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RIG-I 和 MDA5 的治疗靶向作用可能不会导致相同的结果。

Therapeutic Targeting of RIG-I and MDA5 Might Not Lead to the Same Rome.

机构信息

Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada; Department of Biochemistry and Molecular Medicine, Faculty of Medicine, Université de Montréal, Montréal, QC, Canada.

Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada; Department of Biochemistry and Molecular Medicine, Faculty of Medicine, Université de Montréal, Montréal, QC, Canada.

出版信息

Trends Pharmacol Sci. 2019 Feb;40(2):116-127. doi: 10.1016/j.tips.2018.12.003. Epub 2018 Dec 31.

Abstract

RIG-I and MDA5 receptors are key sensors of pathogen-associated molecular pattern (PAMP)-containing viral RNA and transduce downstream signals to activate an antiviral and immunomodulatory response. Fifteen years of research have put them at the center of an ongoing hunt for novel pharmacological pan-antivirals, vaccine adjuvants, and antitumor strategies. Current knowledge testifies to the redundant, but also distinct, functions mediated by RIG-I and MDA5, opening opportunities for the use of specific and potent nucleic acid agonists. We critically discuss the evidence and remaining knowledge gaps that have an impact on the choice and design of optimal RNA ligands to achieve an appropriate immunostimulatory response, with limited adverse effects, for prophylactic and therapeutic interventions against viruses and cancer in humans.

摘要

RIG-I 和 MDA5 受体是识别病原体相关分子模式(PAMP)包含的病毒 RNA 的关键传感器,并传递下游信号以激活抗病毒和免疫调节反应。十五年的研究使它们成为新型广谱抗病毒药物、疫苗佐剂和抗肿瘤策略的研究热点。目前的知识证明了 RIG-I 和 MDA5 介导的冗余但又独特的功能,为使用特定有效的核酸激动剂提供了机会。我们批判性地讨论了对选择和设计最佳 RNA 配体以实现适当的免疫刺激反应的影响,同时限制不良反应,用于预防和治疗人类病毒和癌症的证据和遗留知识空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ce/7112877/b592b0155246/gr1_lrg.jpg

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