Simeprevir Potently Suppresses SARS-CoV-2 Replication and Synergizes with Remdesivir.
Ho Sing LoKenrie Pui Yan HuiHei-Ming LaiXu HeKhadija Shahed KhanSimranjeet KaurJunzhe HuangZhongqi LiAnthony K C ChanHayley Hei-Yin CheungKa-Chun NgJohn Chi Wang HoYu Wai ChenBowen MaPeter Man-Hin CheungDonghyuk ShinKaidao WangMeng-Hsuan LeeBarbara SeliskoCecilia EydouxJean-Claude GuillemotBruno CanardKuen-Phon WuPo-Huang LiangIvan ĐikićZhong ZuoFrancis K L ChanDavid S C HuiVincent C T MokKam-Bo WongChris Ka Pun MokHo KoWei Shen AikMichael Chi Wai ChanBilly Wai-Lung NgPublished in: ACS central science (2021)
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 in vitro. Mechanistically, we showed that simeprevir not only inhibits the main protease (Mpro) 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.