Regulation of T helper cell differentiation by interferon regulatory factor family members

被引:2
|
作者
Ruihua Zhang
Kang Chen
Liang Peng
Huabao Xiong
机构
[1] Mount Sinai School of Medicine,Department of Medicine
[2] Immunology Institute,Department of Gastroenterology
[3] Nanfang Hospital,undefined
[4] Southern Medical University,undefined
来源
Immunologic Research | 2012年 / 54卷
关键词
Interferon regulatory factor; T cell differentiation; IL-12; IFN-γ; IL-4; IL-17;
D O I
暂无
中图分类号
学科分类号
摘要
Interferon regulatory factors (IRFs) consist of a family of transcription factors with diverse functions in the transcriptional regulation of cellular responses in health and diseases. IRFs commonly contain a DNA-binding domain in the N-terminus, with most members also containing a C-terminal IRF-associated domain that mediates protein–protein interactions. Ten IRFs and several virus-encoded IRF homologs have been identified in mammals so far. In response to endogenous and microbial stimuli during an immune response, IRFs are activated, and selectively and cooperatively modulate the expression of key cytokine and transcription factors involved in T helper cell differentiation in T cells and/or antigen-presenting cells. This review focuses on recent advances in the understanding of IRF-mediated transcriptional regulation in T helper cell differentiation and discusses the implications on the development of cellular and humoral immune responses and the pathogenesis of immune disorders.
引用
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页码:169 / 176
页数:7
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