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效应性 CD4 T 细胞群体的分化(*)。

Differentiation of effector CD4 T cell populations (*).

机构信息

Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892-1892, USA.

出版信息

Annu Rev Immunol. 2010;28:445-89. doi: 10.1146/annurev-immunol-030409-101212.


DOI:10.1146/annurev-immunol-030409-101212
PMID:20192806
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3502616/
Abstract

CD4 T cells play critical roles in mediating adaptive immunity to a variety of pathogens. They are also involved in autoimmunity, asthma, and allergic responses as well as in tumor immunity. During TCR activation in a particular cytokine milieu, naive CD4 T cells may differentiate into one of several lineages of T helper (Th) cells, including Th1, Th2, Th17, and iTreg, as defined by their pattern of cytokine production and function. In this review, we summarize the discovery, functions, and relationships among Th cells; the cytokine and signaling requirements for their development; the networks of transcription factors involved in their differentiation; the epigenetic regulation of their key cytokines and transcription factors; and human diseases involving defective CD4 T cell differentiation.

摘要

CD4 T 细胞在介导对各种病原体的适应性免疫中发挥关键作用。它们也参与自身免疫、哮喘和过敏反应以及肿瘤免疫。在特定细胞因子环境中 TCR 激活时,初始 CD4 T 细胞可分化为几种 T 辅助(Th)细胞谱系之一,包括 Th1、Th2、Th17 和 iTreg,其特征是细胞因子产生和功能模式。在这篇综述中,我们总结了 Th 细胞的发现、功能和关系;它们发育的细胞因子和信号要求;参与它们分化的转录因子网络;它们关键细胞因子和转录因子的表观遗传调控;以及涉及缺陷 CD4 T 细胞分化的人类疾病。

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[1]
Differentiation of effector CD4 T cell populations (*).

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[3]
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[4]
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[7]
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本文引用的文献

[1]
Pillars Article: Control of Regulatory T Cell Development by the Transcription Factor Foxp3. Science 2003. 299: 1057-1061.

J Immunol. 2017-2-1

[2]
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J Exp Med. 2009-11-23

[3]
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Nat Immunol. 2009-12

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Dec2 promotes Th2 cell differentiation by enhancing IL-2R signaling.

J Immunol. 2009-11-15

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Runx proteins regulate Foxp3 expression.

J Exp Med. 2009-10-26

[6]
CCCTC-binding factor and the transcription factor T-bet orchestrate T helper 1 cell-specific structure and function at the interferon-gamma locus.

Immunity. 2009-10-16

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Immunity. 2009-10-16

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Indispensable role of the Runx1-Cbfbeta transcription complex for in vivo-suppressive function of FoxP3+ regulatory T cells.

Immunity. 2009-10-16

[9]
CD4+ regulatory T cells control TH17 responses in a Stat3-dependent manner.

Science. 2009-10-1

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Runx-CBFbeta complexes control expression of the transcription factor Foxp3 in regulatory T cells.

Nat Immunol. 2009-11

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