Division of Molecular Immunology, German Cancer Research Center DKFZ, Heidelberg, Germany.
Curr Opin Immunol. 2010 Oct;22(5):601-8. doi: 10.1016/j.coi.2010.08.007. Epub 2010 Sep 27.
Naive T cells spend most of their time scanning the surface of dendritic cells (DCs), indicating that self-MHC/T cell receptor (TCR) interactions between these immune cells occur routinely in peripheral organs during the steady state. Peripheral self-MHC recognition on DCs drives seemingly opposing effects in the absence of inflammatory stimuli such as deletion of certain self-reactive T cells as well as maintenance of the T cell responsiveness to antigen, both of which shape the T cell repertoire and regulate T cell responses. Here we review recent data on the role of self-MHC recognition on steady-state DCs in the periphery and propose that interactions between T cells and steady-state DCs display an analogy with selection processes that occur in the thymus: high affinity TCR/self-MHC interactions in the periphery result in T cell deletion, while low/intermediate affinity interactions result in tonic TCR signalling that is required to keep T cells responsive to antigen.
幼稚 T 细胞大部分时间都在扫描树突状细胞 (DC) 的表面,这表明在稳态下,这些免疫细胞在周围器官中经常发生自身 MHC/T 细胞受体 (TCR) 相互作用。在没有炎症刺激的情况下,外周自身 MHC 对 DC 的识别会产生看似相反的影响,例如某些自身反应性 T 细胞的删除以及对抗原的 T 细胞反应性的维持,这两者都塑造了 T 细胞库并调节 T 细胞反应。在这里,我们回顾了关于外周稳态 DC 上的自身 MHC 识别在稳态中的作用的最新数据,并提出 T 细胞与稳态 DC 之间的相互作用与发生在胸腺中的选择过程具有类似性:外周高亲和力 TCR/自身 MHC 相互作用导致 T 细胞删除,而低/中等亲和力相互作用导致需要保持 T 细胞对抗原的反应性的紧张 TCR 信号。