1] Arthritis and Tissue Degeneration Program and the David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, New York 10021, USA. [2] Immunology and Microbial Pathogenesis Program, Weill Cornell Graduate School of Medical Sciences, New York, New York 10065, USA. [3] Department of Medicine, Weill Cornell Medical College, New York, New York 10065,USA.
Arthritis and Tissue Degeneration Program and the David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, New York 10021, USA.
Nat Rev Immunol. 2014 Jan;14(1):36-49. doi: 10.1038/nri3581.
Type I interferons (IFNs) activate intracellular antimicrobial programmes and influence the development of innate and adaptive immune responses. Canonical type I IFN signalling activates the Janus kinase (JAK)-signal transducer and activator of transcription (STAT) pathway, leading to transcription of IFN-stimulated genes (ISGs). Host, pathogen and environmental factors regulate the responses of cells to this signalling pathway and thus calibrate host defences while limiting tissue damage and preventing autoimmunity. Here, we summarize the signalling and epigenetic mechanisms that regulate type I IFN-induced STAT activation and ISG transcription and translation. These regulatory mechanisms determine the biological outcomes of type I IFN responses and whether pathogens are cleared effectively or chronic infection or autoimmune disease ensues.
I 型干扰素 (IFNs) 激活细胞内抗菌程序,并影响先天和适应性免疫反应的发展。经典的 I 型 IFN 信号激活 Janus 激酶 (JAK)-信号转导和转录激活因子 (STAT) 途径,导致 IFN 刺激基因 (ISGs) 的转录。宿主、病原体和环境因素调节细胞对这种信号通路的反应,从而在限制组织损伤和预防自身免疫的同时,调节宿主防御。在这里,我们总结了调节 I 型 IFN 诱导的 STAT 激活和 ISG 转录和翻译的信号和表观遗传机制。这些调节机制决定了 I 型 IFN 反应的生物学结果,以及病原体是否被有效清除,还是会导致慢性感染或自身免疫性疾病。