I型干扰素系统的信号转导及病毒对策。

Signal transduction Pub Date : 2007-02-01 Epub Date: 2007-02-02 DOI:10.1002/sita.200600115
Krzysztof Brzózka, Christian Pfaller, Karl-Klaus Conzelmann
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引用次数: 8

摘要

I型干扰素(IFN)包括IFNα/β是免疫系统的细胞因子,在先天和适应性免疫反应中具有重要功能。分泌的IFN通过JAK/STAT信号通路指导一个庞大的基因表达程序,包括抗病毒、凋亡、生存和免疫基因。直到最近,导致IFN基因转录激活的分子模式及其受体以及相关的信号通路才被阐明。无处不在的胞质RNA解旋酶,如RIG-I,可感知细胞内三磷酸RNA并激活ifn控制转录因子IRF3和IRF7,似乎在抗病毒防御和免疫中发挥重要作用。另外,toll样受体子集对细胞外核酸的识别有助于宿主IFN的普遍反应。在与宿主共同进化的过程中,病毒已经学会了对抗干扰素网络的每一部分。从病毒中学习如何靶向IFN系统可能会给我们带来新的治疗干预策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Signal transduction in the type I interferon system and viral countermeasures.

Type I interferons (IFN) including IFNα/β are cytokines of the immune system with critical functions in innate and adaptive immune response. Secreted IFN acts via JAK/STAT signaling pathways to direct a huge gene expression program, including antiviral, apoptotic, survival and immune genes. Only recently, the molecular patterns and their receptors as well as the connected signaling pathways leading to transcriptional activation of IFN genes have been elucidated. Ubiquitous cytosolic RNA helicases like RIG-I which sense intracellular triphosphate RNAs and activate the IFN-controlling transcription factors IRF3 and IRF7 seem to play a major role in antiviral defense and immunity. Recognition of extracellular nucleic acids by a subset of Toll-like receptors in addition contributes to a generalized host IFN response. During co-evolution with the host, viruses have learned to counteract every piece of the IFN network. Learning from viruses how to target the IFN system may lead us to novel strategies for therapeutic intervention.

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