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非甾体抗炎药萘普生靶向 SARS-CoV-2 冠状病毒核蛋白的抗病毒特性。

Antiviral Properties of the NSAID Drug Naproxen Targeting the Nucleoprotein of SARS-CoV-2 Coronavirus.

机构信息

CIRI, Centre International de Recherche en Infectiologie, (Team VirPath), Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007 Lyon, France.

Cancer Biology and Therapeutics Team, INSERM, UMR_S 938, Centre de Recherche Saint-Antoine, Sorbonne Universitè, F-75012 Paris, France.

出版信息

Molecules. 2021 Apr 29;26(9):2593. doi: 10.3390/molecules26092593.

Abstract

There is an urgent need for specific antiviral treatments directed against SARS-CoV-2 to prevent the most severe forms of COVID-19. By drug repurposing, affordable therapeutics could be supplied worldwide in the present pandemic context. Targeting the nucleoprotein N of the SARS-CoV-2 coronavirus could be a strategy to impede viral replication and possibly other essential functions associated with viral N. The antiviral properties of naproxen, a non-steroidal anti-inflammatory drug (NSAID) that was previously demonstrated to be active against Influenza A virus, were evaluated against SARS-CoV-2. Intrinsic fluorescence spectroscopy, fluorescence anisotropy, and dynamic light scattering assays demonstrated naproxen binding to the nucleoprotein of SARS-Cov-2 as predicted by molecular modeling. Naproxen impeded recombinant N oligomerization and inhibited viral replication in infected cells. In VeroE6 cells and reconstituted human primary respiratory epithelium models of SARS-CoV-2 infection, naproxen specifically inhibited viral replication and protected the bronchial epithelia against SARS-CoV-2-induced damage. No inhibition of viral replication was observed with paracetamol or the COX-2 inhibitor celecoxib. Thus, among the NSAID tested, only naproxen combined antiviral and anti-inflammatory properties. Naproxen addition to the standard of care could be beneficial in a clinical setting, as tested in an ongoing clinical study.

摘要

目前正处于大流行时期,急需针对 SARS-CoV-2 的特定抗病毒疗法来预防 COVID-19 的最严重形式。通过药物再利用,可以在当前大流行背景下向全球提供负担得起的治疗方法。针对 SARS-CoV-2 冠状病毒核衣壳蛋白 N 可能是一种阻碍病毒复制并可能阻碍与病毒 N 相关的其他基本功能的策略。先前证明具有抗甲型流感病毒活性的非甾体抗炎药(NSAID)萘普生的抗病毒特性针对 SARS-CoV-2 进行了评估。本研究通过内源荧光光谱、荧光各向异性和动态光散射实验证明了萘普生与 SARS-Cov-2 核衣壳蛋白的结合,这与分子建模预测的结果一致。萘普生阻碍了重组 N 寡聚化并抑制了感染细胞中的病毒复制。在感染 SARS-CoV-2 的 VeroE6 细胞和重建的人原代呼吸道上皮细胞模型中,萘普生特异性抑制病毒复制并保护支气管上皮免受 SARS-CoV-2 诱导的损伤。扑热息痛或 COX-2 抑制剂塞来昔布均未观察到抑制病毒复制的作用。因此,在所测试的 NSAID 中,只有萘普生兼具抗病毒和抗炎特性。在一项正在进行的临床研究中,萘普生可与标准治疗方法联合使用,这可能对临床有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6afb/8124269/4eda756d2eff/molecules-26-02593-g001.jpg

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