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Synergistic and Antagonistic Drug Combinations against SARS-CoV-2
Antiviral drug development for coronavirus disease 2019 (COVID-19) is occurring at an unprecedented pace, yet there are still limited therapeutic options for treating this disease. We hypothesized that combining drugs with independent mechanisms of action could result in synergy against SARS-CoV-2,...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7834738/ https://www.ncbi.nlm.nih.gov/pubmed/33333292 http://dx.doi.org/10.1016/j.ymthe.2020.12.016 |
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author | Bobrowski, Tesia Chen, Lu Eastman, Richard T. Itkin, Zina Shinn, Paul Chen, Catherine Z. Guo, Hui Zheng, Wei Michael, Sam Simeonov, Anton Hall, Matthew D. Zakharov, Alexey V. Muratov, Eugene N. |
author_facet | Bobrowski, Tesia Chen, Lu Eastman, Richard T. Itkin, Zina Shinn, Paul Chen, Catherine Z. Guo, Hui Zheng, Wei Michael, Sam Simeonov, Anton Hall, Matthew D. Zakharov, Alexey V. Muratov, Eugene N. |
author_sort | Bobrowski, Tesia |
collection | PubMed |
description | Antiviral drug development for coronavirus disease 2019 (COVID-19) is occurring at an unprecedented pace, yet there are still limited therapeutic options for treating this disease. We hypothesized that combining drugs with independent mechanisms of action could result in synergy against SARS-CoV-2, thus generating better antiviral efficacy. Using in silico approaches, we prioritized 73 combinations of 32 drugs with potential activity against SARS-CoV-2 and then tested them in vitro. Sixteen synergistic and eight antagonistic combinations were identified; among 16 synergistic cases, combinations of the US Food and Drug Administration (FDA)-approved drug nitazoxanide with remdesivir, amodiaquine, or umifenovir were most notable, all exhibiting significant synergy against SARS-CoV-2 in a cell model. However, the combination of remdesivir and lysosomotropic drugs, such as hydroxychloroquine, demonstrated strong antagonism. Overall, these results highlight the utility of drug repurposing and preclinical testing of drug combinations for discovering potential therapies to treat COVID-19. |
format | Online Article Text |
id | pubmed-7834738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-78347382021-01-26 Synergistic and Antagonistic Drug Combinations against SARS-CoV-2 Bobrowski, Tesia Chen, Lu Eastman, Richard T. Itkin, Zina Shinn, Paul Chen, Catherine Z. Guo, Hui Zheng, Wei Michael, Sam Simeonov, Anton Hall, Matthew D. Zakharov, Alexey V. Muratov, Eugene N. Mol Ther Original Article Antiviral drug development for coronavirus disease 2019 (COVID-19) is occurring at an unprecedented pace, yet there are still limited therapeutic options for treating this disease. We hypothesized that combining drugs with independent mechanisms of action could result in synergy against SARS-CoV-2, thus generating better antiviral efficacy. Using in silico approaches, we prioritized 73 combinations of 32 drugs with potential activity against SARS-CoV-2 and then tested them in vitro. Sixteen synergistic and eight antagonistic combinations were identified; among 16 synergistic cases, combinations of the US Food and Drug Administration (FDA)-approved drug nitazoxanide with remdesivir, amodiaquine, or umifenovir were most notable, all exhibiting significant synergy against SARS-CoV-2 in a cell model. However, the combination of remdesivir and lysosomotropic drugs, such as hydroxychloroquine, demonstrated strong antagonism. Overall, these results highlight the utility of drug repurposing and preclinical testing of drug combinations for discovering potential therapies to treat COVID-19. American Society of Gene & Cell Therapy 2021-02-03 2020-12-15 /pmc/articles/PMC7834738/ /pubmed/33333292 http://dx.doi.org/10.1016/j.ymthe.2020.12.016 Text en © 2020 The American Society of Gene and Cell Therapy. |
spellingShingle | Original Article Bobrowski, Tesia Chen, Lu Eastman, Richard T. Itkin, Zina Shinn, Paul Chen, Catherine Z. Guo, Hui Zheng, Wei Michael, Sam Simeonov, Anton Hall, Matthew D. Zakharov, Alexey V. Muratov, Eugene N. Synergistic and Antagonistic Drug Combinations against SARS-CoV-2 |
title | Synergistic and Antagonistic Drug Combinations against SARS-CoV-2 |
title_full | Synergistic and Antagonistic Drug Combinations against SARS-CoV-2 |
title_fullStr | Synergistic and Antagonistic Drug Combinations against SARS-CoV-2 |
title_full_unstemmed | Synergistic and Antagonistic Drug Combinations against SARS-CoV-2 |
title_short | Synergistic and Antagonistic Drug Combinations against SARS-CoV-2 |
title_sort | synergistic and antagonistic drug combinations against sars-cov-2 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7834738/ https://www.ncbi.nlm.nih.gov/pubmed/33333292 http://dx.doi.org/10.1016/j.ymthe.2020.12.016 |
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