Blockade of CD2-LFA-3 interactions protects human skin allografts in immunodeficient mouse/human chimeras

被引:55
作者
Sultan, P
Schechner, JS
McNiff, JM
Hochman, PS
Hughes, CCW
Lorber, MI
Askenase, PW
Pober, JS
机构
[1] YALE UNIV, SCH MED, MOL CARDIOBIOL PROGRAM, NEW HAVEN, CT 06536 USA
[2] YALE UNIV, SCH MED, DEPT BIOL, NEW HAVEN, CT 06536 USA
[3] YALE UNIV, SCH MED, DEPT DERMATOL, NEW HAVEN, CT 06536 USA
[4] YALE UNIV, SCH MED, DEPT PATHOL, NEW HAVEN, CT 06536 USA
[5] YALE UNIV, SCH MED, DEPT MED, NEW HAVEN, CT 06536 USA
[6] YALE UNIV, SCH MED, DEPT SURG, NEW HAVEN, CT 06536 USA
[7] BIOGEN INC, CAMBRIDGE, MA 02142 USA
[8] UNIV CALIF IRVINE, DEPT MOL BIOL & BIOCHEM, IRVINE, CA 92697 USA
关键词
animal model; transplantation; T lymphocytes; costimulatory molecules;
D O I
10.1038/nbt0897-759
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A human skin allograft injury model in immunodeficient mice, engrafted with human peripheral blood mononuclear cells from a different donor, has been used to test whether reagents that block human T cell CD2 interactions with its principal ligand, LFA-3 (CD58), can inhibit immune reactions in vivo. In this model, human skin grafts show a reproducible pattern of progressive human T-cell infiltration and human graft microvascular injury that resembles human first-set skin graft rejection. Murine Mab to human LFA-3 or human LFA-3-IgG1 fusion protein, but not isotype-matched control antibodies, each markedly protected skin grafts from leukocyte infiltration and injury. These data provide the first evidence that LFA-3 functions in vivo and establish the ability of this new model to test human-specific immune modulators.
引用
收藏
页码:759 / 762
页数:4
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