Kim Hee-Ok, Cho Jae-Ho
Academy of Immunology and Microbiology, Institute for Basic Science, Pohang 37673, Korea.
Division of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology, Pohang 37673, Korea.
Immune Netw. 2017 Aug;17(4):201-213. doi: 10.4110/in.2017.17.4.201. Epub 2017 Aug 23.
Post-thymic naïve T cells constitute a key cellular arm of adaptive immunity, with a well-known characteristic of the specificity and robustness of responses to cognate foreign antigens which is presented as a form of antigen-derived peptides bound to major histocompatibility complex (MHC) molecules by antigen-presenting cells (APCs). In a steady state, however, these cells are resting, quiescent in their activity, but must keep full ranges of functional integrity to mount rapid and robust immunity to cope with various infectious pathogens at any time and space. Such unique property of resting naïve T cells is not acquired in a default manner but rather requires an active mechanism. Although our understanding of exactly how this process occurs and what factors are involved remains incomplete, a particular role of self-recognition by T cells has grown greatly in recent years. In this brief review, we discuss recent data on how the interaction of T cells with self-peptide MHC ligands regulates their functional responsiveness and propose that variable strength of self-reactivity imposes distinctly different levels of functional competence and heterogeneity.
胸腺后初始T细胞构成了适应性免疫的关键细胞分支,具有众所周知的特性,即对同源外来抗原的反应具有特异性和稳健性,这种反应以抗原呈递细胞(APC)将抗原衍生肽与主要组织相容性复合体(MHC)分子结合的形式呈现。然而,在稳态下,这些细胞处于静止状态,活动不活跃,但必须保持全面的功能完整性,以便在任何时间和空间对各种感染性病原体迅速产生强大的免疫反应。静止初始T细胞的这种独特特性并非以默认方式获得,而是需要一种主动机制。尽管我们对这一过程究竟如何发生以及涉及哪些因素的理解仍不完整,但近年来T细胞自我识别的特殊作用已得到极大关注。在这篇简短的综述中,我们讨论了关于T细胞与自身肽MHC配体的相互作用如何调节其功能反应性的最新数据,并提出自我反应性的可变强度会导致不同水平的功能能力和异质性。