胸腺T细胞选择的指导性提示。

IF 26.9 1区 医学 Q1 IMMUNOLOGY Annual review of immunology Pub Date : 2022-04-26 DOI:10.1146/annurev-immunol-101320-022432
Magali Irla
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引用次数: 17

摘要

胸腺中的T细胞发育过程中产生了高度多样的αβT细胞受体(TCRs),几乎能够识别任何病原体,也能识别自身抗原。然而,严格的开发计划支持选择能够对外来抗原做出反应的自我耐受的T细胞库。T细胞选择的步骤由皮质和髓质基质小生境控制,基质小生境主要由胸腺上皮细胞和树突状细胞组成。由这些专门的小生境提供的重要线索的整合,包括(a)由识别自身肽MHC复合物诱导的TCR信号强度,(b)共刺激信号,和(c)细胞因子信号,关键地控制T细胞库的选择。这篇综述讨论了我们目前对协调Foxp3+调节性T细胞的阳性选择、阴性选择和激动剂选择的信号的理解。它还强调了最近的进展,这些进展揭示了与T细胞选择有关的胸腺抗原呈递细胞亚群的功能多样性。
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Instructive Cues of Thymic T Cell Selection.
A high diversity of αβ T cell receptors (TCRs), capable of recognizing virtually any pathogen but also self-antigens, is generated during T cell development in the thymus. Nevertheless, a strict developmental program supports the selection of a self-tolerant T cell repertoire capable of responding to foreign antigens. The steps of T cell selection are controlled by cortical and medullary stromal niches, mainly composed of thymic epithelial cells and dendritic cells. The integration of important cues provided by these specialized niches, including (a) the TCR signal strength induced by the recognition of self-peptide-MHC complexes, (b) costimulatory signals, and (c) cytokine signals, critically controls T cell repertoire selection. This review discusses our current understanding of the signals that coordinate positive selection, negative selection, and agonist selection of Foxp3+ regulatory T cells. It also highlights recent advances that have unraveled the functional diversity of thymic antigen-presenting cell subsets implicated in T cell selection.
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来源期刊
Annual review of immunology
Annual review of immunology 医学-免疫学
CiteScore
57.20
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Immunology, in publication since 1983, focuses on basic immune mechanisms and molecular basis of immune diseases in humans. Topics include innate and adaptive immunity; immune cell development and differentiation; immune control of pathogens (viruses, bacteria, parasites) and cancer; and human immunodeficiency and autoimmune diseases. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license.
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