Rabinowitz J D, Tate K, Lee C, Beeson C, McConnell H M
Department of Chemistry, Stanford University, Stanford, CA 94305, USA.
Proc Natl Acad Sci U S A. 1997 Aug 5;94(16):8702-7. doi: 10.1073/pnas.94.16.8702.
Helper T cells are triggered by molecular complexes of antigenic peptides and class II proteins of the major histocompatibility complex. The formation of stable complexes between class II major histocompatibility complex proteins and antigenic peptides is often accompanied by the formation of a short-lived complex. In this report, we describe T cell recognition of two distinct complexes, one short-lived and the other long-lived, formed during the binding of an altered myelin basic protein peptide to I-Ak. One myelin basic protein-specific T cell clone is triggered by only the short-lived complex, and another is triggered by only the stable complex. Thus, a single peptide bound to a particular class II molecule can activate different T cells depending on the conditions of the binding reaction.
辅助性T细胞由主要组织相容性复合体的抗原肽与II类蛋白的分子复合物触发。II类主要组织相容性复合体蛋白与抗原肽之间稳定复合物的形成通常伴随着短暂复合物的形成。在本报告中,我们描述了T细胞对两种不同复合物的识别,一种是短暂存在的,另一种是长期存在的,它们在改变的髓鞘碱性蛋白肽与I-Ak结合过程中形成。一个髓鞘碱性蛋白特异性T细胞克隆仅由短暂复合物触发,另一个则仅由稳定复合物触发。因此,与特定II类分子结合的单个肽可以根据结合反应的条件激活不同的T细胞。