Repurposing Drugs and Synergistic Combinations as Potential Therapies for Inhibiting SARS-CoV-2 and Coronavirus Replication

Drug repurposing can serve an important role in rapidly discovering medicament options for emerging microbial pandemics. In this study, a pragmatic approach is demonstrated for screening and testing drug combinations as potential broad-spectrum therapies against SARS-CoV-2 and other betacoronaviruses. Rapid cell-based phenotypic small molecule screens were executed using related common-cold-causing HCoV-OC43 betacoronavirus to identify replication inhibitors from a library of drugs approved by regulatory agencies for other indications. Given the best inhibitors, an expedient checkerboard strategy then served to identify synergistic drug combinations. These combinations were then validated using more challenging assays involving SARS-CoV-2 and variants. Promising drug combinations against multiple viral variants were discovered and involved Tilorone with Nelfinavir or Molnupiravir.

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Publication Details

Journal
ACS Pharmacology & Translational Science
Published
2024-11-05
DOI
https://doi.org/10.1021/acsptsci.4c00512
Citations
1
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
0.39

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Repurposing Drugs and Synergistic Combinations as Potential Therapies for Inhibiting SARS-CoV-2 and Coronavirus Replication

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Repurposing Drugs and Synergistic Combinations as Potential Therapies for Inhibiting SARS-CoV-2 and Coronavirus Replication

Tania Charpentier, Anaïs Anton, Laurent Chatel‐Chaix, Richard Boulon, Steven R. LaPlante, Majid D. Farahani, Alain Lamarre, Yann Ayotte, Clément Mazeaud, Mustapha Iddir, Simon Woo, Mathilde Broquière
article en
1 citations

Abstract

Drug repurposing can serve an important role in rapidly discovering medicament options for emerging microbial pandemics. In this study, a pragmatic approach is demonstrated for screening and testing drug combinations as potential broad-spectrum therapies against SARS-CoV-2 and other betacoronaviruses. Rapid cell-based phenotypic small molecule screens were executed using related common-cold-causing HCoV-OC43 betacoronavirus to identify replication inhibitors from a library of drugs approved by regulatory agencies for other indications. Given the best inhibitors, an expedient checkerboard strategy then served to identify synergistic drug combinations. These combinations were then validated using more challenging assays involving SARS-CoV-2 and variants. Promising drug combinations against multiple viral variants were discovered and involved Tilorone with Nelfinavir or Molnupiravir.

ACS Pharmacology & Translational ScienceVol. 7(12)
Institut National de la Recherche Scientifique (CA)
Armand-Frappier Foundation, Institut national de la recherche scientifique, Québec Consortium for Drug Discovery, Institut Pasteur, Mitacs, Fonds de Recherche du Québec - Santé
Good health and well-being
Openalex Percentile: Top 35%
SARS-CoV-2 and COVID-19 Research
0.39
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