Krieger N R, Yin D P, Fathman C G
Department of Medicine, Stanford University School of Medicine, California 94305, USA.
J Exp Med. 1996 Nov 1;184(5):2013-8. doi: 10.1084/jem.184.5.2013.
The generation of knockout mice with targeted gene disruption has provided a valuable tool for studying the immune response. Here we describe the use of CD4 and CD8 knockout mice to examine the role of CD4+ and CD8+ cells in initiating allotransplantation rejection. Pretreatment with a brief course of depletive anti-CD4 monoclonal antibody therapy allowed permanent survival of heart, but not skin, allografts transplanted across a major histocompatibility barrier. However, skin as well as heart grafts were permanently accepted in the CD4 knockout mice. Transfer of CD4+ cells into CD4 knockout recipient mice 1 d before skin engraftment reconstituted rejection, demonstrating that CD4+ cells are necessary for initiating rejection of allogeneic transplants. Major histocompatibility complex disparate heart and skin allografts transplanted into CD8 knockout recipients were rejected within 10 d. This study demonstrates that CD4+ but not CD8+ T cells are absolutely required to initiate allograft rejection.
通过靶向基因破坏产生基因敲除小鼠为研究免疫反应提供了一种有价值的工具。在此,我们描述了使用CD4和CD8基因敲除小鼠来研究CD4+和CD8+细胞在引发同种异体移植排斥反应中的作用。用一个短暂疗程的耗竭性抗CD4单克隆抗体疗法进行预处理,可使跨越主要组织相容性屏障移植的心脏同种异体移植物长期存活,但皮肤同种异体移植物则不能。然而,在CD4基因敲除小鼠中,皮肤和心脏移植物均被长期接受。在皮肤移植前1天,将CD4+细胞转移到CD4基因敲除受体小鼠中可重建排斥反应,表明CD4+细胞是引发同种异体移植排斥反应所必需的。移植到CD8基因敲除受体中的主要组织相容性复合体不相容的心脏和皮肤同种异体移植物在10天内被排斥。这项研究表明,引发同种异体移植排斥反应绝对需要CD4+而不是CD8+ T细胞。