Chambers C A, Allison J P
Department of Molecular and Cellular Biology, Cancer Research Laboratory, University of California, Berkeley, CA 94720, USA.
Curr Opin Immunol. 1997 Jun;9(3):396-404. doi: 10.1016/s0952-7915(97)80087-8.
Antigen-specific T cell responses have primarily been considered in terms of activation signals delivered through the TCR and the co-stimulatory molecule CD28. In the past few years, studies have demonstrated the critical importance of inhibitory signals for regulating lymphocyte activation. CD28 and its homologue cytotoxic T lymphocyte antigen-4 (CTLA-4) share the same counter-receptors on antigen-presenting cells, but recent experiments have shown that CD28 and CTLA-4 have opposite effects on T cell activation. The mechanisms responsible for integrating these activation and inhibitory signals at the cellular and molecular levels are just beginning to be elucidated.
抗原特异性T细胞反应主要是根据通过T细胞受体(TCR)和共刺激分子CD28传递的激活信号来考虑的。在过去几年中,研究已经证明抑制性信号对于调节淋巴细胞激活至关重要。CD28及其同源物细胞毒性T淋巴细胞抗原4(CTLA-4)在抗原呈递细胞上共享相同的反受体,但最近的实验表明,CD28和CTLA-4对T细胞激活具有相反的作用。在细胞和分子水平上整合这些激活和抑制信号的机制刚刚开始被阐明。