Dynamic control of type I IFN signalling by an integrated network of negative regulators

被引:169
作者
Porritt, Rebecca A. [1 ]
Hertzog, Paul J.
机构
[1] Monash Univ, MIMR PHI, Ctr Innate Immun & Infect Dis, Clayton, Vic 3068, Australia
关键词
Interferon; cytokine; STAT; JAK; SOCS; NF-KAPPA-B; PROTEIN-TYROSINE-PHOSPHATASE; DOUBLE-STRANDED-RNA; INTERFERON-BETA; IMMUNE-RESPONSE; ANTIVIRAL RESPONSE; GENE-ACTIVATION; INDUCIBLE GENE; SOCS; UBIQUITIN;
D O I
10.1016/j.it.2015.02.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Whereas type I interferons (IFNs) have critical roles in protection from pathogens, excessive IFN responses contribute to pathology in both acute and chronic settings, pointing to the importance of balancing activating signals with regulatory mechanisms that appropriately tune the response. Here we review evidence for an integrated network of negative regulators of IFN production and action, which function at all levels of. the activating and effector signalling pathways. We propose that the aim of this extensive network is to limit tissue damage while enabling an IFN response that is temporally appropriate and of sufficient magnitude. Understanding the architecture and dynamics of this network, and how it differs in distinct tissues, will provide new insights into IFN biology and aid the design of more effective therapeutics.
引用
收藏
页码:150 / 160
页数:11
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