human λ light chain gene segments and expressing them in the context of a mouse CK and/or C region as part of the normal antibody repertoire of the mouse because a functional light chain is required at various checkpoints in B cell development in both the spleen and bone marrow. Further, early subsets of B cells (e.g., pre-, pro- and transitional B cells) demonstrate a normal phenotype in these mice as compared to wild type littermates (FIGs. 9D, 10A and 10B). A small deficit in bone marrow and peripheral B cell populations was observed, which may be attributed to a deletion of a subset of auto-reactive immature B cells and/or a suboptimal association of human λ light chain with mouse heavy chain. However, the IgK/lg usage observed in these mice demonstrates a situation that is more like human light chain expression than that observed in mice.
Example VI
Breeding of Mice Expressing Human λ Light Chains
From an Endogenous Light Chain Locus
[00266] To optimize the usage of the human λ gene segments at an endogenous mouse light chain locus, mice bearing the unrearranged human λ gene segments are bred to another mouse containing a deletion in the opposing endogenous light chain locus (either κ or λ). For example, human λ gene segments positioned at the endogenous κ locus would be the only functional light chain gene segments present in a mouse that also carried a deletion in the endogenous λ light chain locus. In this manner, the progeny obtained would express only human λ light chains as described in the foregoing examples. Breeding is performed by standard techniques recognized in the art and, alternatively, by commercial companies, e.g., The Jackson Laboratory. Mouse strains bearing human λ light chain gene segments at the endogenous κ locus and a deletion of the endogenous λ light chain locus are screened for presence of the unique reverse-chimeric (human-mouse) λ light chains and absence of endogenous mouse λ light chains.
[00267] Mice bearing an unrearranged human λ light chain locus are also bred with mice that contain a replacement of the endogenous mouse heavy chain variable gene locus with the human heavy chain variable gene locus (see US 6,596,541 , Regeneron Pharmaceuticals, the VELOCIMMUNE® genetically engineered mouse). The
VELOCIMMUNE® mouse includes, in part, having a genome comprising human heavy chain variable regions operably linked to endogenous mouse constant region loci such that the mouse produces antibodies comprising a human heavy chain variable region and a mouse heavy chain constant region in response to antigenic stimulation. The DNA encoding the variable regions of the heavy chains of the antibodies can be isolated and operably linked to DNA encoding the human heavy chain constant regions. The DNA can then be expressed in a cell capable of expressing the fully human heavy chain of the antibody. Upon a suitable breeding schedule, mice bearing a replacement of the endogenous mouse heavy chain locus with the human heavy chain locus and an unrearranged human λ light chain locus at the endogenous κ light chain locus is obtained. Antibodies containing somatically mutated human heavy chain variable regions and human λ light chain variable regions can be isolated upon immunization with an antigen of interest.
Example VII
Generation of Antibodies From Mice Expressing Human Heavy Chains and Human λ Light Chains
[00268] After breeding mice that contain the unrearranged human λ light chain locus to various desired strains containing modifications and deletions of other endogenous Ig loci (as described above), selected mice are immunized with an antigen of interest.
[00269] Generally, a VELOCIMMUNE® mouse containing one of the single rearranged human germline light chain regions is challenged with an antigen, and lymphatic cells (such as B-cells) are recovered from serum of the animals. The lymphatic cells may be fused with a myeloma cell line to prepare immortal hybridoma cell lines, and such hybridoma cell lines are screened and selected to identify hybridoma cell lines that produce antibodies containing human heavy chain and human λ light chain that are specific to the antigen used for immunization. DNA encoding the variable regions of the heavy chains and the λ light chains may be isolated and linked to desirable isotypic constant regions of the heavy chain and light chain. Due to the presence of the additional hN λ gene segments as compared to the endogenous mouse λ locus, the diversity of the light chain repertoire is dramatically increased and confers higher diversity on the antigen-specific repertoire upon immunization. The resulting cloned antibody sequences may be subsequently produced in a cell, such as a CHO cell. Alternatively, DNA encoding the antigen-specific chimeric antibodies or the variable domains of the light and heavy chains may be isolated directly from antigen-specific lymphocytes (e.g., B cells).
[00270] Initially, high affinity chimeric antibodies are isolated having a human variable region and a mouse constant region. As described above, the antibodies are
characterized and selected for desirable characteristics, including affinity, selectivity, epitope, efc. The mouse constant regions are replaced with a desired human constant region to generate the fully human antibody containing a somatically mutated human heavy chain and a human λ light chain derived from an unrearranged human λ light chain locus of the invention. Suitable human constant regions include, for example wild type or modified lgG1 , lgG2, lgG3, or lgG4.

Claims

We claim:
1. A mouse comprising in its germline, at an endogenous mouse light chain locus, a human λ light chain variable region sequence, wherein the human lambda variable region sequence is expressed in a light chain that comprises a mouse immunoglobulin constant region gene sequence.
2. The mouse of claim 1 , wherein the endogenous mouse light chain locus is a λ locus.
3. The mouse of claim 1 , wherein the endogenous mouse light chain locus is a κ locus.
4. The mouse of claim 1 , wherein the mouse lacks an endogenous light chain variable sequence at the endogenous mouse light chain locus.
5. The mouse of claim 1 , wherein all or substantially all endogenous mouse light chain variable region gene segments are replaced with one or more human λ variable region gene segments.
6. The mouse of claim 1 , wherein the human λ light chain variable region sequence comprises a human ϋλ sequence.
7. The mouse of claim 6, wherein the human ϋλ sequence is selected from the group consisting of ϋλ1 , J 2, ϋλ3, ϋλ7, and a combination thereof.
8. The mouse of claim 1 , wherein the human λ light chain variable region sequence comprises a fragment of cluster A of the human light chain locus.
9. The mouse of claim 8, wherein the fragment of cluster A of the human λ light chain locus extends from Ιι\/λ3-27 through η\/λ3-1.
10. The mouse of claim 1 , wherein the human λ light chain variable region sequence comprises a fragment of cluster B of the human light chain locus.
1 1. The mouse of claim 10, wherein the fragment of cluster B of the human λ light chain locus extends from hV 5-52 through hV 1-40.
12. The mouse of claim 1 , wherein the human λ light chain variable region sequence comprises a genomic fragment of cluster A and a genomic fragment of cluster B.
13. The mouse of claim 12, wherein the human λ light chain variable region sequence comprises at least one gene segment of cluster A and at least one gene segment of cluster B.
14. The mouse of claim 1 , wherein more than 10% of the light chain repertoire of the mouse is derived from at least two hV gene segments selected from 2-8, 2-23, 1-40, 5-45, and 9-49.
15. The mouse of claim 14, wherein more than 20% of the light chain repertoire of the mouse is derived from at least three hN λ gene segments selected from 2-8, 2-23, 1-40, 5-45, and 9-49.
16. The mouse of claim 15, wherein more than 30% of the light chain repertoire of the mouse is derived from at least four hV gene segments selected from 2-8, 2-23, 1 -40, 5-45, and 9-49.
17. A mouse that expresses an immunoglobulin light chain that comprises a human lambda variable sequence fused with a mouse constant region, wherein the mouse exhibits a usage to λ usage ratio of about 1 :1.
18. The mouse of claim 17, wherein the immunoglobulin light chain is expressed from an endogenous mouse light chain locus.
19. Use of a mouse as described in any one of the preceding claims to make an antigen-binding protein.
20. Use according to claim 19, wherein the antigen-binding protein is human.
A cell or tissue derived from a mouse of any one of claims
PCT/US2011/041366 2010-06-22 2011-06-22 Mice expressing alight chain with human lambda variable and mouse constant regions WO2011163311A1 (en)

Priority Applications (41)

