Harding F A, Allison J P
Department of Molecular and Cell Biology, University of California, Berkeley 94720.
J Exp Med. 1993 Jun 1;177(6):1791-6. doi: 10.1084/jem.177.6.1791.
The activation requirements for the generation of CD8+ cytotoxic T cells (CTL) are poorly understood. Here we demonstrate that in the absence of exogenous help, a CD28-B7 interaction is necessary and sufficient for generation of class I major histocompatibility complex-specific CTL. Costimulation is required only during the inductive phase of the response, and not during the effector phase. Transfection of the CD28 counter receptor, B7, into nonstimulatory P815 cells confers the ability to elicit P815-specific CTL, and this response can be inhibited by anti-CD28 Fab or by the chimeric B7-binding protein CTLA4Ig. Anti-CD28 monoclonal antibody (mAb) can provide a costimulatory signal to CD8+ T cells when the costimulatory capacity of splenic stimulators is destroyed by chemical fixation. CD28-mediated signaling provokes the release of interleukin 2 (IL-2) from the CD8+ CTL precursors, as anti-CD28 mAb could be substituted for by the addition of IL-2, and an anti-IL-2 mAb can block the generation of anti-CD28-induced CTL. CD4+ cells are not involved in the costimulatory response in the systems examined. We conclude that CD8+ T cell activation requires two signals: an antigen-specific signal mediated by the T cell receptor, and an additional antigen nonspecific signal provided via a CD28-B7 interaction.
对于生成CD8 + 细胞毒性T细胞(CTL)的激活要求,目前了解甚少。在此我们证明,在缺乏外源性辅助的情况下,CD28 - B7相互作用对于生成I类主要组织相容性复合体特异性CTL是必要且充分的。共刺激仅在反应的诱导阶段需要,而在效应阶段则不需要。将CD28的反受体B7转染到无刺激作用的P815细胞中,赋予了其引发P815特异性CTL的能力,并且这种反应可被抗CD28 Fab或嵌合性B7结合蛋白CTLA4Ig抑制。当脾刺激细胞的共刺激能力被化学固定破坏时,抗CD28单克隆抗体(mAb)可为CD8 + T细胞提供共刺激信号。CD28介导的信号传导促使CD8 + CTL前体细胞释放白细胞介素2(IL - 2),因为添加IL - 2可替代抗CD28 mAb,并且抗IL - 2 mAb可阻断抗CD28诱导的CTL的生成。在所研究的系统中,CD4 + 细胞不参与共刺激反应。我们得出结论,CD8 + T细胞激活需要两个信号:一个由T细胞受体介导的抗原特异性信号,以及一个通过CD28 - B7相互作用提供的额外的抗原非特异性信号。