Genetic engineering of non-human animals for the production of chimeric antibodies
The invention provides non-human cells and mammals having a genome encoding chimeric antibodies and methods of producing transgenic cells and mammals. Certain aspects of the invention include chimeric antibodies, humanized antibodies, pharmaceutical compositions and kits. Certain aspects of the invention also relate to diagnostic and treatment methods using the antibodies of the invention.
1. An in vitro method of producing a mammalian cell whose genome comprises a synthetic transgene that encodes a chimeric immunoglobulin heavy chain, wherein said immunoglobulin heavy chain comprises a chimeric constant region, said method comprising the steps of:
designing one or more DNA constructs in silico, wherein said one or more constructs comprise polynucleotide sequences comprising one or more human V, D and/or J gene segments and a chimeric constant region comprising a human CH1 gene segment, a human upper hinge region gene segment, a non-human CH2 gene segment, and a non-human CH3 segment;
producing said one or more DNA constructs; and
introducing the one or more constructs into the genome of a mammalian cell, wherein the genome of the mammalian cell comprises the synthetic transgene that encodes the chimeric immunoglobulin heavy chain comprising the chimeric constant region comprising a human CH1, a human upper hinge region, a non-human CH2, and a non-human CH3.
2. An isolated mammalian cell produced according to the method of claim 1 .
3. An isolated mammalian cell whose genome comprises a synthetic transgene encoding a chimeric antibody, or an antigen-binding fragment thereof, wherein the chimeric antibody or antigen-binding fragment thereof comprises a chimeric immunoglobulin heavy chain, wherein said chimeric immunoglobulin heavy chain comprises a human immunoglobulin heavy chain variable domain and a chimeric immunoglobulin heavy chain constant region comprising a human CH1 domain, a human upper hinge region, a non-human CH2 domain, and a non-human CH3 domain.
4. An in vitro method of producing a mammalian cell whose genome comprises a synthetic transgene, wherein upon expression of the synthetic transgene rearrangement occurs to produce a chimeric immunoglobulin heavy chain, wherein the chimeric immunoglobulin heavy chain comprises a variable domain and a chimeric immunoglobulin heavy chain constant region, said method comprising the steps of:
designing one or more DNA constructs in silico, wherein said one or more constructs comprise polynucleotide sequences comprising one or more human V, D and J gene segments and a chimeric constant region comprising a human CH1 gene segment, a human upper hinge region gene segment, a non-human CH2 gene segment, and a non-human CH3 segment;
producing said one or more DNA constructs; and
introducing the one or more constructs into the genome of a mammalian cell, wherein the genome of the mammalian cell comprises the synthetic transgene comprising one or more human V, D and J gene segments, a human CH1 gene segment, a human upper hinge region gene segment, a non-human CH2 gene segment, and a non-human CH3 segment, wherein upon expression of the synthetic transgene rearrangement occurs to produce a chimeric immunoglobulin heavy chain comprising a human immunoglobulin heavy chain variable domain and a chimeric immunoglobulin heavy chain constant region comprising a human CH1 domain, a human upper hinge region, a non-human CH2 domain and a non-human CH3 domain.
5. An isolated mammalian cell whose genome comprises a synthetic transgene comprising a human heavy chain V gene segment, a human heavy chain D gene segment, a human heavy chain J gene segment, a human CH1 gene segment, a human upper hinge region gene segment, a non-human CH2 gene segment, and a non-human CH3 gene segment, wherein upon expression of the synthetic transgene rearrangement occurs to produce a chimeric immunoglobulin heavy chain comprising a human heavy chain variable domain and a chimeric heavy chain constant region comprising a human CH1 domain, a human upper hinge region, a non-human CH2 domain, and a non-human CH3 domain.
6. The in vitro method according to claim 1 , further comprising the steps of:
designing a second DNA construct in silico, wherein said construct comprises a non-endogenous immunoglobulin light chain;
producing said second DNA construct; and
introducing the second construct into the genome of the cell.
7. The in vitro method according to claim 6 , wherein the non-endogenous light chain comprises one or more human Vκ gene segments.
8. The in vitro method according to claim 7 , wherein the non-endogenous light chain further comprises one or more human Jκ and Cκ gene segments.
9. The in vitro method according to claim 6 , wherein the non-endogenous light chain comprises one or more human Vλ, gene segments.
10. The in vitro method according to claim 9 , wherein the non-endogenous light chain further comprises one or more human Jλ-Cλ gene segment pairs.
11. The isolated mammalian cell according to claim 3 , wherein said genome further comprises a non-endogenous immunoglobulin light chain.
12. The cell according to claim 11 , wherein said genome comprises a non-endogenous Igκ light chain and a non-endogenous Igλ light chain.
13. The isolated mammalian cell according to claim 3 , wherein the cell comprises an inactivated endogenous immunoglobulin heavy chain locus.