Sultan P, Schechner J S, McNiff J M, Hochman P S, Hughes C C, Lorber M I, Askenase P W, Pober J S
Molecular Cardiobiology Program, Yale University School of Medicine, New Haven, CT 06536, USA.
Nat Biotechnol. 1997 Aug;15(8):759-62. doi: 10.1038/nbt0897-759.
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.
在免疫缺陷小鼠中建立了人皮肤同种异体移植损伤模型,该模型移植了来自不同供体的人外周血单核细胞,用于测试阻断人T细胞CD2与其主要配体LFA-3(CD58)相互作用的试剂是否能在体内抑制免疫反应。在这个模型中,人皮肤移植呈现出可重复的模式,即渐进性人T细胞浸润和人移植微血管损伤,类似于人初次皮肤移植排斥反应。针对人LFA-3的鼠单克隆抗体或人LFA-3-IgG1融合蛋白,而非同型对照抗体,均显著保护皮肤移植免受白细胞浸润和损伤。这些数据首次证明LFA-3在体内发挥作用,并确立了这种新模型测试人特异性免疫调节剂的能力。