Application Number Priority Date Filing Date Title
KR1020227037565A KR20220150430A (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
JP2013516714A JP5988969B2 (en) 2010-06-22 2011-06-22 Mice expressing a light chain comprising a human λ variable region and a mouse constant region
SI201130867A SI2480675T1 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
IL300712A IL300712B1 (en) 2010-06-22 2011-06-22 Human lambda light chain mice
MEP-2016-132A ME02440B (en) 2010-06-22 2011-06-22 Mice expressing alight chain with human lambda variable and mouse constant regions
CN201180038415.2A CN103068994B (en) 2010-06-22 2011-06-22 Express the mouse with the light chain of people λ variable region and murine constant region
KR1020197037332A KR102211911B1 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
ES11728508.0T ES2575223T3 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with the human lambda variable and mouse constant regions
SG2012093258A SG186390A1 (en) 2010-06-22 2011-06-22 Mice expressing alight chain with human lambda variable and mouse constant regions
BR112012033248A BR112012033248A2 (en) 2010-06-22 2011-06-22 mice expressing a light chain with human lip variable and mouse constant regions
LTEP11728508.0T LT2480675T (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
KR1020137001586A KR101945352B1 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
RS20160483A RS54891B1 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
IL313063A IL313063A (en) 2010-06-22 2011-06-22 Human lambda light chain mice
NZ605751A NZ605751A (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
AU2011271043A AU2011271043B8 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
DK11728508.0T DK2480675T3 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with the human lambda variable and constant regions from mouse
EP11728508.0A EP2480675B1 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
KR1020217017823A KR102462042B1 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
MX2015009162A MX347322B (en) 2010-06-22 2011-06-22 Mice expressing alight chain with human lambda variable and mouse constant regions.
CA2804311A CA2804311C (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
KR1020197002870A KR101991234B1 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
MX2012015300A MX336344B (en) 2010-06-22 2011-06-22 Mice expressing alight chain with human lambda variable and mouse constant regions.
KR1020197017074A KR102059909B1 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
KR1020217002982A KR102266097B1 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
RU2013102596/10A RU2590594C2 (en) 2010-06-22 2011-06-22 Mice, expressing light chain with variable region of alpha human and constant area of mouse
KR1020197002903A KR102001430B1 (en) 2010-06-22 2011-06-22 Mice expressing a light chain with human lambda variable and mouse constant regions
HK12111457.9A HK1170766A1 (en) 2010-06-22 2012-11-13 Mice expressing a light chain with human lambda variable and mouse constant regions
IL223719A IL223719A (en) 2010-06-22 2012-12-18 Transgenic mice whose genome comprises an endogenous lambda light chain immunoglobulin locus and methods for cloning a lambda light chain variable region
ZA2013/00063A ZA201300063B (en) 2010-06-22 2013-01-03 Mice expressing alight chain with human lambda variabe and mouse constant regions
AU2015275243A AU2015275243B2 (en) 2010-06-22 2015-12-22 Mice expressing a light chain with human lambda variable and mouse constant regions
IL244450A IL244450A (en) 2010-06-22 2016-03-06 Method for making an antibody comprising a human gamma variable domain
CY20161100585T CY1117692T1 (en) 2010-06-22 2016-06-28 MICES EXPRESSING A LIGHT CHAIN WITH HUMAN VARIABLE LAMB AND CONSTANT MATTER
SM201600213T SMT201600213B (en) 2010-06-22 2016-07-05 MICE EXPRESSING A LIGHT CHAIN INCLUDING A LAMBDA HUMAN VARIABLE REGION AND A CONSTANT MOUSE REGION
HRP20160794TT HRP20160794T1 (en) 2010-06-22 2016-07-06 Mice expressing a light chain with human lambda variable and mouse constant regions
IL255179A IL255179B (en) 2010-06-22 2017-10-22 Mice expressing a light chain with human lambda variable and mouse constant regions
IL259965A IL259965B (en) 2010-06-22 2018-06-12 Mice expressing a light chain with human lambda variable and mouse constant regions
IL264634A IL264634B (en) 2010-06-22 2019-02-04 Mice expressing a light chain with human lambda variable and mouse constant regions
IL269078A IL269078B (en) 2010-06-22 2019-09-02 Mice expressing a light chain with human lambda variable and mouse constant regions
IL282872A IL282872B (en) 2010-06-22 2021-05-03 Human lambda light chain mice
IL291301A IL291301B2 (en) 2010-06-22 2022-03-13 Human lambda light chain mice

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US35731710P 2010-06-22 2010-06-22
US35731410P 2010-06-22 2010-06-22
US61/357,314 2010-06-22
US61/357,317 2010-06-22

Publications (1)

Publication Number Publication Date
WO2011163311A1 true WO2011163311A1 (en) 2011-12-29

Family

ID=44509861

Family Applications (2)

Application Number Title Priority Date Filing Date
PCT/US2011/041366 WO2011163311A1 (en) 2010-06-22 2011-06-22 Mice expressing alight chain with human lambda variable and mouse constant regions
PCT/US2011/041370 WO2011163314A1 (en) 2010-06-22 2011-06-22 Hybrid light chain mice

Family Applications After (1)

Application Number Title Priority Date Filing Date
PCT/US2011/041370 WO2011163314A1 (en) 2010-06-22 2011-06-22 Hybrid light chain mice

Country Status (31)

Country Link
US (22) US9012717B2 (en)
EP (7) EP3034608B1 (en)
JP (15) JP6009441B2 (en)
KR (16) KR101945352B1 (en)
CN (4) CN104404050B (en)
AU (1) AU2011271046B2 (en)
BR (3) BR122020013427B1 (en)
CA (2) CA2803864C (en)
CY (5) CY1117537T1 (en)
DK (5) DK3034608T3 (en)
ES (5) ES2576928T3 (en)
HK (4) HK1168384A1 (en)
HR (5) HRP20160497T1 (en)
HU (5) HUE036597T2 (en)
IL (12) IL300712B1 (en)
LT (4) LT3034608T (en)
ME (5) ME02440B (en)
MX (6) MX347318B (en)
MY (6) MY157477A (en)
NO (1) NO2905338T3 (en)
NZ (6) NZ627119A (en)
PL (5) PL2480675T3 (en)
PT (5) PT3034608T (en)
RS (5) RS56589B1 (en)
RU (3) RU2724736C2 (en)
SG (4) SG10201504568YA (en)
SI (5) SI3034608T1 (en)
SM (3) SMT201600213B (en)
TR (1) TR201905992T4 (en)
WO (2) WO2011163311A1 (en)
ZA (5) ZA201300062B (en)

