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The Functional Deubiquitinating Enzymes in Control of Innate Antiviral Immunity

机译:试验抗病毒免疫控制中的功能性脱硫酶

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摘要

Innate antiviral immunity is the first line of host defense against invading viral pathogens. Immunity activation primarily relies on the recognition of pathogen‐associated molecular patterns (PAMPs) by pattern recognition receptors (PRRs). Viral proteins or nucleic acids mainly engage three classes of PRRs: Toll‐like receptors (TLRs), retinoic acid‐inducible gene I (RIG‐I)‐like receptors (RLRs), and DNA sensor cyclic GMP‐AMP (cGAMP) synthase (cGAS). These receptors initiate a series of signaling cascades that lead to the production of proinflammatory cytokines and type I interferon (IFN‐I) in response to viral infection. This system requires precise regulation to avoid aberrant activation. Emerging evidence has unveiled the crucial roles that the ubiquitin system, especially deubiquitinating enzymes (DUBs), play in controlling immune responses. In this review, an overview of the most current findings on the function of DUBs in the innate antiviral immune pathways is provided. Insights into the role of viral DUBs in counteracting host immune responses are also provided. Furthermore, the prospects and challenges of utilizing DUBs as therapeutic targets for infectious diseases are discussed.
机译:天生的抗病毒免疫是反对入侵病病原菌的第一行寄主防御。免疫激活主要依赖于通过模式识别受体(PRRS)识别病原体相关的分子模式(PAMP)。病毒蛋白或核酸主要接合三类PRRS:Toll样受体(TLR),视黄酸诱导基因I(RIG-I) - 尺寸受体(RLR)和DNA传感器环状GMP-AMP(CGAMP)合成酶( CGA)。这些受体引发了一系列信号传导级联,其​​导致促炎细胞因子和I型干扰素(IFN-1)的产生,以应对病毒感染。该系统需要精确的调节以避免异常激活。新兴的证据推出了泛素系统,尤其是脱氮酶(DUBS),在控制免疫反应中起作用的重要作用。在本次审查中,提供了在先天抗病毒免疫途径中的配音功能上的最新结果的概述。还提供了进入抵消宿主免疫反应的病毒配音的角色的见解。此外,讨论了利用配音作为传染病治疗毒性的前景和挑战。

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