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Combined Molnupiravir and Nirmatrelvir Treatment Improves the Inhibitory Effect on SARS-CoV-2 in Rhesus Macaques
The periodic emergence of SARS-CoV-2 variants of concern (VOCs) with unpredictable clinical severity and ability to escape preexisting immunity emphasizes the continued need for antiviral interventions. Two small molecule inhibitors, molnupiravir (MK-4482), a nucleoside analog, and nirmatrelvir (PF-...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cold Spring Harbor Laboratory
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580379/ https://www.ncbi.nlm.nih.gov/pubmed/36263071 http://dx.doi.org/10.1101/2022.09.03.506479 |
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author | Rosenke, Kyle Lewis, Matt C. Feldmann, Friederike Bohrnsen, Eric Schwarz, Benjamin Okumura, Atsushi Bohler, W. Forrest Callison, Julie Shaia, Carl Bosio, Catharine M. Lovaglio, Jamie Saturday, Greg Jarvis, Michael A. Feldmann, Heinz |
author_facet | Rosenke, Kyle Lewis, Matt C. Feldmann, Friederike Bohrnsen, Eric Schwarz, Benjamin Okumura, Atsushi Bohler, W. Forrest Callison, Julie Shaia, Carl Bosio, Catharine M. Lovaglio, Jamie Saturday, Greg Jarvis, Michael A. Feldmann, Heinz |
author_sort | Rosenke, Kyle |
collection | PubMed |
description | The periodic emergence of SARS-CoV-2 variants of concern (VOCs) with unpredictable clinical severity and ability to escape preexisting immunity emphasizes the continued need for antiviral interventions. Two small molecule inhibitors, molnupiravir (MK-4482), a nucleoside analog, and nirmatrelvir (PF-07321332), a 3C-like protease inhibitor, have each recently been approved as monotherapy for use in high risk COVID-19 patients. As preclinical data are only available for rodent and ferret models, we originally assessed the efficacy of MK-4482 and PF-07321332 alone and then in combination Against infection with the SARS-CoV-2 Delta VOC in the rhesus macaque COVID-19 model. Notably, use of MK-4482 and PF-07321332 in combination improved the individual inhibitory effect of both drugs. Combined treatment resulted in milder disease progression, stronger reduction of virus shedding from mucosal tissues of the upper respiratory tract, stronger reduction of viral replication in the lower respiratory tract, and reduced lung pathology. Our data strongly indicate superiority of combined MK-4482 and PF-07321332 treatment of SARS-CoV-2 infections as demonstrated here in the closest COVID-19 surrogate model. |
format | Online Article Text |
id | pubmed-9580379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-95803792022-10-20 Combined Molnupiravir and Nirmatrelvir Treatment Improves the Inhibitory Effect on SARS-CoV-2 in Rhesus Macaques Rosenke, Kyle Lewis, Matt C. Feldmann, Friederike Bohrnsen, Eric Schwarz, Benjamin Okumura, Atsushi Bohler, W. Forrest Callison, Julie Shaia, Carl Bosio, Catharine M. Lovaglio, Jamie Saturday, Greg Jarvis, Michael A. Feldmann, Heinz bioRxiv Article The periodic emergence of SARS-CoV-2 variants of concern (VOCs) with unpredictable clinical severity and ability to escape preexisting immunity emphasizes the continued need for antiviral interventions. Two small molecule inhibitors, molnupiravir (MK-4482), a nucleoside analog, and nirmatrelvir (PF-07321332), a 3C-like protease inhibitor, have each recently been approved as monotherapy for use in high risk COVID-19 patients. As preclinical data are only available for rodent and ferret models, we originally assessed the efficacy of MK-4482 and PF-07321332 alone and then in combination Against infection with the SARS-CoV-2 Delta VOC in the rhesus macaque COVID-19 model. Notably, use of MK-4482 and PF-07321332 in combination improved the individual inhibitory effect of both drugs. Combined treatment resulted in milder disease progression, stronger reduction of virus shedding from mucosal tissues of the upper respiratory tract, stronger reduction of viral replication in the lower respiratory tract, and reduced lung pathology. Our data strongly indicate superiority of combined MK-4482 and PF-07321332 treatment of SARS-CoV-2 infections as demonstrated here in the closest COVID-19 surrogate model. Cold Spring Harbor Laboratory 2022-09-05 /pmc/articles/PMC9580379/ /pubmed/36263071 http://dx.doi.org/10.1101/2022.09.03.506479 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Rosenke, Kyle Lewis, Matt C. Feldmann, Friederike Bohrnsen, Eric Schwarz, Benjamin Okumura, Atsushi Bohler, W. Forrest Callison, Julie Shaia, Carl Bosio, Catharine M. Lovaglio, Jamie Saturday, Greg Jarvis, Michael A. Feldmann, Heinz Combined Molnupiravir and Nirmatrelvir Treatment Improves the Inhibitory Effect on SARS-CoV-2 in Rhesus Macaques |
title | Combined Molnupiravir and Nirmatrelvir Treatment Improves the Inhibitory Effect on SARS-CoV-2 in Rhesus Macaques |
title_full | Combined Molnupiravir and Nirmatrelvir Treatment Improves the Inhibitory Effect on SARS-CoV-2 in Rhesus Macaques |
title_fullStr | Combined Molnupiravir and Nirmatrelvir Treatment Improves the Inhibitory Effect on SARS-CoV-2 in Rhesus Macaques |
title_full_unstemmed | Combined Molnupiravir and Nirmatrelvir Treatment Improves the Inhibitory Effect on SARS-CoV-2 in Rhesus Macaques |
title_short | Combined Molnupiravir and Nirmatrelvir Treatment Improves the Inhibitory Effect on SARS-CoV-2 in Rhesus Macaques |
title_sort | combined molnupiravir and nirmatrelvir treatment improves the inhibitory effect on sars-cov-2 in rhesus macaques |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580379/ https://www.ncbi.nlm.nih.gov/pubmed/36263071 http://dx.doi.org/10.1101/2022.09.03.506479 |
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