Cited By (61)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013041845A2 (en) 2011-09-19 2013-03-28 Kymab Limited Animals, repertoires & methods
WO2013061098A2 (en) 2011-12-02 2013-05-02 Kymab Limited Functional isotype switching of chimaeric antibody chains & chimaeric animals expressing different igh isotypes
WO2013096142A1 (en) * 2011-12-20 2013-06-27 Regeneron Pharmaceuticals, Inc. Humanized light chain mice
WO2013144567A1 (en) 2012-03-28 2013-10-03 Kymab Limited Transgenic non-human vertebrate for the expression of class - switched, fully human, antibodies
US20140017238A1 (en) 2001-02-16 2014-01-16 Regeneron Pharmaceuticals, Inc. Methods of Modifying Eukaryotic Cells
EP2757875A2 (en) 2011-09-19 2014-07-30 Kymab Limited Manipulation of immunoglobulin gene diversity and multi-antibody therapeutics
WO2014130690A1 (en) 2013-02-20 2014-08-28 Regeneron Pharmaceuticals, Inc. Non-human animals with modified immunoglobulin heavy chain sequences
EP2798950A1 (en) * 2009-07-08 2014-11-05 Kymab Limited Animal models and therapeutic molecules
US20150033369A1 (en) * 2013-05-02 2015-01-29 Kymab Limited Animals, repertoires & methods
EP2852672A2 (en) * 2012-05-17 2015-04-01 Kymab Limited In vivo guided selection&antibodies
EP2947151A1 (en) * 2010-08-02 2015-11-25 Regeneron Pharmaceuticals, Inc. Binding proteins comprising vl domains
WO2015187835A2 (en) 2014-06-06 2015-12-10 Bristol-Myers Squibb Company Antibodies against glucocorticoid-induced tumor necrosis factor receptor (gitr) and uses thereof
EP2967012A1 (en) 2013-03-14 2016-01-20 Erasmus University Medical Center Rotterdam Transgenic non-human mammal for antibody production
WO2016081748A2 (en) 2014-11-21 2016-05-26 Bristol-Myers Squibb Company Antibodies against cd73 and uses thereof
WO2016097865A1 (en) 2014-12-19 2016-06-23 Regenesance B.V. Antibodies that bind human c6 and uses thereof
US9445581B2 (en) * 2012-03-28 2016-09-20 Kymab Limited Animal models and therapeutic molecules
WO2016196228A1 (en) 2015-05-29 2016-12-08 Bristol-Myers Squibb Company Antibodies against ox40 and uses thereof
WO2017004016A1 (en) 2015-06-29 2017-01-05 The Rockefeller University Antibodies to cd40 with enhanced agonist activity
WO2017087678A2 (en) 2015-11-19 2017-05-26 Bristol-Myers Squibb Company Antibodies against glucocorticoid-induced tumor necrosis factor receptor (gitr) and uses thereof
WO2017152085A1 (en) 2016-03-04 2017-09-08 Bristol-Myers Squibb Company Combination therapy with anti-cd73 antibodies
WO2017151176A1 (en) 2016-03-04 2017-09-08 The Rockefeller University Antibodies to cd40 with enhanced agonist activity
US9783618B2 (en) 2013-05-01 2017-10-10 Kymab Limited Manipulation of immunoglobulin gene diversity and multi-antibody therapeutics
US9783593B2 (en) 2013-05-02 2017-10-10 Kymab Limited Antibodies, variable domains and chains tailored for human use
US9788534B2 (en) 2013-03-18 2017-10-17 Kymab Limited Animal models and therapeutic molecules
US9796788B2 (en) 2010-02-08 2017-10-24 Regeneron Pharmaceuticals, Inc. Mice expressing a limited immunoglobulin light chain repertoire
WO2017196663A1 (en) 2016-05-09 2017-11-16 Bristol-Myers Squibb Company Tl1a antibodies and uses thereof
WO2017214089A1 (en) * 2016-06-06 2017-12-14 Regeneron Pharmaceuticals, Inc. Non-human animals expressing antibodies with human lambda light chains
WO2018013818A2 (en) 2016-07-14 2018-01-18 Bristol-Myers Squibb Company Antibodies against tim3 and uses thereof
WO2018044970A1 (en) 2016-08-31 2018-03-08 University Of Rochester Human monoclonal antibodies to human endogenous retrovirus k envelope (herv-k) and uses thereof
WO2018071822A2 (en) 2016-10-13 2018-04-19 Massachusetts Institute Of Technology Antibodies that bind zika virus envelope protein and uses thereof
US9963716B2 (en) 2011-09-26 2018-05-08 Kymab Limited Chimaeric surrogate light chains (SLC) comprising human VpreB
US9969814B2 (en) 2010-02-08 2018-05-15 Regeneron Pharmaceuticals, Inc. Methods for making fully human bispecific antibodies using a common light chain
WO2018128691A1 (en) * 2016-11-04 2018-07-12 Regeneron Pharmaceuticals, Inc. Non-human animals having an engineered immunoglobulin lambda light chain locus
WO2018151821A1 (en) 2017-02-17 2018-08-23 Bristol-Myers Squibb Company Antibodies to alpha-synuclein and uses thereof
WO2018187613A2 (en) 2017-04-07 2018-10-11 Bristol-Myers Squibb Company Anti-icos agonist antibodies and uses thereof
US10130081B2 (en) 2011-08-05 2018-11-20 Regeneron Pharmaceuticals, Inc. Humanized universal light chain mice
US10143186B2 (en) 2010-02-08 2018-12-04 Regeneron Pharmaceuticals, Inc. Common light chain mouse
US10149462B2 (en) 2013-10-01 2018-12-11 Kymab Limited Animal models and therapeutic molecules
US10251377B2 (en) 2012-03-28 2019-04-09 Kymab Limited Transgenic non-human vertebrate for the expression of class-switched, fully human, antibodies
US10266803B2 (en) 2010-06-22 2019-04-23 Regeneron Pharmaceuticals, Inc. Human lambda light chain mice
US10344299B2 (en) 2000-10-31 2019-07-09 Regeneron Pharmaceuticals, Inc. Compositions and methods for modifying cells
WO2019140229A1 (en) 2018-01-12 2019-07-18 Bristol-Myers Squibb Company Antibodies against tim3 and uses thereof
WO2020102501A1 (en) 2018-11-16 2020-05-22 Bristol-Myers Squibb Company Anti-nkg2a antibodies and uses thereof
US10662256B2 (en) 2010-07-26 2020-05-26 Trianni, Inc. Transgenic mammals and methods of use thereof
WO2020154293A1 (en) 2019-01-22 2020-07-30 Bristol-Myers Squibb Company Antibodies against il-7r alpha subunit and uses thereof
US10787522B2 (en) 2014-03-21 2020-09-29 Regeneron Pharmaceuticals, Inc. VL antigen binding proteins exhibiting distinct binding characteristics
US10793829B2 (en) 2010-07-26 2020-10-06 Trianni, Inc. Transgenic mammals and methods of use thereof
US10813346B2 (en) 2015-12-03 2020-10-27 Trianni, Inc. Enhanced immunoglobulin diversity
JP2020182490A (en) * 2013-03-13 2020-11-12 リジェネロン・ファーマシューティカルズ・インコーポレイテッドＲｅｇｅｎｅｒｏｎ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ， Ｉｎｃ． Mice expressing limited immunoglobulin light chain repertoire
WO2020247623A1 (en) * 2019-06-05 2020-12-10 Regeneron Pharmaceuticals, Inc. Non-human animals having a limited lambda light chain repertoire expressed from the kappa locus and uses thereof
US10881084B2 (en) 2010-07-26 2021-01-05 Trianni, Inc Transgenic animals and methods of use
US10881085B2 (en) 2014-03-21 2021-01-05 Regeneron Pharmaceuticals, Inc. Non-human animals that make single domain binding proteins
WO2021003152A1 (en) * 2019-07-01 2021-01-07 Trianni, Inc. Transgenic mammals and methods of use thereof
US10894818B2 (en) 2014-10-03 2021-01-19 Massachusetts Institute Of Technology Antibodies that bind Ebola glycoprotein and uses thereof
US11053288B2 (en) 2016-02-04 2021-07-06 Trianni, Inc. Enhanced production of immunoglobulins
US11111314B2 (en) 2015-03-19 2021-09-07 Regeneron Pharmaceuticals, Inc. Non-human animals that select for light chain variable regions that bind antigen
WO2021231732A1 (en) 2020-05-15 2021-11-18 Bristol-Myers Squibb Company Antibodies to garp
US11242393B2 (en) 2018-03-23 2022-02-08 Bristol-Myers Squibb Company Antibodies against MICA and/or MICB and uses thereof
EP4249066A2 (en) 2014-12-23 2023-09-27 Bristol-Myers Squibb Company Antibodies to tigit
US11877565B2 (en) 2008-12-18 2024-01-23 Erasmus University Medical Center Antibody production
WO2024163477A1 (en) 2023-01-31 2024-08-08 University Of Rochester Immune checkpoint blockade therapy for treating staphylococcus aureus infections

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LT2346994T (en) 2008-09-30 2022-03-10 Ablexis, Llc Knock-in mice for the production of chimeric antibodies
US9580491B2 (en) 2010-03-31 2017-02-28 Ablexis, Llc Genetic engineering of non-human animals for the production of chimeric antibodies
PT2825037T (en) 2012-03-16 2019-08-07 Regeneron Pharma Rodents expressing ph-sensitive immunoglobulin sequences
HUE053310T2 (en) 2012-03-16 2021-06-28 Regeneron Pharma Histidine engineered light chain antibodies and genetically modified rodents for generating the same
SG10201607727PA (en) 2012-03-16 2016-11-29 Regeneron Pharma Mice that produce antigen-binding proteins with ph-dependent binding characteristics
US20140013456A1 (en) 2012-03-16 2014-01-09 Regeneron Pharmaceuticals, Inc. Histidine Engineered Light Chain Antibodies and Genetically Modified Non-Human Animals for Generating the Same
TR201909967T4 (en) * 2013-09-18 2019-07-22 Regeneron Pharma Histidine-treated light chain antibodies and non-human animals genetically modified to produce it.
US20170101460A1 (en) * 2014-01-10 2017-04-13 Allermabs Co. Ltd. Transgenic animals capable of producing humanized ige at much higher levels than mouse ige
CA2959428A1 (en) 2014-09-19 2016-03-24 Regeneron Pharmaceuticals, Inc. Chimeric antigen receptors
TR201904686T4 (en) 2015-02-05 2019-05-21 Basf Se A SOLAR POWER PLANT WITH A FIRST HEAT TRANSFER CYCLE AND A SECOND HEAT TRANSFER CYCLE
CN105274116B (en) * 2015-10-21 2020-09-29 重庆金迈博生物科技有限公司 Nucleic acid molecule for preparing humanized antibody and application thereof
AU2017268458B2 (en) 2016-05-20 2022-07-21 Regeneron Pharmaceuticals, Inc. Methods for breaking immunological tolerance using multiple guide RNAS
CA3026088A1 (en) 2016-06-03 2017-12-07 Regeneron Pharmaceuticals, Inc. Non-human animals expressing exogenous terminal deoxynucleotidyltransferase
US20170371963A1 (en) * 2016-06-27 2017-12-28 Facebook, Inc. Systems and methods for identifying matching content
JP6868250B2 (en) 2016-10-31 2021-05-12 国立大学法人鳥取大学 Human antibody-producing non-human animals and human antibody production methods using them
JP7430636B2 (en) 2017-12-05 2024-02-13 リジェネロン・ファーマシューティカルズ・インコーポレイテッド Non-human animals with engineered immunoglobulin lambda light chains and uses thereof
WO2019190922A1 (en) 2018-03-24 2019-10-03 Regeneron Pharmaceuticals, Inc. Genetically modified non-human animals for generating therapeutic antibodies against peptide-mhc complexes, methods of making and uses thereof
JP7328243B2 (en) 2018-03-26 2023-08-16 リジェネロン・ファーマシューティカルズ・インコーポレイテッド Humanized rodents for testing therapeutic agents
KR102480493B1 (en) * 2018-06-08 2022-12-21 크리스탈 바이오사이언스 주식회사 Transgenic animals to produce different antibodies with the same light chain I
IL305557A (en) 2018-06-14 2023-10-01 Regeneron Pharma Non-human animals capable of engineered dh-dh rearrangement and uses thereof
CN112969929B (en) 2018-10-26 2024-06-21 日本汽车能源株式会社 Battery control device
BR112021016173A2 (en) 2019-02-22 2021-11-03 Regeneron Pharma Genetically modified rodent, methods of producing a genetically modified rodent and producing an anti-nav1.7 antibody, isolated rodent cell or tissue, immortalized cell line, rodent embryo, targeting nucleic acid construct, and, hybridoma
JP2023504172A (en) 2019-12-02 2023-02-01 リジェネロン・ファーマシューティカルズ・インコーポレイテッド Peptide-MHC II protein constructs and their uses
CN115988960A (en) * 2020-06-25 2023-04-18 株式会社湖美宝 Hybrid transgenic animals
EP4211155A1 (en) 2020-09-11 2023-07-19 Regeneron Pharmaceuticals, Inc. Identification and production of antigen-specific antibodies
IL303626A (en) 2020-12-16 2023-08-01 Regeneron Pharma Mice expressing humanized fc alpha receptors
US20240317849A1 (en) 2020-12-23 2024-09-26 Regeneron Pharmaceuticals, Inc. Nucleic acids encoding anchor modified antibodies and uses thereof
BR112023011689A2 (en) 2020-12-23 2023-10-31 Regeneron Pharma METHOD FOR OBTAINING AN ANTIBODY PRODUCING CELL, ANTIBODY, AND MAMMALIAN HOST CELL

