Mazza Catherine, Malissen Bernard
Centre d'Immunologie de Marseille-Luminy, Université de la Méditerranée, Case 906, 13288 Marseille Cedex 9, France.
Semin Immunol. 2007 Aug;19(4):225-35. doi: 10.1016/j.smim.2007.03.003. Epub 2007 May 22.
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.
主要组织相容性复合体(MHC)编码的分子通过将肽段呈递给T细胞受体(TCR)来调控适应性免疫反应。基于TCR-MHC晶体结构,我们重新审视了TCR结合简并性的程度,这一特性具有重要的生物学意义,因为可能遇到的TCR配体的多样性超过了任何时候一个人体内存在的T细胞克隆的数量。我们还讨论了TCR在MHC分子上近似对角线结合是由于TCR可变区的内在特性,还是胸腺内T细胞选择过程中CD4和CD8共受体作用的结果。最后,我们讨论了抗原识别的MHC限制性在进化过程中可能是如何出现的。