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Potential therapeutics for SARS

Reactome ID: R-HSA-9679191

中文名称

TBK1、IKKε介导的IRF3、IRF7激活的调控

通路描述

Toll样受体3(TLR3)和TLR4配体诱导的I型干扰素基因的产生由TBK1或IKKε(IKBKE)介导,它们磷酸化干扰素调节因子3(IRF3)和IRF7。TBK1和/或IRF3、IRF7的活动受多种机制调节,包括翻译后修饰、蛋白质相互作用和蛋白质降解(Zhao W等,2013;Runde AP等,2022)。
本Reactome模块描述了TBK1和IKKε活性通过K63连接泛素化以及TBK1与OPTN相互作用而受到调节。
英文描述
Potential therapeutics for SARS The search for drugs to prevent or reduce the severity of human infection with SARS-CoV-1 or SARS-CoV-2 has centered on ones that are effective in treatment of human infections with other RNA viruses or in diminishing cytokine storms and other pathologies due to destructive host reactions. The interactions of a large number of these candidate drugs with their known viral and human protein targets are annotated, as are some drugs that inhibit Cytochrome P450 (CYP) oxidoreductases to prolong the plasma half-lives of antiviral drugs. In addition, effects of these drugs on unrelated essential human proteins, that might limit their use in vivo, are annotated.A notable success of this search is a combination treatment, Paxlovid (NCT04960202), involving ritonavir, an inhibitor of CYP3A4 and CYP2B6 oxidoreductases, and nirmatrelvir, an inhibitor of SARS-CoV-2 3CLp protease, to block steps in maturation of viral replicase proteins (Hashemian et al. 2023).

所含基因

108 个基因