Simeprevir Potently Suppresses SARS-CoV-2 Replication and Synergizes with Remdesivir

西美普韦能有效抑制SARS-CoV-2复制,并与瑞德西韦产生协同作用

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作者:Ho Sing Lo,Kenrie Pui Yan Hui,Hei-Ming Lai,Xu He,Khadija Shahed Khan,Simranjeet Kaur,Junzhe Huang,Zhongqi Li,Anthony K N Chan,Hayley Hei-Yin Cheung,Ka-Chun Ng,John Chi Wang Ho,Yu Wai Chen,Bowen Ma,Peter Man-Hin Cheung,Donghyuk Shin,Kaidao Wang,Meng-Hsuan Lee,Barbara Selisko,Cecilia Eydoux,Jean-Claude Guillemot,Bruno Canard,Kuen-Phon Wu,Po-Huang Liang,Ivan Dikic,Zhong Zuo,Francis K L Chan,David S C Hui,Vincent C T Mok,Kam-Bo Wong,Chris Ka Pun Mok,Ho Ko,Wei Shen Aik,Michael Chi Wai Chan,Wai-Lung Ng

Abstract

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.

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