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Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy?
Despite the need for novel, effective therapeutics for the COVID-19 pandemic, no curative regimen is yet available, therefore patients are forced to rely on supportive and nonspecific therapies. Some SARS-CoV-2 proteins, like the 3 C-like protease (3CLpro) or the major protease (Mpro), have been ide...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Masson SAS.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899776/ https://www.ncbi.nlm.nih.gov/pubmed/37018987 http://dx.doi.org/10.1016/j.biopha.2023.114367 |
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author | Hashemian, Seyed Mohammad Reza Sheida, Amirhossein Taghizadieh, Mohammad Memar, Mohammad Yousef Hamblin, Michael R. Bannazadeh Baghi, Hossein Sadri Nahand, Javid Asemi, Zatollah Mirzaei, Hamed |
author_facet | Hashemian, Seyed Mohammad Reza Sheida, Amirhossein Taghizadieh, Mohammad Memar, Mohammad Yousef Hamblin, Michael R. Bannazadeh Baghi, Hossein Sadri Nahand, Javid Asemi, Zatollah Mirzaei, Hamed |
author_sort | Hashemian, Seyed Mohammad Reza |
collection | PubMed |
description | Despite the need for novel, effective therapeutics for the COVID-19 pandemic, no curative regimen is yet available, therefore patients are forced to rely on supportive and nonspecific therapies. Some SARS-CoV-2 proteins, like the 3 C-like protease (3CLpro) or the major protease (Mpro), have been identified as promising targets for antiviral drugs. The Mpro has major a role in protein processing as well as pathogenesis of the virus, and could be a useful therapeutic target. The antiviral drug nirmatrelvir can keep SARS-CoV-2 from replicating through inhibiting Mpro. Nirmatrelvir was combined with another HIV protease inhibitor, ritonavir, to create Paxlovid (Nirmatrelvir/Ritonavir). The metabolizing enzyme cytochrome P450 3 A is inhibited by ritonavir to lengthen the half-life of nirmatrelvir, so rintonavir acts as a pharmacological enhancer. Nirmatrelvir exhibits potent antiviral activity against current coronavirus variants, despite significant alterations in the SARS-CoV-2 viral genome. Nevertheless, there are still several unanswered questions. This review summarizes the current literature on nirmatrelvir and ritonavir efficacy in treating SARS-CoV-2 infection, and also their safety and possible side effects. |
format | Online Article Text |
id | pubmed-9899776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Authors. Published by Elsevier Masson SAS. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98997762023-02-06 Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy? Hashemian, Seyed Mohammad Reza Sheida, Amirhossein Taghizadieh, Mohammad Memar, Mohammad Yousef Hamblin, Michael R. Bannazadeh Baghi, Hossein Sadri Nahand, Javid Asemi, Zatollah Mirzaei, Hamed Biomed Pharmacother Review Despite the need for novel, effective therapeutics for the COVID-19 pandemic, no curative regimen is yet available, therefore patients are forced to rely on supportive and nonspecific therapies. Some SARS-CoV-2 proteins, like the 3 C-like protease (3CLpro) or the major protease (Mpro), have been identified as promising targets for antiviral drugs. The Mpro has major a role in protein processing as well as pathogenesis of the virus, and could be a useful therapeutic target. The antiviral drug nirmatrelvir can keep SARS-CoV-2 from replicating through inhibiting Mpro. Nirmatrelvir was combined with another HIV protease inhibitor, ritonavir, to create Paxlovid (Nirmatrelvir/Ritonavir). The metabolizing enzyme cytochrome P450 3 A is inhibited by ritonavir to lengthen the half-life of nirmatrelvir, so rintonavir acts as a pharmacological enhancer. Nirmatrelvir exhibits potent antiviral activity against current coronavirus variants, despite significant alterations in the SARS-CoV-2 viral genome. Nevertheless, there are still several unanswered questions. This review summarizes the current literature on nirmatrelvir and ritonavir efficacy in treating SARS-CoV-2 infection, and also their safety and possible side effects. The Authors. Published by Elsevier Masson SAS. 2023-06 2023-02-06 /pmc/articles/PMC9899776/ /pubmed/37018987 http://dx.doi.org/10.1016/j.biopha.2023.114367 Text en © 2023 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Review Hashemian, Seyed Mohammad Reza Sheida, Amirhossein Taghizadieh, Mohammad Memar, Mohammad Yousef Hamblin, Michael R. Bannazadeh Baghi, Hossein Sadri Nahand, Javid Asemi, Zatollah Mirzaei, Hamed Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy? |
title | Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy? |
title_full | Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy? |
title_fullStr | Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy? |
title_full_unstemmed | Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy? |
title_short | Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy? |
title_sort | paxlovid (nirmatrelvir/ritonavir): a new approach to covid-19 therapy? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899776/ https://www.ncbi.nlm.nih.gov/pubmed/37018987 http://dx.doi.org/10.1016/j.biopha.2023.114367 |
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