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000026373A1 (en) 1998-11-03 2000-05-11 Babraham Institute MURINE EXPRESSION OF HUMAN Igμ LOCUS
US20020026036A1 (en) 1991-09-18 2002-02-28 Kyowa Hakko Kogyo Co., Ltd. Process for producing humanized chimera antibody
US6586251B2 (en) 2000-10-31 2003-07-01 Regeneron Pharmaceuticals, Inc. Methods of modifying eukaryotic cells
US6596541B2 (en) 2000-10-31 2003-07-22 Regeneron Pharmaceuticals, Inc. Methods of modifying eukaryotic cells
US20030217373A1 (en) 2001-11-30 2003-11-20 Green Larry L. Transgenic animals bearing human Ig-lambda light chain genes
US6774279B2 (en) 1997-05-30 2004-08-10 Carnegie Institution Of Washington Use of FLP recombinase in mice
US20060015957A1 (en) 1991-08-28 2006-01-19 Genpharm International, Inc. Transgenic non-human animals for producing chimeric antibodies
US7294754B2 (en) 2004-10-19 2007-11-13 Regeneron Pharmaceuticals, Inc. Method for generating an animal homozygous for a genetic modification
WO2008054606A2 (en) 2006-10-02 2008-05-08 Regeneron Pharmaceuticals, Inc. High affinity human antibodies to human il-4 receptor
WO2009043472A2 (en) 2007-09-26 2009-04-09 Carl Zeiss Microimaging Gmbh Method for the microscopic three-dimensional reproduction of a sample
WO2009143472A2 (en) * 2008-05-23 2009-11-26 Aliva Biopharmaceuticals, Inc. Method of generating single vl domain antibodies in transgenic animals

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8823869D0 (en) * 1988-10-12 1988-11-16 Medical Res Council Production of antibodies
US6673986B1 (en) 1990-01-12 2004-01-06 Abgenix, Inc. Generation of xenogeneic antibodies
US5770429A (en) * 1990-08-29 1998-06-23 Genpharm International, Inc. Transgenic non-human animals capable of producing heterologous antibodies
ES2315612T3 (en) 1991-04-10 2009-04-01 The Scripps Research Institute GENOTECAS OF HETERODYMERIC RECEPTORS USING PHAGEMIDS.
IL109168A0 (en) * 1993-04-01 1994-06-24 Univ Columbia A retroviral vector capable of transducing the aldehyde dehydrogenase-1 gene and making cells resistant to the chemotherapeutic agent cyclophosphamide and its derivatives and analogs
US6632976B1 (en) 1995-08-29 2003-10-14 Kirin Beer Kabushiki Kaisha Chimeric mice that are produced by microcell mediated chromosome transfer and that retain a human antibody gene
KR20080059467A (en) * 1996-12-03 2008-06-27 아브게닉스, 인크. Transgenic mammals having human ig loci including plural vh and vk regions and antibodies produced therefrom
CN101498731A (en) * 2000-05-18 2009-08-05 日本烟草产业株式会社 Human monoclonal antibody against a costimulatory signal transduction molecule ATLIM and pharmaceutical use thereof
PT1354034E (en) * 2000-11-30 2008-02-28 Medarex Inc Transgenic transchromosomal rodents for making human antibodies
GB0031284D0 (en) * 2000-12-21 2001-01-31 Ks Biomedix Ltd High affinity antibodies
DE60227067D1 (en) * 2001-05-11 2008-07-24 Kirin Pharma Kk ARTIFICIAL HUMAN CHROMOSOME WITH THE GENE FOR THE LAMBDA LIGHT CHAIN OF HUMAN ANTIBODIES
GB0115256D0 (en) * 2001-06-21 2001-08-15 Babraham Inst Mouse light chain locus
US20030217171A1 (en) 2002-05-17 2003-11-20 Von Stuermer Wolfgang R. Self-replicating and self-installing software apparatus
MXPA06000562A (en) * 2003-07-15 2006-03-30 Therapeutic Human Polyclonals Humanized immunoglobulin loci.
CN1605628A (en) * 2003-09-03 2005-04-13 中国疾病预防控制中心病毒病预防控制所 Human source anti-hepatitis A virus gene engineering antibody from CHO cell
RU2398777C2 (en) * 2004-08-05 2010-09-10 Дженентек, Инк. HUMANISED ANTI c-met ANTAGONISTS
ES2359567T3 (en) * 2004-12-29 2011-05-24 Yuhan Corporation SPECIFIC HUMANIZED ANTIBODY FOR THE TUMORAL-ALFA NECROSIS FACTOR.
EP2505058A1 (en) 2006-03-31 2012-10-03 Medarex, Inc. Transgenic animals expressing chimeric antibodies for use in preparing human antibodies
JP2010501165A (en) * 2006-08-22 2010-01-21 ジーツー インフラメイション プロプライエタリー リミテッド Antibody production method
US7864492B2 (en) 2006-10-31 2011-01-04 Siemens Industry, Inc. Systems and methods for arc fault detection
US8012714B2 (en) * 2008-04-14 2011-09-06 Innovative Targeting Solutions, Inc. Sequence diversity generation in immunoglobulins
LT2346994T (en) 2008-09-30 2022-03-10 Ablexis, Llc Knock-in mice for the production of chimeric antibodies
RU2011129459A (en) * 2008-12-18 2013-01-27 Эрасмус Юниверсити Медикал Сентр Роттердам TRANSGENIC ANIMALS (NOT HUMAN), EXPRESSING HUMANIZED ANTIBODIES, AND THEIR APPLICATION
CN102638971B (en) * 2009-07-08 2015-10-07 科马布有限公司 Animal model and treatment molecule
RU2724663C2 (en) * 2010-02-08 2020-06-25 Ридженерон Фармасьютикалз, Инк. Mouse with common light chain
CN103228130B (en) 2010-06-17 2016-03-16 科马布有限公司 Animal model and treatment molecule
JP6009441B2 (en) * 2010-06-22 2016-10-19 リジェネロン・ファーマシューティカルズ・インコーポレイテッドＲｅｇｅｎｅｒｏｎ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ， Ｉｎｃ． Hybrid light chain mouse

Patent Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060015957A1 (en) 1991-08-28 2006-01-19 Genpharm International, Inc. Transgenic non-human animals for producing chimeric antibodies
US20020026036A1 (en) 1991-09-18 2002-02-28 Kyowa Hakko Kogyo Co., Ltd. Process for producing humanized chimera antibody
US6774279B2 (en) 1997-05-30 2004-08-10 Carnegie Institution Of Washington Use of FLP recombinase in mice
US6998514B2 (en) 1998-11-03 2006-02-14 Babraham Institute Murine expression of a human IgA lambda locus
WO2000026373A1 (en) 1998-11-03 2000-05-11 Babraham Institute MURINE EXPRESSION OF HUMAN Igμ LOCUS
US6596541B2 (en) 2000-10-31 2003-07-22 Regeneron Pharmaceuticals, Inc. Methods of modifying eukaryotic cells
US6586251B2 (en) 2000-10-31 2003-07-01 Regeneron Pharmaceuticals, Inc. Methods of modifying eukaryotic cells
US20030217373A1 (en) 2001-11-30 2003-11-20 Green Larry L. Transgenic animals bearing human Ig-lambda light chain genes
US7435871B2 (en) 2001-11-30 2008-10-14 Amgen Fremont Inc. Transgenic animals bearing human Igλ light chain genes
US7294754B2 (en) 2004-10-19 2007-11-13 Regeneron Pharmaceuticals, Inc. Method for generating an animal homozygous for a genetic modification
WO2008054606A2 (en) 2006-10-02 2008-05-08 Regeneron Pharmaceuticals, Inc. High affinity human antibodies to human il-4 receptor
US7605237B2 (en) 2006-10-02 2009-10-20 Regeneron Pharmaceuticals, Inc. High affinity human antibodies to human IL-4 receptor
WO2009043472A2 (en) 2007-09-26 2009-04-09 Carl Zeiss Microimaging Gmbh Method for the microscopic three-dimensional reproduction of a sample
WO2009143472A2 (en) * 2008-05-23 2009-11-26 Aliva Biopharmaceuticals, Inc. Method of generating single vl domain antibodies in transgenic animals

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
GORMAN ET AL., IMMUNITY, vol. 5, no. 3, 1996, pages 241 - 252
GORMAN J R ET AL: "THE LGK 3' ENHANCER INFLUENCES THE RATIO OF LGK VERSUS LGL B LYMPHOCYTES", IMMUNITY, CELL PRESS, US, vol. 5, no. 3, 1 September 1996 (1996-09-01), pages 241 - 252, XP000891305, ISSN: 1074-7613, DOI: 10.1016/S1074-7613(00)80319-2 *
POPOV A V ET AL: "A HUMAN IMMUNOGLOBULIN L LOCUS IS SIMILARLY WELL EXPRESSED IN MICE AND HUMANS", THE JOURNAL OF EXPERIMENTAL MEDICINE, ROCKEFELLER UNIVERSITY PRESS, US, vol. 189, no. 10, 17 May 1999 (1999-05-17), pages 1611 - 1619, XP000891331, ISSN: 0022-1007, DOI: 10.1084/JEM.189.10.1611 *
POPOV ET AL., J EXP MED, vol. 189, no. 10, 1999, pages 1611 - 1619
POUEYMIROU ET AL.: "FO generation mice that are essentially fully derived from the donor gene-targeted ES cells allowing immediate phenotypic analyses", NATURE BIOTECH., vol. 25, no. 1, 2007, pages 91 - 99
VALENZUELA ET AL.: "High-throughput engineering of the mouse genome coupled with high-resolution expression analysis", NATURE BIOTECH., vol. 21, no. 6, 2003, pages 652 - 659

