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Remdesivir and Its Combination With Repurposed Drugs as COVID-19 Therapeutics
The SARS-CoV-2 virus needs multiple copies for its multiplication using an enzyme RNA-dependent RNA polymerase (RdRp). Remdesivir inhibits viral RdRp, controls the multiplication of the virus, and protects patients. However, treatment of COVID-19 with remdesivir involves adverse effects. Many ongoin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134007/ https://www.ncbi.nlm.nih.gov/pubmed/35634324 http://dx.doi.org/10.3389/fimmu.2022.830990 |
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author | Chatterjee, Bhaswati Thakur, Suman S. |
author_facet | Chatterjee, Bhaswati Thakur, Suman S. |
author_sort | Chatterjee, Bhaswati |
collection | PubMed |
description | The SARS-CoV-2 virus needs multiple copies for its multiplication using an enzyme RNA-dependent RNA polymerase (RdRp). Remdesivir inhibits viral RdRp, controls the multiplication of the virus, and protects patients. However, treatment of COVID-19 with remdesivir involves adverse effects. Many ongoing clinical trials are exploring the potential of the combination of remdesivir with repurposed drugs by targeting multiple targets of virus and host human simultaneously. Better results were obtained with the remdesivir–baricitinib combination treatment for COVID-19 compared to the treatment with remdesivir alone. Notably, recovery from COVID-19 was found to be 8 days less via the remdesivir–baricitinib combination treatment as compared to remdesivir treatment alone. Furthermore, the mortality rate via the remdesivir–baricitinib combination treatment was lower compared to the remdesivir-only treatment. Remdesivir targets the SARS-CoV-2 enzyme while baricitinib targets the host human enzyme. Simultaneously, remdesivir and baricitinib as a combination inhibit their target viral RdRp and human Janus kinase, respectively. Ongoing trials for the combination of drugs will suggest in the future whether they may reduce the recovery time, reduce the mortality rate, and improve patient clinical status for noninvasive ventilation. In the future, simultaneously targeting virus replication enzymes and host human kinases may be the strategy for SARS-CoV-2 therapeutics. |
format | Online Article Text |
id | pubmed-9134007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91340072022-05-27 Remdesivir and Its Combination With Repurposed Drugs as COVID-19 Therapeutics Chatterjee, Bhaswati Thakur, Suman S. Front Immunol Immunology The SARS-CoV-2 virus needs multiple copies for its multiplication using an enzyme RNA-dependent RNA polymerase (RdRp). Remdesivir inhibits viral RdRp, controls the multiplication of the virus, and protects patients. However, treatment of COVID-19 with remdesivir involves adverse effects. Many ongoing clinical trials are exploring the potential of the combination of remdesivir with repurposed drugs by targeting multiple targets of virus and host human simultaneously. Better results were obtained with the remdesivir–baricitinib combination treatment for COVID-19 compared to the treatment with remdesivir alone. Notably, recovery from COVID-19 was found to be 8 days less via the remdesivir–baricitinib combination treatment as compared to remdesivir treatment alone. Furthermore, the mortality rate via the remdesivir–baricitinib combination treatment was lower compared to the remdesivir-only treatment. Remdesivir targets the SARS-CoV-2 enzyme while baricitinib targets the host human enzyme. Simultaneously, remdesivir and baricitinib as a combination inhibit their target viral RdRp and human Janus kinase, respectively. Ongoing trials for the combination of drugs will suggest in the future whether they may reduce the recovery time, reduce the mortality rate, and improve patient clinical status for noninvasive ventilation. In the future, simultaneously targeting virus replication enzymes and host human kinases may be the strategy for SARS-CoV-2 therapeutics. Frontiers Media S.A. 2022-05-12 /pmc/articles/PMC9134007/ /pubmed/35634324 http://dx.doi.org/10.3389/fimmu.2022.830990 Text en Copyright © 2022 Chatterjee and Thakur https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Chatterjee, Bhaswati Thakur, Suman S. Remdesivir and Its Combination With Repurposed Drugs as COVID-19 Therapeutics |
title | Remdesivir and Its Combination With Repurposed Drugs as COVID-19 Therapeutics |
title_full | Remdesivir and Its Combination With Repurposed Drugs as COVID-19 Therapeutics |
title_fullStr | Remdesivir and Its Combination With Repurposed Drugs as COVID-19 Therapeutics |
title_full_unstemmed | Remdesivir and Its Combination With Repurposed Drugs as COVID-19 Therapeutics |
title_short | Remdesivir and Its Combination With Repurposed Drugs as COVID-19 Therapeutics |
title_sort | remdesivir and its combination with repurposed drugs as covid-19 therapeutics |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134007/ https://www.ncbi.nlm.nih.gov/pubmed/35634324 http://dx.doi.org/10.3389/fimmu.2022.830990 |
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