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Manipulation of the nuclear factor-|[kappa]|B pathway and the innate immune response by viruses

机译:操纵核因子-|κ| B途径和病毒的先天免疫应答

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Viral and microbial constituents contain specific motifs or pathogen-associated molecular patterns (PAMPs) that are recognized by cell surface- and endosome-associated Toll-like receptors (TLRs). In addition, intracellular viral double-stranded RNA is detected by two recently characterized DExD/H box RNA helicases, RIG-I and Mda-5. Both TLR-dependent and -independent pathways engage the IB kinase (IKK) complex and related kinases TBK-1 and IKK. Activation of the nuclear factor B (NF-B) and interferon regulatory factor (IRF) transcription factor pathways are essential immediate early steps of immune activation; as a result, both pathways represent prime candidates for viral interference. Many viruses have developed strategies to manipulate NF-B signaling through the use of multifunctional viral proteins that target the host innate immune response pathways. This review discusses three rapidly evolving areas of research on viral pathogenesis: the recognition and signaling in response to virus infection through TLR-dependent and -independent mechanisms, the involvement of NF-B in the host innate immune response and the multitude of strategies used by different viruses to short circuit the NF-B pathway.
机译:病毒和微生物成分包含被细胞表面和内体相关的Toll样受体(TLR)识别的特定基序或病原体相关的分子模式(PAMP)。另外,细胞内病毒双链RNA被两个最近表征的DExD / H盒RNA解旋酶RIG-1和Mda-5检测到。 TLR依赖性和非依赖性途径均参与IB激酶(IKK)复合物和相关激酶TBK-1和IKK。核因子B(NF-B)和干扰素调节因子(IRF)转录因子途径的激活是免疫激活的重要基础。结果,这两种途径都代表了病毒干扰的主要候选者。许多病毒已经开发出通过使用靶向宿主固有免疫应答途径的多功能病毒蛋白来操纵NF-B信号的策略。这篇综述讨论了病毒发病机理研究的三个快速发展的领域:通过TLR依赖性和非依赖性机制识别和响应病毒感染的信号,NF-B在宿主固有免疫反应中的参与以及病毒所使用的多种策略。不同的病毒会短路NF-B通路。

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