Marrack P, Kappler J
Howard Hughes Medical Institute, Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.
Science. 1987 Nov 20;238(4830):1073-9. doi: 10.1126/science.3317824.
The primary structure of T cell receptor proteins and genes is well understood. Immunologists are now trying to understand the properties of these interesting molecules. Evidence suggests that T cell alpha beta receptors recognize a complex of an antigen-derived peptide bound to one of the cell-surface products of the major histocompatibility complex (MHC) genes. It is likely that alpha beta receptors and MHC proteins have coevolved to have some affinity for each other. During T cell development in the thymus, cells bearing self-reactive receptors are deleted by the mechanisms of tolerance, and cells are preferentially allowed to mature if they bear receptors that will be able to recognize antigen plus self-MHC after they have become full-fledged T cells. Some explanations for these phenomena have been tested, but no satisfactory theory can yet be proposed to account for them.
T细胞受体蛋白和基因的一级结构已为人熟知。免疫学家们目前正试图了解这些有趣分子的特性。有证据表明,T细胞αβ受体识别与主要组织相容性复合体(MHC)基因的一种细胞表面产物结合的抗原衍生肽复合物。αβ受体和MHC蛋白很可能已经共同进化,从而彼此具有一定亲和力。在胸腺中T细胞发育期间,带有自身反应性受体的细胞通过耐受机制被清除,而如果细胞带有在成为成熟T细胞后能够识别抗原加自身MHC的受体,则这些细胞会被优先允许成熟。对这些现象的一些解释已经得到验证,但尚未能提出令人满意的理论来解释它们。