Cited By (167)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10344299B2 (en) 2000-10-31 2019-07-09 Regeneron Pharmaceuticals, Inc. Compositions and methods for modifying cells
US9376699B2 (en) 2000-10-31 2016-06-28 Regeneron Pharmaceuticals, Inc. Methods of producing hybrid antibodies
US9708635B2 (en) 2000-10-31 2017-07-18 Regeneron Pharmaceuticals, Inc. Methods of making a nucleic acid encoding a human variable region
US10227625B2 (en) 2000-10-31 2019-03-12 Regeneron Pharmaceuticals, Inc. Methods of modifying eukaryotic cells
US10584364B2 (en) 2000-12-07 2020-03-10 Rgeneron Pharmaceuticals, Inc. Mice that produce hybrid antibodies
US10378037B2 (en) 2001-02-16 2019-08-13 Regeneron Pharmaceuticals, Inc. Methods of making a nucleic acid encoding a human variable region
US20140017238A1 (en) 2001-02-16 2014-01-16 Regeneron Pharmaceuticals, Inc. Methods of Modifying Eukaryotic Cells
US10378039B2 (en) 2001-02-16 2019-08-13 Regeneron Pharmaceuticals, Inc. Mouse embryonic stem cells comprising a hybrid heavy chain immunoglobulin locus
US10378038B2 (en) 2001-02-16 2019-08-13 Regeneron Pharmaceuticals, Inc. Mice that produce hybrid antibodies
US10378040B2 (en) 2001-02-16 2019-08-13 Regeneron Pharmaceuticals, Inc. Mice that produce hybrid antibodies
US9353394B2 (en) 2001-02-16 2016-05-31 Regeneron Pharmaceuticals, Inc. Methods of producing hybrid antibodies
US10526630B2 (en) 2001-02-16 2020-01-07 Regeneron Pharmaceuticals, Inc. Genetically modified mice that produce hybrid antibodies
US9528136B2 (en) 2001-02-16 2016-12-27 Regeneron Pharmaceuticals, Inc. Methods of modifying eukaryotic cells
US9388446B2 (en) 2001-02-16 2016-07-12 Regeneron Pharmaceuticals, Inc. Methods of producing hybrid antibodies
US10640800B2 (en) 2001-02-16 2020-05-05 Regeneron Pharmaceuticals, Inc. Mice that produce hybrid antibodies
US9371553B2 (en) 2001-02-16 2016-06-21 Regeneron Pharmaceuticals, Inc. Genetically modified mice that produce hybrid antibodies
US11877565B2 (en) 2008-12-18 2024-01-23 Erasmus University Medical Center Antibody production
US9434782B2 (en) 2009-07-08 2016-09-06 Kymab Limited Animal models and therapeutic molecules
US10165763B2 (en) 2009-07-08 2019-01-01 Kymab Limited Animal models and therapeutic molecules
EP2798950A1 (en) * 2009-07-08 2014-11-05 Kymab Limited Animal models and therapeutic molecules
US9505827B2 (en) 2009-07-08 2016-11-29 Kymab Limited Animal models and therapeutic molecules
US9504236B2 (en) 2009-07-08 2016-11-29 Kymab Limited Animal models and therapeutic molecules
US11812731B2 (en) 2009-07-08 2023-11-14 Kymab Ltd. Animal models and therapeutic molecules
US11606941B2 (en) 2009-07-08 2023-03-21 Kymab Limited Animal models and therapeutic molecules
US9447177B2 (en) 2009-07-08 2016-09-20 Kymab Limited Transgenic mouse homozygous for chimeric IgH locus
US10064398B2 (en) 2009-07-08 2018-09-04 Kymab Limited Animal models and therapeutic molecules
US9796788B2 (en) 2010-02-08 2017-10-24 Regeneron Pharmaceuticals, Inc. Mice expressing a limited immunoglobulin light chain repertoire
US10143186B2 (en) 2010-02-08 2018-12-04 Regeneron Pharmaceuticals, Inc. Common light chain mouse
US9969814B2 (en) 2010-02-08 2018-05-15 Regeneron Pharmaceuticals, Inc. Methods for making fully human bispecific antibodies using a common light chain
US10167344B2 (en) 2010-02-08 2019-01-01 Regeneron Pharmaceuticals, Inc. Mice expressing a limited immunoglobulin light chain repertoire
US11026407B2 (en) 2010-02-08 2021-06-08 Regeneran Pharmaceuticals, Inc. Mice expressing a limited immunoglobulin light chain repertoire
US10412940B2 (en) 2010-02-08 2019-09-17 Regeneron Pharmaceuticals, Inc. Mice expressing a limited immunoglobulin light chain repertoire
US10986820B2 (en) 2010-02-08 2021-04-27 Regeneron Pharmaceuticals, Inc. Common light chain mouse
US10266803B2 (en) 2010-06-22 2019-04-23 Regeneron Pharmaceuticals, Inc. Human lambda light chain mice
US10881084B2 (en) 2010-07-26 2021-01-05 Trianni, Inc Transgenic animals and methods of use
US12096753B2 (en) 2010-07-26 2024-09-24 Trianni, Inc. Transgenic animals and methods of use
US10793829B2 (en) 2010-07-26 2020-10-06 Trianni, Inc. Transgenic mammals and methods of use thereof
US10662256B2 (en) 2010-07-26 2020-05-26 Trianni, Inc. Transgenic mammals and methods of use thereof
US12049516B2 (en) 2010-07-26 2024-07-30 Trianni, Inc. Transgenic mammals and methods of use thereof
US9686970B2 (en) 2010-08-02 2017-06-27 Regeneron Pharmaceuticals, Inc. Mice that make VL binding proteins
US9516868B2 (en) 2010-08-02 2016-12-13 Regeneron Pharmaceuticals, Inc. Mice that make VL binding proteins
US10954310B2 (en) 2010-08-02 2021-03-23 Regeneran Pharmaceuticals, Inc. Mice that make VL binding proteins
EP3960865A1 (en) * 2010-08-02 2022-03-02 Regeneron Pharmaceuticals, Inc. Mice that make binding proteins comprising vl domains
EP2601298B1 (en) * 2010-08-02 2016-11-30 Regeneron Pharmaceuticals, Inc. Mice that make binding proteins comprising vl domains
EP2947151A1 (en) * 2010-08-02 2015-11-25 Regeneron Pharmaceuticals, Inc. Binding proteins comprising vl domains
US11357217B2 (en) 2011-08-05 2022-06-14 Regeneron Pharmaceuticals, Inc. Humanized universal light chain mice
US10130081B2 (en) 2011-08-05 2018-11-20 Regeneron Pharmaceuticals, Inc. Humanized universal light chain mice
EP2758534B1 (en) 2011-09-19 2020-04-29 Kymab Limited Animals, repertoires & methods for the production of human antibodies
EP2758534A2 (en) 2011-09-19 2014-07-30 Kymab Limited Animals, repertoires & methods for the production of human antibodies
WO2013041845A2 (en) 2011-09-19 2013-03-28 Kymab Limited Animals, repertoires & methods
JP2014531452A (en) * 2011-09-19 2014-11-27 カイマブ・リミテッド Animals, repertoire and methods
EP2757875B1 (en) 2011-09-19 2017-11-29 Kymab Limited Manipulation of immunoglobulin gene diversity and multi-antibody therapeutics
JP2017213005A (en) * 2011-09-19 2017-12-07 カイマブ・リミテッド Animal, repertoire and method
EP3741862A1 (en) 2011-09-19 2020-11-25 Kymab Limited Animals, repertoires & methods for the production of human antibodies
EP2758535A2 (en) 2011-09-19 2014-07-30 Kymab Limited Antibodies, variable domains&chains tailored for human use
EP2757875A2 (en) 2011-09-19 2014-07-30 Kymab Limited Manipulation of immunoglobulin gene diversity and multi-antibody therapeutics
US11051497B2 (en) 2011-09-19 2021-07-06 Kymab Limited Manipulation of immunoglobulin gene diversity and multi-antibody therapeutics
EP3311661B1 (en) 2011-09-19 2022-04-20 Kymab Limited Manipulation of immunoglobulin gene diversity and multi-antibody therapeutics
US9963716B2 (en) 2011-09-26 2018-05-08 Kymab Limited Chimaeric surrogate light chains (SLC) comprising human VpreB
