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转化生长因子-β:它的耐受性如何?

TGF-beta: how tolerant can it be?

作者信息

Wahl Sharon M, Chen Wanjun

机构信息

Cellular Immunology Section, Oral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892-4352, USA.

出版信息

Immunol Res. 2003;28(3):167-79. doi: 10.1385/IR:28:3:167.

DOI:10.1385/IR:28:3:167
PMID:14713712
Abstract

A balance between an adequate immune response to an antigen or pathogen and tolerance is a prerequisite for normal immune homeostasis and the well-being of the host. In this complex self-regulation, multiple mechanisms have been implicated as contributing to the immune tolerance network, including apoptosis, anergy, and active suppression. Current excitement focuses on active suppression and new regulatory T cell-mediated pathways of immunosuppression that are being unraveled. Central to several of these pathways is transforming growth factor-beta (TGF-beta), a potent immunoregulatory cytokine that contributes to the function and generation of regulatory T cells.

摘要

对抗原或病原体产生充分的免疫反应与免疫耐受之间的平衡,是正常免疫稳态及宿主健康的先决条件。在这种复杂的自我调节过程中,多种机制被认为对免疫耐受网络有贡献,包括细胞凋亡、无反应性和主动抑制。当前的研究热点集中在主动抑制以及正在被揭示的由新型调节性T细胞介导的免疫抑制途径。这些途径中的几个关键因素是转化生长因子-β(TGF-β),它是一种强大的免疫调节细胞因子,对调节性T细胞的功能和生成有重要作用。

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本文引用的文献

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Conversion of peripheral CD4+CD25- naive T cells to CD4+CD25+ regulatory T cells by TGF-beta induction of transcription factor Foxp3.通过转化生长因子β诱导转录因子Foxp3,使外周CD4+CD25-初始T细胞转化为CD4+CD25+调节性T细胞。
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