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调节辅助性T细胞分化的转录因子。

Transcription factors that regulate helper T cell differentiation.

作者信息

Usui Takashi

机构信息

Department of Rheumatology and Clinical Immunology, Kyoto University, Graduate School of Medicine, Kyoto, Japan.

出版信息

Nihon Rinsho Meneki Gakkai Kaishi. 2007 Dec;30(6):419-27. doi: 10.2177/jsci.30.419.

DOI:10.2177/jsci.30.419
PMID:18174670
Abstract

Antigen-specific CD4(+) helper T cell (Th cell) is a major player for acquired-immunity. Th cell distribute in the peripheral tissues after educations and selections in the thymus. By stimulation from antigen presenting cell (APC), Th cell differentiate into at least three types of effector Th cells by the cytokine environments and the kinds of co-stimulatory molecules on APC. One is Th1 cell which produces IFN-gamma mainly, and another is Th2 cell which produces IL-4, 5 and 13 mainly, and finally recently defined Th17 cell which produces IL-17 mainly, and these cells are charged with the a role for "cellular", "hormoral" and "inflammatory" immunity respectively. IL-12, STAT4 and T-bet signals are important for Th1 differentiation, and IL-4, STAT6 andGATA3 signals are important for Th2 differentiation, and IL-1beta, TGF-beta, IL-6, IL-23, STAT3, RORgammat signals are important for Th17 differentiation. This newly defined Th17 cell clearly makes a big progress for understanding the pathophysiology of many inflammatory conditions. In the near future, many biologics or compounds that regulate the production or function of IL-17 will be produced aggressively.

摘要

抗原特异性CD4(+)辅助性T细胞(Th细胞)是获得性免疫的主要参与者。Th细胞在胸腺中经过培育和选择后分布于外周组织。在抗原呈递细胞(APC)的刺激下,Th细胞根据细胞因子环境和APC上共刺激分子的种类分化为至少三种效应Th细胞。一种是主要产生干扰素-γ的Th1细胞,另一种是主要产生白细胞介素-4、5和13的Th2细胞,最后是最近定义的主要产生白细胞介素-17的Th17细胞,这些细胞分别在“细胞”、“体液”和“炎症”免疫中发挥作用。白细胞介素-12、信号转导和转录激活因子4(STAT4)以及T盒转录因子(T-bet)信号对Th1分化很重要,白细胞介素-4、STAT6以及GATA结合蛋白3(GATA3)信号对Th2分化很重要,白细胞介素-1β、转化生长因子-β(TGF-β)、白细胞介素-6、白细胞介素-23、STAT3、维甲酸相关孤儿受体γt(RORγt)信号对Th17分化很重要。这种新定义的Th17细胞在理解许多炎症性疾病的病理生理学方面显然取得了重大进展。在不久的将来,将会大力研发许多调节白细胞介素-17产生或功能的生物制剂或化合物。

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Transcription factors that regulate helper T cell differentiation.调节辅助性T细胞分化的转录因子。
Nihon Rinsho Meneki Gakkai Kaishi. 2007 Dec;30(6):419-27. doi: 10.2177/jsci.30.419.
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Role of antigen-presenting cells in the polarized development of helper T cell subsets: evidence for differential cytokine production by Th0 cells in response to antigen presentation by B cells and macrophages.抗原呈递细胞在辅助性T细胞亚群极化发育中的作用:Th0细胞对B细胞和巨噬细胞抗原呈递反应产生不同细胞因子的证据。
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Comprehensive intestinal T helper cell profiling reveals specific accumulation of IFN-γ+IL-17+coproducing CD4+ T cells in active inflammatory bowel disease.全面的肠道辅助性T细胞分析揭示了在活动性炎症性肠病中产生IFN-γ+IL-17+的CD4+ T细胞的特异性聚集。
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The key regulators of adult T helper cell responses, STAT6 and T-bet, are established in early life in mice.成年辅助性T细胞反应的关键调节因子STAT6和T-bet在小鼠生命早期就已确立。
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Cytotoxic T-lymphocyte antigen-4 inhibits GATA-3 but not T-bet mRNA expression during T helper cell differentiation.细胞毒性T淋巴细胞抗原4在辅助性T细胞分化过程中抑制GATA-3而非T-bet信使核糖核酸的表达。
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Suppressors of cytokine signaling proteins are differentially expressed in Th1 and Th2 cells: implications for Th cell lineage commitment and maintenance.细胞因子信号传导蛋白的抑制因子在Th1和Th2细胞中差异表达:对Th细胞谱系定向和维持的影响。
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Th17 cells: a new fate for differentiating helper T cells.辅助性T细胞分化的新命运:Th17细胞
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