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- Publisher Website: 10.1021/acscentsci.0c01186
- Scopus: eid_2-s2.0-85105116950
- PMID: 34075346
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Article: Simeprevir Potently Suppresses SARS-CoV-2 Replication and Synergizes with Remdesivir
Title | Simeprevir Potently Suppresses SARS-CoV-2 Replication and Synergizes with Remdesivir |
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Authors | |
Issue Date | 2021 |
Publisher | American Chemical Society: Open Access Titles. The Journal's web site is located at http://pubs.acs.org/journal/acscii |
Citation | ACS Central Science, 2021, v. 7 n. 5, p. 792-802 How to Cite? |
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. |
Persistent Identifier | http://hdl.handle.net/10722/305184 |
ISSN | 2023 Impact Factor: 12.7 2023 SCImago Journal Rankings: 3.722 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Lo, HS | - |
dc.contributor.author | Hui, KPY | - |
dc.contributor.author | Lai, HM | - |
dc.contributor.author | He, X | - |
dc.contributor.author | Khan, KS | - |
dc.contributor.author | Kaur, S | - |
dc.contributor.author | Huang, J | - |
dc.contributor.author | Li, Z | - |
dc.contributor.author | Chan, AKN | - |
dc.contributor.author | Cheung, HHY | - |
dc.contributor.author | Ng, KC | - |
dc.contributor.author | Ho, JCW | - |
dc.contributor.author | Chen, YW | - |
dc.contributor.author | Ma, B | - |
dc.contributor.author | Cheung, PMH | - |
dc.contributor.author | Shin, D | - |
dc.contributor.author | Wang, K | - |
dc.contributor.author | Lee, MH | - |
dc.contributor.author | Selisko, B | - |
dc.contributor.author | Eydoux, C | - |
dc.contributor.author | Guillemot, JC | - |
dc.contributor.author | Canard, B | - |
dc.contributor.author | Wu, KP | - |
dc.contributor.author | Liang, PH | - |
dc.contributor.author | Dikic, I | - |
dc.contributor.author | Zuo, Z | - |
dc.contributor.author | Chan, FK | - |
dc.contributor.author | Hui, DSC | - |
dc.contributor.author | Mok, VC | - |
dc.contributor.author | Wong, KB | - |
dc.contributor.author | Mok, CKP | - |
dc.contributor.author | Ko, H | - |
dc.contributor.author | Aik, WS | - |
dc.contributor.author | Chan, MCW | - |
dc.contributor.author | Ng, WL | - |
dc.date.accessioned | 2021-10-20T10:05:48Z | - |
dc.date.available | 2021-10-20T10:05:48Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | ACS Central Science, 2021, v. 7 n. 5, p. 792-802 | - |
dc.identifier.issn | 2374-7951 | - |
dc.identifier.uri | http://hdl.handle.net/10722/305184 | - |
dc.description.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. | - |
dc.language | eng | - |
dc.publisher | American Chemical Society: Open Access Titles. The Journal's web site is located at http://pubs.acs.org/journal/acscii | - |
dc.relation.ispartof | ACS Central Science | - |
dc.rights | This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes. | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | Simeprevir Potently Suppresses SARS-CoV-2 Replication and Synergizes with Remdesivir | - |
dc.type | Article | - |
dc.identifier.email | Hui, KPY: kenrie@hku.hk | - |
dc.identifier.email | Ng, KC: kckachun@hku.hk | - |
dc.identifier.email | Ho, JCW: cwjohn@connect.hku.hk | - |
dc.identifier.email | Chan, MCW: mchan@hku.hk | - |
dc.identifier.authority | Hui, KPY=rp02149 | - |
dc.identifier.authority | Chan, MCW=rp00420 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1021/acscentsci.0c01186 | - |
dc.identifier.pmid | 34075346 | - |
dc.identifier.pmcid | PMC8056950 | - |
dc.identifier.scopus | eid_2-s2.0-85105116950 | - |
dc.identifier.hkuros | 327760 | - |
dc.identifier.volume | 7 | - |
dc.identifier.issue | 5 | - |
dc.identifier.spage | 792 | - |
dc.identifier.epage | 802 | - |
dc.identifier.isi | WOS:000657243600013 | - |
dc.publisher.place | United States | - |