T细胞受体
主要组织相容性复合体
退化(生物学)
MHC限制
生物
CD8型
T细胞
细胞生物学
计算生物学
抗原
遗传学
免疫学
免疫系统
作者
Catherine Mazza,Bernard Malissen
标识
DOI:10.1016/j.smim.2007.03.003
摘要
MHC-encoded molecules govern adaptive immune responses by presenting peptides to T cell receptors (TCRs). Based on TCR-MHC crystal structures, we revisit the extent of TCR binding degeneracy, a property with important biological consequences because the diversity of TCR ligands that can be encountered exceeds the number of T cell clones present in a person at any one time. We also discuss whether the approximate diagonal binding of TCR on MHC molecules is due to an intrinsic property of the TCR variable regions, or results from the action of the CD4 and CD8 coreceptors during intrathymic T cell selection. Finally, we discuss how MHC restriction of antigen recognition might have emerged during evolution.
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