胸腺上皮细胞。

IF 26.9 1区 医学 Q1 IMMUNOLOGY
Annual review of immunology Pub Date : 2017-04-26 Epub Date: 2017-02-10 DOI:10.1146/annurev-immunol-051116-052320
Jakub Abramson, Graham Anderson
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引用次数: 0

摘要

胸腺内 T 细胞的发育是一个复杂的过程,有赖于胸腺基质细胞微环境的持续引导。胸腺基质内的胸腺上皮由高度特化的细胞组成,具有高度的解剖学、表型和功能异质性。这些特性共同要求胸腺细胞的发育偏向于产生自我耐受和功能合格的 T 细胞。胸腺上皮细胞(TECs)的重要性体现在其功能障碍与多种疾病之间的明显联系上,而自身免疫和免疫缺陷是这些疾病的主要组成部分。因此,胸腺上皮细胞是细胞疗法恢复有效免疫系统功能的一个有吸引力的靶点。控制 TEC 发育的途径和分子调控因子以及它们对 T 细胞发育特定阶段的影响正变得越来越清晰。在此,我们回顾了控制 TEC 发育、功能、功能障碍和再生的细胞和分子机制的历史和最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thymic Epithelial Cells.

Intrathymic T cell development is a complex process that depends upon continuous guidance from thymus stromal cell microenvironments. The thymic epithelium within the thymic stroma comprises highly specialized cells with a high degree of anatomic, phenotypic, and functional heterogeneity. These properties are collectively required to bias thymocyte development toward production of self-tolerant and functionally competent T cells. The importance of thymic epithelial cells (TECs) is evidenced by clear links between their dysfunction and multiple diseases where autoimmunity and immunodeficiency are major components. Consequently, TECs are an attractive target for cell therapies to restore effective immune system function. The pathways and molecular regulators that control TEC development are becoming clearer, as are their influences on particular stages of T cell development. Here, we review both historical and the most recent advances in our understanding of the cellular and molecular mechanisms controlling TEC development, function, dysfunction, and regeneration.

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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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