Lo Ho Sing, Hui Kenrie Pui Yan, Lai Hei-Ming, He Xu, Khan Khadija Shahed, Kaur Simranjeet, Huang Junzhe, Li Zhongqi, Chan Anthony K N, Cheung Hayley Hei-Yin, Ng Ka-Chun, Ho John Chi Wang, Chen Yu Wai, Ma Bowen, Cheung Peter Man-Hin, Shin Donghyuk, Wang Kaidao, Lee Meng-Hsuan, Selisko Barbara, Eydoux Cecilia, Guillemot Jean-Claude, Canard Bruno, Wu Kuen-Phon, Liang Po-Huang, Dikic Ivan, Zuo Zhong, Chan Francis K L, Hui David S C, Mok Vincent C T, Wong Kam-Bo, Mok Chris Ka Pun, Ko Ho, Aik Wei Shen, Chan Michael Chi Wai, Ng Wai-Lung
School of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, Hong Kong.
School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong.
ACS Cent Sci. 2021 May 26;7(5):792-802. doi: 10.1021/acscentsci.0c01186. Epub 2021 Apr 15.
The outbreak of coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is a global threat to human health. Using a multidisciplinary approach, we identified and validated the hepatitis C virus (HCV) protease inhibitor simeprevir as an especially promising repurposable drug for treating COVID-19. Simeprevir potently reduces SARS-CoV-2 viral load by multiple orders of magnitude and synergizes with remdesivir . Mechanistically, we showed that simeprevir not only inhibits the main protease (M) and unexpectedly the RNA-dependent RNA polymerase (RdRp) but also modulates host immune responses. Our results thus reveal the possible anti-SARS-CoV-2 mechanism of simeprevir and highlight the translational potential of optimizing simeprevir as a therapeutic agent for managing COVID-19 and future outbreaks of CoV.
由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病(COVID-19)疫情是对人类健康的全球性威胁。我们采用多学科方法,鉴定并验证了丙型肝炎病毒(HCV)蛋白酶抑制剂西米普明是一种特别有前景的可用于治疗COVID-19的可重新利用药物。西米普明能将SARS-CoV-2病毒载量有效降低多个数量级,并与瑞德西韦协同作用。从机制上讲,我们表明西米普明不仅抑制主要蛋白酶(M),而且意外地抑制RNA依赖性RNA聚合酶(RdRp),还能调节宿主免疫反应。因此,我们的结果揭示了西米普明可能的抗SARS-CoV-2机制,并突出了优化西米普明作为治疗COVID-19及未来冠状病毒爆发的治疗剂的转化潜力。