Homologous recombination for universal donor cells and chimeric mammalian hosts
AssigneesCell Genesys, Inc., Univ. of North Carolina at Chapel Hill
InventorsRaju Kucherlapati, Beverly H. Koller, Oliver Smithies
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Abstract
Homologous recombination is employed to inactivate genes, particularly genes associated with MHC antigens. Particularly, the .beta..sub.2 -microglobulin gene is inactivated for reducing or eliminating Class I MHC antigens. The resulting cells may be used as universal donors. In addition, embryonic stem cells may be modified by homologous recombination for use in producing chimeric or transgenic mammalian hosts, which may be used as source of universal donor organs, or as models for drug and transplantation therapies.
Claims12
A method for producing a genetically engineered human epithelial cell lacking functional Class I major histocompatibility (MHC) antigens as a result of introduction of a lesion at each of the .beta..sub.2 -microglobulin loci by transformation of said human cell with at least one DNA construct comprising a sequence homologous with at least a portion of said locus and said lesion and integration of said construct at said loci, said method comprising:
- transforming a host cell with said DNA construct, wherein said construct comprises a marker gene for selection of host cells comprising said DNA;
- screening selected cells comprising said construct for homologous integration;
- transforming cells having homologous integration with said construct;
- and selecting cells lacking .beta..sub.2 -microglobulin on the surface by the absence of .beta..sub.2 -microglobulin.
A genetically engineered human epithelial cell lacking functional Class I major histocompatibility complex (MHC) antigens as a result of introduction of a lesion at each of the .beta..sub.2 -microglobulin loci by transformation of said human cell with at least one DNA construct comprising a sequence homologous with at least a portion of said loci and said lesion and integration of said construct at said loci.
A method for producing a genetically engineered murine epithelial cell lacking functional Class I major histocompatibility (MHC) antigens as a result of introduction of a lesion at each of the .beta..sub.2 -microglobulin loci of a subunit of said antigen by transformation of said mammalian cell with at least one DNA construct comprising a sequence homologous with at least a portion of said locus and said lesion and integration of said construct at said loci, said method comprising:
- transforming a host cell with said DNA construct, wherein said construct comprises a marker gene for selection of host cells comprising said DNA;
- screening selected cells comprising said construct for homologous integration;
- transforming cells having homologous integration with said construct;
- and selecting cells lacking .beta..sub.2 -microglobulin on the surface by the absence of .beta..sub.2 -microglobulin.
A genetically engineered murine epithelial cell lacking functional Class I major histocompatibility complex (MHC) antigens as a result of introduction of a lesion at each of the .beta..sub.2 -microglobulin loci by transformation of said murine cell with at least one DNA construct comprising a sequence homologous with at least a portion of said loci and said lesion and integration of said construct at said loci.
Dependencies are inferred from the claim text.