Townsend A, Bodmer H
Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, United Kingdom.
Annu Rev Immunol. 1989;7:601-24. doi: 10.1146/annurev.iy.07.040189.003125.
The work discussed here offers a unified view of T-cell recognition and suggests that class-I and class-II molecules have a closely related function in the presentation of peptides to T lymphocytes. The epitopes recognized by class I-restricted T cells that have been defined with peptides in the 4-6 hr lysis assay have all been derived from endogenously synthesized proteins expressed by virus infected or transfected cells. Evidence is accumulating that a cytoplasmic degradation system may be involved in the generation of these epitopes. The analysis of the specificity of CTL responses with synthetic peptides has demonstrated the control of immune responses to isolated epitopes by class-I genes and the great diversity of the receptor repertoire for individual class-I-restricted epitopes.
这里所讨论的研究工作提供了关于T细胞识别的统一观点,并表明I类和II类分子在向T淋巴细胞呈递肽段的过程中具有密切相关的功能。在4 - 6小时裂解试验中用肽段确定的I类限制性T细胞识别的表位均来自病毒感染或转染细胞表达的内源性合成蛋白质。越来越多的证据表明,细胞质降解系统可能参与这些表位的产生。用合成肽对CTL反应特异性的分析已经证明了I类基因对分离表位免疫反应的控制以及单个I类限制性表位受体库的巨大多样性。