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Type 1 regulatory T cells: a new mechanism of peripheral immune tolerance

机译:1型调节性T细胞:外周免疫耐受的新机制

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摘要

The lack of immune response to an antigen, a process known as immune tolerance, is essential for the preservation of immune homeostasis. To date, two mechanisms that drive immune tolerance have been described extensively: central tolerance and peripheral tolerance. Under the new nomenclature, thymus-derived regulatory T (tTreg) cells are the major mediators of central immune tolerance, whereas peripherally derived regulatory T (pTreg) cells function to regulate peripheral immune tolerance. A third type of Treg cells, termed iTreg, represents only the in vitro-induced Treg cells. Depending on whether the cells stably express Foxp3, pTreg, and iTreg cells may be divided into two subsets: the classical CD4+Foxp3+ Treg cells and the CD4+Foxp3 type 1 regulatory T (Tr1) cells. This review focuses on the discovery, associated biomarkers, regulatory functions, methods of induction, association with disease, and clinical trials of Tr1 cells.
机译:缺乏对抗原的免疫反应(一种称为免疫耐受的过程),对于保持免疫稳态是至关重要的。迄今为止,已经广泛描述了驱动免疫耐受的两种机制:中枢耐受和外周耐受。根据新的命名法,胸腺来源的调节性T(tTreg)细胞是中枢免疫耐受的主要介质,而外周来源的调节性T(pTreg)细胞则起着调节外周免疫耐受的作用。第三种类型的Treg细胞称为iTreg,仅代表体外诱导的Treg细胞 。根据细胞是否稳定表达Foxp3,pTreg和iTreg细胞,可以将其分为两个子集:经典CD4 + Foxp3 + Treg细胞和CD4 + Foxp3 - 1型调节性T(Tr1)细胞 。这篇综述着重于Tr1细胞的发现,相关的生物标记,调节功能,诱导方法,与疾病的关联以及临床试验。

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