WO2013061098A2 (en) 2011-12-02 2013-05-02 Kymab Limited Functional isotype switching of chimaeric antibody chains & chimaeric animals expressing different igh isotypes
EP2785845A2 (en) * 2011-12-02 2014-10-08 Kymab Limited Functional isotype switching of chimaeric antibody chains & chimaeric animals expressing different igh isotypes
US10561124B2 (en) 2011-12-20 2020-02-18 Regeneron Pharmaceuticals, Inc. Humanized light chain mice
US11612151B2 (en) 2011-12-20 2023-03-28 Regeneron Pharmaceuticals, Inc. Humanized light chain mice
JP2015502177A (en) * 2011-12-20 2015-01-22 リジェネロン・ファーマシューティカルズ・インコーポレイテッドＲｅｇｅｎｅｒｏｎ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ， Ｉｎｃ． Humanized light chain mouse
US11617357B2 (en) 2011-12-20 2023-04-04 Regeneron Pharmaceuticals, Inc. Humanized light chain mice
EP3527070A1 (en) * 2011-12-20 2019-08-21 Regeneron Pharmaceuticals, Inc. Humanized light chain mice
WO2013096142A1 (en) * 2011-12-20 2013-06-27 Regeneron Pharmaceuticals, Inc. Humanized light chain mice
US9706759B2 (en) 2011-12-20 2017-07-18 Regeneron Pharmaceuticals, Inc. Humanized light chain mice
US9622459B2 (en) 2011-12-20 2017-04-18 Regeneron Pharmaceuticals, Inc. Humanized light chain mice
AU2013239501B2 (en) * 2012-03-28 2018-08-02 Kymab Limited Animals expressing human lambda immunoglobulin light chain variable domain
US10774155B2 (en) 2012-03-28 2020-09-15 Kymab Limited Animal models and therapeutic molecules
US9253965B2 (en) * 2012-03-28 2016-02-09 Kymab Limited Animal models and therapeutic molecules
EP2831244A2 (en) 2012-03-28 2015-02-04 Kymab Limited Animal models and therapeutic molecules
CN104334732A (en) * 2012-03-28 2015-02-04 科马布有限公司 Animals expressing human lambda immunoglobulin light chain variable domain
US9445581B2 (en) * 2012-03-28 2016-09-20 Kymab Limited Animal models and therapeutic molecules
EP3366126B1 (en) * 2012-03-28 2024-05-15 Kymab Limited Transgenic mice expressing human lambda immunoglobulin light chain variable domains
US9938358B2 (en) 2012-03-28 2018-04-10 Kymab Limited Animal models and therapeutic molecules
US11297811B2 (en) 2012-03-28 2022-04-12 Kymab Limited Transgenic non-human vertebrate for the expression of class-switched, fully human, antibodies
WO2013144566A2 (en) 2012-03-28 2013-10-03 Kymab Limited Animal models and therapeutic molecules
US10251377B2 (en) 2012-03-28 2019-04-09 Kymab Limited Transgenic non-human vertebrate for the expression of class-switched, fully human, antibodies
US9938357B2 (en) 2012-03-28 2018-04-10 Kymab Limited Animal models and therapeutic molecules
WO2013144567A1 (en) 2012-03-28 2013-10-03 Kymab Limited Transgenic non-human vertebrate for the expression of class - switched, fully human, antibodies
CN104334732B (en) * 2012-03-28 2018-03-30 科马布有限公司 Express the animal of people's lambda immunoglobulin light variable domains
US9924705B2 (en) 2012-03-28 2018-03-27 Kymab Limited Animal models and therapeutic molecules
US9896516B2 (en) 2012-03-28 2018-02-20 Kymab Limited Animal models and therapeutic molecules
WO2013144566A3 (en) * 2012-03-28 2013-11-21 Kymab Limited Animals expressing human lambda immunoglobulin light chain variable domain
EP4116427A1 (en) 2012-05-17 2023-01-11 Kymab Limited In vivo guided selection & antibodies
US10667501B2 (en) 2012-05-17 2020-06-02 Kymab Limited Transgenic non-human vertebrate for the in vivo production of dual specificity immunoglobulins or hypermutated heavy chain only immunoglobulins
EP2852672A2 (en) * 2012-05-17 2015-04-01 Kymab Limited In vivo guided selection&antibodies
EP3351095A1 (en) 2013-02-20 2018-07-25 Regeneron Pharmaceuticals, Inc. Non-human animals with modified immunoglobulin heavy chain sequences
WO2014130690A1 (en) 2013-02-20 2014-08-28 Regeneron Pharmaceuticals, Inc. Non-human animals with modified immunoglobulin heavy chain sequences
JP2020182490A (en) * 2013-03-13 2020-11-12 リジェネロン・ファーマシューティカルズ・インコーポレイテッドＲｅｇｅｎｅｒｏｎ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ， Ｉｎｃ． Mice expressing limited immunoglobulin light chain repertoire
EP2967012A1 (en) 2013-03-14 2016-01-20 Erasmus University Medical Center Rotterdam Transgenic non-human mammal for antibody production
EP2967012B1 (en) * 2013-03-14 2020-09-16 Erasmus University Medical Center Rotterdam Transgenic non-human mammal for antibody production
US9980470B2 (en) 2013-03-14 2018-05-29 Erasmus University Medical Center Antibody production
US9788534B2 (en) 2013-03-18 2017-10-17 Kymab Limited Animal models and therapeutic molecules
US11297810B2 (en) 2013-03-18 2022-04-12 Kymab Limited Animal models and therapeutic molecules
US10226033B2 (en) 2013-03-18 2019-03-12 Kymab Limited Animal models and therapeutic molecules
US9783618B2 (en) 2013-05-01 2017-10-10 Kymab Limited Manipulation of immunoglobulin gene diversity and multi-antibody therapeutics
US9783593B2 (en) 2013-05-02 2017-10-10 Kymab Limited Antibodies, variable domains and chains tailored for human use
US20150033369A1 (en) * 2013-05-02 2015-01-29 Kymab Limited Animals, repertoires & methods
US11707056B2 (en) * 2013-05-02 2023-07-25 Kymab Limited Animals, repertoires and methods
US10730930B2 (en) 2013-05-02 2020-08-04 Kymab Limited Antibodies, variable domains and chains tailored for human use
US11820810B2 (en) 2013-05-02 2023-11-21 Kymab Limited Antibodies, variable domains and chains tailored for human use
US10149462B2 (en) 2013-10-01 2018-12-11 Kymab Limited Animal models and therapeutic molecules
US11399522B2 (en) 2013-10-01 2022-08-02 Kymab Limited Animal models and therapeutic molecules
US10787522B2 (en) 2014-03-21 2020-09-29 Regeneron Pharmaceuticals, Inc. VL antigen binding proteins exhibiting distinct binding characteristics
US10881085B2 (en) 2014-03-21 2021-01-05 Regeneron Pharmaceuticals, Inc. Non-human animals that make single domain binding proteins
EP3610924A1 (en) 2014-06-06 2020-02-19 Bristol-Myers Squibb Company Antibodies against glucocorticoid-induced tumor necrosis factor receptor (gitr) and uses thereof
EP3998079A1 (en) 2014-06-06 2022-05-18 Bristol-Myers Squibb Company Antibodies against glucocorticoid-induced tumor necrosis factor receptor (gitr) and uses thereof
WO2015187835A2 (en) 2014-06-06 2015-12-10 Bristol-Myers Squibb Company Antibodies against glucocorticoid-induced tumor necrosis factor receptor (gitr) and uses thereof
US10894818B2 (en) 2014-10-03 2021-01-19 Massachusetts Institute Of Technology Antibodies that bind Ebola glycoprotein and uses thereof
EP3725808A1 (en) 2014-11-21 2020-10-21 Bristol-Myers Squibb Company Antibodies against cd73 and uses thereof
WO2016081748A2 (en) 2014-11-21 2016-05-26 Bristol-Myers Squibb Company Antibodies against cd73 and uses thereof
WO2016097865A1 (en) 2014-12-19 2016-06-23 Regenesance B.V. Antibodies that bind human c6 and uses thereof
