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Article
Nature Genetics  15, 146 - 156 (1997)
doi:10.1038/ng0297-146

Functional transplant of megabase human immunoglobulin loci recapitulates human antibody response in mice

Michael J. Mendez2, Larry L. Green1, Jose R.F. Corvalan1, Xiao-Chi Jia1, Catherine E. Maynard-Currie1, Xiao-dong Yang1, Michael L. Gallo1, Donna M. Louie1, Doris V. Lee1, Karen L. Erickson1, Jac Luna2, Catherine M.-N. Roy1, Hadi Abderrahim2, Ford Kirschenbaum2, Masato Noguchi2, Douglas H. Smith2, Atsushi Fukushima2, Joanna F. Hales1, Mitchell H. Finer2, C. Geoffrey Davis1, Krisztina M. Zsebo2 & Aya Jakobovits1

  1Abgenix, Inc., 7601 Dumbarton Circle, Fremont, California 94555, USA.

  2Cell Genesys, Inc., Foster City, California 94404, USA. Current address of M.N and A.F.: JT Pharmaceutical Basic Research Laboratories, Yokohama, Japan.

We constructed two megabase-sized YACs containing large contiguous fragments of the human heavy and kappa (kappa) light chain immunoglobulin (Ig) loci in nearly germline configuration, including approximately 66 VH and 32 Vkappa genes. We introduced these YACs into Ig-inactivated mice and observed human antibody production which closely resembled that seen in humans in all respects, including gene rearrangement, assembly, and repertoire. Diverse Ig gene usage together with somatic hypermutation enables the mice to generate high affinity fully human antibodies to multiple antigens, including human proteins. Our results underscore the importance of the large Ig fragments with multiple V genes for restoration of a normal humoral immune response. These mice are likely to be a valuable tool for the generation of therapeutic antibodies.

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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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