Cargando…

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,...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2021
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
_version_ 1783642351701327872
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
work_keys_str_mv AT bobrowskitesia synergisticandantagonisticdrugcombinationsagainstsarscov2
AT chenlu synergisticandantagonisticdrugcombinationsagainstsarscov2
AT eastmanrichardt synergisticandantagonisticdrugcombinationsagainstsarscov2
AT itkinzina synergisticandantagonisticdrugcombinationsagainstsarscov2
AT shinnpaul synergisticandantagonisticdrugcombinationsagainstsarscov2
AT chencatherinez synergisticandantagonisticdrugcombinationsagainstsarscov2
AT guohui synergisticandantagonisticdrugcombinationsagainstsarscov2
AT zhengwei synergisticandantagonisticdrugcombinationsagainstsarscov2
AT michaelsam synergisticandantagonisticdrugcombinationsagainstsarscov2
AT simeonovanton synergisticandantagonisticdrugcombinationsagainstsarscov2
AT hallmatthewd synergisticandantagonisticdrugcombinationsagainstsarscov2
AT zakharovalexeyv synergisticandantagonisticdrugcombinationsagainstsarscov2
AT muratoveugenen synergisticandantagonisticdrugcombinationsagainstsarscov2