EP3945096A1 (en) 2014-12-19 2022-02-02 Regenesance B.V. Antibodies that bind human c6 and uses thereof
EP4249066A2 (en) 2014-12-23 2023-09-27 Bristol-Myers Squibb Company Antibodies to tigit
US11111314B2 (en) 2015-03-19 2021-09-07 Regeneron Pharmaceuticals, Inc. Non-human animals that select for light chain variable regions that bind antigen
WO2016196228A1 (en) 2015-05-29 2016-12-08 Bristol-Myers Squibb Company Antibodies against ox40 and uses thereof
WO2017004016A1 (en) 2015-06-29 2017-01-05 The Rockefeller University Antibodies to cd40 with enhanced agonist activity
WO2017087678A2 (en) 2015-11-19 2017-05-26 Bristol-Myers Squibb Company Antibodies against glucocorticoid-induced tumor necrosis factor receptor (gitr) and uses thereof
US11889821B2 (en) 2015-12-03 2024-02-06 Trianni, Inc. Enhanced immunoglobulin diversity
US10813346B2 (en) 2015-12-03 2020-10-27 Trianni, Inc. Enhanced immunoglobulin diversity
US11053288B2 (en) 2016-02-04 2021-07-06 Trianni, Inc. Enhanced production of immunoglobulins
EP4406550A2 (en) 2016-03-04 2024-07-31 The Rockefeller University Antibodies to cd40 with enhanced agonist activity
WO2017151176A1 (en) 2016-03-04 2017-09-08 The Rockefeller University Antibodies to cd40 with enhanced agonist activity
WO2017152085A1 (en) 2016-03-04 2017-09-08 Bristol-Myers Squibb Company Combination therapy with anti-cd73 antibodies
WO2017196663A1 (en) 2016-05-09 2017-11-16 Bristol-Myers Squibb Company Tl1a antibodies and uses thereof
US11767364B2 (en) 2016-05-09 2023-09-26 Bristol-Myers Squibb Company TL1A antibodies and methods of treatment
US10968279B2 (en) 2016-05-09 2021-04-06 Bristol-Myers Squibb Company TL1A antibodies and uses thereof
WO2017214089A1 (en) * 2016-06-06 2017-12-14 Regeneron Pharmaceuticals, Inc. Non-human animals expressing antibodies with human lambda light chains
WO2018013818A2 (en) 2016-07-14 2018-01-18 Bristol-Myers Squibb Company Antibodies against tim3 and uses thereof
US11591392B2 (en) 2016-07-14 2023-02-28 Bristol-Myers Squibb Company Antibodies against TIM3 and uses thereof
US10533052B2 (en) 2016-07-14 2020-01-14 Bristol-Myers Squibb Company Antibodies against TIM3 and uses thereof
US10077306B2 (en) 2016-07-14 2018-09-18 Bristol-Myers Squibb Company Antibodies against TIM3 and uses thereof
WO2018044970A1 (en) 2016-08-31 2018-03-08 University Of Rochester Human monoclonal antibodies to human endogenous retrovirus k envelope (herv-k) and uses thereof
WO2018071822A2 (en) 2016-10-13 2018-04-19 Massachusetts Institute Of Technology Antibodies that bind zika virus envelope protein and uses thereof
RU2757665C2 (en) * 2016-11-04 2021-10-20 Регенерон Фармасьютикалс, Инк. Animals other than humans with constructed locus of light lambda chain of immunoglobulin
IL266282B1 (en) * 2016-11-04 2023-12-01 Regeneron Pharma Non-human animals having an engineered immunoglobulin lambda light chain locus
JP2022130725A (en) * 2016-11-04 2022-09-06 リジェネロン・ファーマシューティカルズ・インコーポレイテッド Non-human animals having engineered immunoglobulin lambda light chain locus
EP4082334A1 (en) * 2016-11-04 2022-11-02 Regeneron Pharmaceuticals, Inc. Non-human animals having an engineered immunoglobulin lambda light chain locus
KR20190076024A (en) * 2016-11-04 2019-07-01 리제너론 파마슈티칼스 인코포레이티드 Non-human animal with engineered immunoglobulin lambda light chain locus
KR102492433B1 (en) 2016-11-04 2023-01-30 리제너론 파마슈티칼스 인코포레이티드 Non-human animals having an engineered immunoglobulin lambda light chain locus
KR20230020550A (en) * 2016-11-04 2023-02-10 리제너론 파마슈티칼스 인코포레이티드 Non-human animals having an engineered immunoglobulin lambda light chain locus
JP2020501516A (en) * 2016-11-04 2020-01-23 リジェネロン・ファーマシューティカルズ・インコーポレイテッドＲｅｇｅｎｅｒｏｎ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ， Ｉｎｃ． Non-human animals with engineered immunoglobulin lambda light chain loci
WO2018128691A1 (en) * 2016-11-04 2018-07-12 Regeneron Pharmaceuticals, Inc. Non-human animals having an engineered immunoglobulin lambda light chain locus
AU2017391167B2 (en) * 2016-11-04 2024-02-15 Regeneron Pharmaceuticals, Inc. Non-human animals having an engineered immunoglobulin lambda light chain locus
IL266282B2 (en) * 2016-11-04 2024-04-01 Regeneron Pharma Non-human animals having an engineered immunoglobulin lambda light chain locus
KR102658529B1 (en) 2016-11-04 2024-04-19 리제너론 파마슈티칼스 인코포레이티드 Non-human animals having an engineered immunoglobulin lambda light chain locus
KR20210134059A (en) * 2016-11-04 2021-11-08 리제너론 파마슈티칼스 인코포레이티드 Non-human animals having an engineered immunoglobulin lambda light chain locus
KR102319069B1 (en) 2016-11-04 2021-11-01 리제너론 파마슈티칼스 인코포레이티드 Non-Human Animals With Engineered Immunoglobulin Lambda Light Chain Locus
JP7386292B2 (en) 2016-11-04 2023-11-24 リジェネロン・ファーマシューティカルズ・インコーポレイテッド Non-human animals with engineered immunoglobulin lambda light chain loci
US10820582B2 (en) 2016-11-04 2020-11-03 Regeneron Pharmaceuticals, Inc. Non-human animals having an engineered immunoglobulin Λ light chain locus
US11827695B2 (en) 2017-02-17 2023-11-28 Bristol-Myers Squibb Company Antibodies to alpha-synuclein and uses thereof
WO2018151821A1 (en) 2017-02-17 2018-08-23 Bristol-Myers Squibb Company Antibodies to alpha-synuclein and uses thereof
US11142570B2 (en) 2017-02-17 2021-10-12 Bristol-Myers Squibb Company Antibodies to alpha-synuclein and uses thereof
WO2018187613A2 (en) 2017-04-07 2018-10-11 Bristol-Myers Squibb Company Anti-icos agonist antibodies and uses thereof
WO2019140229A1 (en) 2018-01-12 2019-07-18 Bristol-Myers Squibb Company Antibodies against tim3 and uses thereof
US11242393B2 (en) 2018-03-23 2022-02-08 Bristol-Myers Squibb Company Antibodies against MICA and/or MICB and uses thereof
WO2020102501A1 (en) 2018-11-16 2020-05-22 Bristol-Myers Squibb Company Anti-nkg2a antibodies and uses thereof
WO2020154293A1 (en) 2019-01-22 2020-07-30 Bristol-Myers Squibb Company Antibodies against il-7r alpha subunit and uses thereof
US11919962B2 (en) 2019-01-22 2024-03-05 Bristol Myers-Squibb Company Antibodies against IL-7R alpha subunit and uses thereof
US11008395B2 (en) 2019-01-22 2021-05-18 Bristol Myers-Squibb Company Antibodies against IL-7R alpha subunit and uses thereof
WO2020247623A1 (en) * 2019-06-05 2020-12-10 Regeneron Pharmaceuticals, Inc. Non-human animals having a limited lambda light chain repertoire expressed from the kappa locus and uses thereof
WO2021003152A1 (en) * 2019-07-01 2021-01-07 Trianni, Inc. Transgenic mammals and methods of use thereof
WO2021231732A1 (en) 2020-05-15 2021-11-18 Bristol-Myers Squibb Company Antibodies to garp
WO2024163477A1 (en) 2023-01-31 2024-08-08 University Of Rochester Immune checkpoint blockade therapy for treating staphylococcus aureus infections

