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Ringing the interferon alarm:: differential regulation of gene expression at the interface between innate and adaptive immunity
被引:116
作者:

Levy, DE
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机构:
NYU, Sch Med, Mol Oncol & Immunol Program, Dept Pathol, New York, NY 10016 USA NYU, Sch Med, Mol Oncol & Immunol Program, Dept Pathol, New York, NY 10016 USA

Marié, I
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机构: NYU, Sch Med, Mol Oncol & Immunol Program, Dept Pathol, New York, NY 10016 USA

Prakash, A
论文数: 0 引用数: 0
h-index: 0
机构: NYU, Sch Med, Mol Oncol & Immunol Program, Dept Pathol, New York, NY 10016 USA
机构:
[1] NYU, Sch Med, Mol Oncol & Immunol Program, Dept Pathol, New York, NY 10016 USA
[2] NYU, Sch Med, New York Canc Inst, New York, NY 10016 USA
基金:
美国国家卫生研究院;
关键词:
D O I:
10.1016/S0952-7915(02)00011-0
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The genes for type IIFNs(IFN-alpha and IFN-beta) are rapidly induced in response to viral infection. IFN regulatory factor (IRF) proteins are key to the regulation of IFN gene expression; the early response to virus results in secretion of a subset of IFN genes through the action of IRF3 in conjunction with additional transcription factors, such as NF-kappaB and AP-1 (c-jun-ATF2). This early IFN acts in an autocrine manner to stimulate the production of IRF7, a transcription factor capable of activating the many additional members of the IFN-alpha gene family. The dependence of IRF7 on virus-induced phosphorylation for its activity ensures that IFN production is limited to virus-infected cells. Additional members of the IRF family may provide additional levels of control, in both a cell-type and virus-specific manner, particularly in dendritic cells that serve as major producers of IFN and a key interface between innate and adaptive immunity.
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页码:52 / 58
页数:7
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