Also Published As

Publication number Publication date
EP2905338B8 (en) 2018-01-24
US9066502B2 (en) 2015-06-30
KR102059909B1 (en) 2019-12-27
JP2013531501A (en) 2013-08-08
KR102320944B1 (en) 2021-11-04
SI3034608T1 (en) 2019-06-28
HUE029691T2 (en) 2017-03-28
CY1117537T1 (en) 2017-04-26
NZ707198A (en) 2016-04-29
NZ627119A (en) 2015-05-29
AU2011271043A8 (en) 2016-01-21
IL269078B (en) 2021-05-31
IL282872B (en) 2022-04-01
ZA201404601B (en) 2016-02-24
ZA201404600B (en) 2015-09-30
SG10201504568YA (en) 2015-07-30
US20130326647A1 (en) 2013-12-05
EP2480676B1 (en) 2016-04-06
EP2480675B1 (en) 2016-04-06
JP6243384B2 (en) 2017-12-06
CN103068994A (en) 2013-04-24
KR102211911B1 (en) 2021-02-05
SI2480676T1 (en) 2016-10-28
KR20130121814A (en) 2013-11-06
LT2568049T (en) 2016-10-10
HK1170766A1 (en) 2013-03-08
HRP20171666T1 (en) 2017-12-15
HRP20190807T1 (en) 2019-08-23
IL244450A0 (en) 2016-04-21
JP2023133554A (en) 2023-09-22
IL223720A (en) 2017-05-29
AU2011271043A9 (en) 2015-10-01
EP2480675A1 (en) 2012-08-01
JP6545773B2 (en) 2019-07-17
US9540452B2 (en) 2017-01-10
US20150176002A1 (en) 2015-06-25
ES2646052T3 (en) 2017-12-11
US9206261B2 (en) 2015-12-08
PL3034608T3 (en) 2019-08-30
RS58736B1 (en) 2019-06-28
RU2601297C2 (en) 2016-10-27
SI2480675T1 (en) 2016-08-31
US20150246976A1 (en) 2015-09-03
LT2905338T (en) 2017-12-27
RU2013102596A (en) 2014-07-27
SI2568049T1 (en) 2016-10-28
KR20190142436A (en) 2019-12-26
AU2011271046B2 (en) 2015-10-01
US20120070861A1 (en) 2012-03-22
CY1118126T1 (en) 2017-06-28
JP2018201528A (en) 2018-12-27
US20150173332A1 (en) 2015-06-25
US9035128B2 (en) 2015-05-19
IL259965A (en) 2018-07-31
ME03386B (en) 2020-01-20
MX347322B (en) 2017-04-21
SG186390A1 (en) 2013-01-30
KR20180135996A (en) 2018-12-21
IL300712B1 (en) 2024-07-01
SMT201600212B (en) 2016-08-31
RU2013102595A (en) 2014-07-27
HUE044001T2 (en) 2019-09-30
RS56589B1 (en) 2018-02-28
ME02442B (en) 2016-09-20
KR20230036157A (en) 2023-03-14
JP5988969B2 (en) 2016-09-07
JP6341972B2 (en) 2018-06-13
BR112012032991A8 (en) 2020-09-29
HK1226766A1 (en) 2017-10-06
MY195212A (en) 2023-01-11
PL2568049T3 (en) 2017-03-31
EP2568049A1 (en) 2013-03-13
JP2017012204A (en) 2017-01-19
CN104342455B (en) 2017-05-31
CA2804311A1 (en) 2011-12-29
KR101934852B1 (en) 2019-01-04
US9334333B2 (en) 2016-05-10
JP6963542B2 (en) 2021-11-10
BR112012032991A2 (en) 2015-10-06
SMT201600213B (en) 2016-08-31
RS55037B1 (en) 2016-12-30
SG186391A1 (en) 2013-01-30
JP6073441B2 (en) 2017-02-01
US20160057979A1 (en) 2016-03-03
BR112012032991B1 (en) 2021-08-10
KR102266097B1 (en) 2021-06-18
PT2905338T (en) 2017-11-10
HUE030285T2 (en) 2017-05-29
EP2480676A1 (en) 2012-08-01
JP2020128440A (en) 2020-08-27
US20240327785A1 (en) 2024-10-03
EP3456832A1 (en) 2019-03-20
KR20130027555A (en) 2013-03-15
IL291301B1 (en) 2023-03-01
PT2480676E (en) 2016-06-09
KR20220150430A (en) 2022-11-10
HK1183321A1 (en) 2013-12-20
US20160060359A1 (en) 2016-03-03
US9399683B2 (en) 2016-07-26
KR102193823B1 (en) 2020-12-22
CY1119478T1 (en) 2018-03-07
IL255179B (en) 2018-06-28
NZ707200A (en) 2016-04-29
MY194456A (en) 2022-11-30
KR20190014576A (en) 2019-02-12
RU2016119423A (en) 2018-11-07
RS54891B1 (en) 2016-10-31
HUE029692T2 (en) 2017-03-28
JP6009441B2 (en) 2016-10-19
MX348942B (en) 2017-07-04
US9029628B2 (en) 2015-05-12
IL247386A (en) 2017-07-31
HRP20160794T1 (en) 2016-08-12
JP7236409B2 (en) 2023-03-09
ME02902B (en) 2018-04-20
JP2017006152A (en) 2017-01-12
JP2016010417A (en) 2016-01-21
MY157477A (en) 2016-06-15
KR20190073584A (en) 2019-06-26
BR122020013427B1 (en) 2021-08-03
US9012717B2 (en) 2015-04-21
IL313063A (en) 2024-07-01
CN103068994B (en) 2016-01-20
US20190153384A1 (en) 2019-05-23
CA2804311C (en) 2017-09-12
ZA201506598B (en) 2017-03-29
MY195217A (en) 2023-01-11
US9163092B2 (en) 2015-10-20
US20170258059A1 (en) 2017-09-14
IL269078A (en) 2019-11-28
US20130323790A1 (en) 2013-12-05
MX336344B (en) 2016-01-15
RS55042B1 (en) 2016-12-30
JP2020062061A (en) 2020-04-23
SI2905338T1 (en) 2017-12-29
MX2022002117A (en) 2022-03-17
DK3034608T3 (en) 2019-05-06
US9226484B2 (en) 2016-01-05
ES2575223T3 (en) 2016-06-27
IL264634B (en) 2019-09-26
US20150089680A1 (en) 2015-03-26
KR102462042B1 (en) 2022-11-03
CY1122877T1 (en) 2021-05-05
JP2016010415A (en) 2016-01-21
JP2021061863A (en) 2021-04-22
US20150351371A1 (en) 2015-12-10
MX2012015300A (en) 2013-05-01
CN104404050B (en) 2018-06-08
RU2016119423A3 (en) 2019-11-19
EP3034608B1 (en) 2019-01-30
LT2480675T (en) 2016-10-10
JP2019033765A (en) 2019-03-07
CA2803864C (en) 2017-05-16
KR101970944B1 (en) 2019-04-23
DK2905338T3 (en) 2017-11-06
US20140137275A1 (en) 2014-05-15
EP2905338A1 (en) 2015-08-12
KR101975884B1 (en) 2019-05-10
LT3034608T (en) 2019-05-27
MX2012015298A (en) 2013-05-01
US9844212B2 (en) 2017-12-19
CN104342455A (en) 2015-02-11
HUE036597T2 (en) 2018-07-30
US9850462B2 (en) 2017-12-26
IL291301A (en) 2022-05-01
KR20200064166A (en) 2020-06-05
CN103068993B (en) 2016-01-06
US20150246977A1 (en) 2015-09-03
DK2480675T3 (en) 2016-08-01
EP2568049B1 (en) 2016-04-13
US20120073004A1 (en) 2012-03-22
IL282872A (en) 2021-06-30
CY1117692T1 (en) 2017-05-17
HRP20160497T1 (en) 2016-07-15
IL244450A (en) 2017-11-30
IL291301B2 (en) 2023-07-01
EP2905338B1 (en) 2017-08-02
US20200239837A1 (en) 2020-07-30
DK2480676T3 (en) 2016-06-20
CA2803864A1 (en) 2011-12-29
JP2018201527A (en) 2018-12-27
PL2480675T3 (en) 2017-03-31
PT2568049T (en) 2016-07-11
ME02440B (en) 2016-09-20
JP2018023403A (en) 2018-02-15
CN103068993A (en) 2013-04-24
JP2013532974A (en) 2013-08-22
JP2022066449A (en) 2022-04-28
IL259965B (en) 2019-02-28
KR20210134424A (en) 2021-11-09
ZA201300063B (en) 2014-09-25
IL223719A (en) 2016-10-31
EP3034608A1 (en) 2016-06-22
US10266803B2 (en) 2019-04-23
US20180064078A1 (en) 2018-03-08
KR20180135997A (en) 2018-12-21
ME02444B (en) 2016-09-20
US9206263B2 (en) 2015-12-08
PT3034608T (en) 2019-05-28
SMT201600229B (en) 2016-08-31
US9006511B2 (en) 2015-04-14
RU2590594C2 (en) 2016-07-10
NZ626979A (en) 2015-05-29
AU2011271046A1 (en) 2013-01-31
KR102506001B1 (en) 2023-03-07
US20190203171A1 (en) 2019-07-04
EP3205726A1 (en) 2017-08-16
KR101945352B1 (en) 2019-02-07
CN104404050A (en) 2015-03-11
PL2480676T3 (en) 2016-10-31
MY195214A (en) 2023-01-11
US9150662B2 (en) 2015-10-06
KR20190049932A (en) 2019-05-09
KR102001430B1 (en) 2019-07-18
US20170107484A1 (en) 2017-04-20
SG10201504324UA (en) 2015-07-30
US20150173331A1 (en) 2015-06-25
KR102118565B1 (en) 2020-06-03
NZ605751A (en) 2014-10-31
HRP20160865T1 (en) 2016-10-07
KR20190014578A (en) 2019-02-12
IL255179A0 (en) 2017-12-31
KR20210073609A (en) 2021-06-18
ES2576928T3 (en) 2016-07-12
NO2905338T3 (en) 2017-12-30
KR101991234B1 (en) 2019-06-20
NZ605758A (en) 2014-08-29
US20150320023A1 (en) 2015-11-12
WO2011163314A1 (en) 2011-12-29
ES2721749T3 (en) 2019-08-05
HK1168384A1 (en) 2012-12-28
ES2570131T3 (en) 2016-05-17
US9394373B2 (en) 2016-07-19
AU2011271043A1 (en) 2013-01-31
KR20200143511A (en) 2020-12-23
TR201905992T4 (en) 2019-05-21
MX347318B (en) 2017-04-21
US9206262B2 (en) 2015-12-08
IL300712A (en) 2023-04-01
DK2568049T3 (en) 2016-08-01
AU2011271043B2 (en) 2015-10-01
KR20210013376A (en) 2021-02-03
BR112012033248A2 (en) 2017-11-28
MY165287A (en) 2018-03-21
PT2480675T (en) 2016-07-11
PL2905338T3 (en) 2018-01-31
RU2724736C2 (en) 2020-06-25
ZA201300062B (en) 2014-09-25

Similar Documents

Publication Publication Date Title
US20200239837A1 (en) Human lambda light chain mice
AU2015275243B2 (en) Mice expressing a light chain with human lambda variable and mouse constant regions
AU2015275242B2 (en) Hybrid light chain mice
AU2011271043B8 (en) Mice expressing a light chain with human lambda variable and mouse constant regions

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 201180038415.2

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 11728508

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2011728508

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 223719

Country of ref document: IL

WWE Wipo information: entry into national phase

Ref document number: MX/A/2012/015300

Country of ref document: MX

ENP Entry into the national phase

Ref document number: 2013516714

Country of ref document: JP

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2804311

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 1201006719

Country of ref document: TH

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 20137001586

Country of ref document: KR

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2013102596

Country of ref document: RU

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2011271043

Country of ref document: AU

Date of ref document: 20110622

Kind code of ref document: A

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112012033248

Country of ref document: BR

WWE Wipo information: entry into national phase

Ref document number: 244450

Country of ref document: IL

WWE Wipo information: entry into national phase

Ref document number: P-2016/0483

Country of ref document: RS

REG Reference to national code

Ref country code: BR

Ref legal event code: B01E

Ref document number: 112012033248

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 112012033248

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20121226