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Nirmatrelvir treatment of SARS‐CoV‐2‐infected mice blunts antiviral adaptive immune responses

Alongside vaccines, antiviral drugs are becoming an integral part of our response to the SARS‐CoV‐2 pandemic. Nirmatrelvir—an orally available inhibitor of the 3‐chymotrypsin‐like cysteine protease—has been shown to reduce the risk of progression to severe COVID‐19. However, the impact of nirmatrelv...

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Autores principales: Fumagalli, Valeria, Di Lucia, Pietro, Ravà, Micol, Marotta, Davide, Bono, Elisa, Grassi, Stefano, Donnici, Lorena, Cannalire, Rolando, Stefanelli, Irina, Ferraro, Anastasia, Esposito, Francesca, Pariani, Elena, Inverso, Donato, Montesano, Camilla, Delbue, Serena, Perlman, Stanley, Tramontano, Enzo, De Francesco, Raffaele, Summa, Vincenzo, Guidotti, Luca G, Iannacone, Matteo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165354/
https://www.ncbi.nlm.nih.gov/pubmed/36946379
http://dx.doi.org/10.15252/emmm.202317580
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author Fumagalli, Valeria
Di Lucia, Pietro
Ravà, Micol
Marotta, Davide
Bono, Elisa
Grassi, Stefano
Donnici, Lorena
Cannalire, Rolando
Stefanelli, Irina
Ferraro, Anastasia
Esposito, Francesca
Pariani, Elena
Inverso, Donato
Montesano, Camilla
Delbue, Serena
Perlman, Stanley
Tramontano, Enzo
De Francesco, Raffaele
Summa, Vincenzo
Guidotti, Luca G
Iannacone, Matteo
author_facet Fumagalli, Valeria
Di Lucia, Pietro
Ravà, Micol
Marotta, Davide
Bono, Elisa
Grassi, Stefano
Donnici, Lorena
Cannalire, Rolando
Stefanelli, Irina
Ferraro, Anastasia
Esposito, Francesca
Pariani, Elena
Inverso, Donato
Montesano, Camilla
Delbue, Serena
Perlman, Stanley
Tramontano, Enzo
De Francesco, Raffaele
Summa, Vincenzo
Guidotti, Luca G
Iannacone, Matteo
author_sort Fumagalli, Valeria
collection PubMed
description Alongside vaccines, antiviral drugs are becoming an integral part of our response to the SARS‐CoV‐2 pandemic. Nirmatrelvir—an orally available inhibitor of the 3‐chymotrypsin‐like cysteine protease—has been shown to reduce the risk of progression to severe COVID‐19. However, the impact of nirmatrelvir treatment on the development of SARS‐CoV‐2‐specific adaptive immune responses is unknown. Here, by using mouse models of SARS‐CoV‐2 infection, we show that nirmatrelvir administration blunts the development of SARS‐CoV‐2‐specific antibody and T cell responses. Accordingly, upon secondary challenge, nirmatrelvir‐treated mice recruited significantly fewer memory T and B cells to the infected lungs and mediastinal lymph nodes, respectively. Together, the data highlight a potential negative impact of nirmatrelvir treatment with important implications for clinical management and might help explain the virological and/or symptomatic relapse after treatment completion reported in some individuals.
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spelling pubmed-101653542023-05-09 Nirmatrelvir treatment of SARS‐CoV‐2‐infected mice blunts antiviral adaptive immune responses Fumagalli, Valeria Di Lucia, Pietro Ravà, Micol Marotta, Davide Bono, Elisa Grassi, Stefano Donnici, Lorena Cannalire, Rolando Stefanelli, Irina Ferraro, Anastasia Esposito, Francesca Pariani, Elena Inverso, Donato Montesano, Camilla Delbue, Serena Perlman, Stanley Tramontano, Enzo De Francesco, Raffaele Summa, Vincenzo Guidotti, Luca G Iannacone, Matteo EMBO Mol Med Reports Alongside vaccines, antiviral drugs are becoming an integral part of our response to the SARS‐CoV‐2 pandemic. Nirmatrelvir—an orally available inhibitor of the 3‐chymotrypsin‐like cysteine protease—has been shown to reduce the risk of progression to severe COVID‐19. However, the impact of nirmatrelvir treatment on the development of SARS‐CoV‐2‐specific adaptive immune responses is unknown. Here, by using mouse models of SARS‐CoV‐2 infection, we show that nirmatrelvir administration blunts the development of SARS‐CoV‐2‐specific antibody and T cell responses. Accordingly, upon secondary challenge, nirmatrelvir‐treated mice recruited significantly fewer memory T and B cells to the infected lungs and mediastinal lymph nodes, respectively. Together, the data highlight a potential negative impact of nirmatrelvir treatment with important implications for clinical management and might help explain the virological and/or symptomatic relapse after treatment completion reported in some individuals. John Wiley and Sons Inc. 2023-03-22 /pmc/articles/PMC10165354/ /pubmed/36946379 http://dx.doi.org/10.15252/emmm.202317580 Text en © 2023 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reports
Fumagalli, Valeria
Di Lucia, Pietro
Ravà, Micol
Marotta, Davide
Bono, Elisa
Grassi, Stefano
Donnici, Lorena
Cannalire, Rolando
Stefanelli, Irina
Ferraro, Anastasia
Esposito, Francesca
Pariani, Elena
Inverso, Donato
Montesano, Camilla
Delbue, Serena
Perlman, Stanley
Tramontano, Enzo
De Francesco, Raffaele
Summa, Vincenzo
Guidotti, Luca G
Iannacone, Matteo
Nirmatrelvir treatment of SARS‐CoV‐2‐infected mice blunts antiviral adaptive immune responses
title Nirmatrelvir treatment of SARS‐CoV‐2‐infected mice blunts antiviral adaptive immune responses
title_full Nirmatrelvir treatment of SARS‐CoV‐2‐infected mice blunts antiviral adaptive immune responses
title_fullStr Nirmatrelvir treatment of SARS‐CoV‐2‐infected mice blunts antiviral adaptive immune responses
title_full_unstemmed Nirmatrelvir treatment of SARS‐CoV‐2‐infected mice blunts antiviral adaptive immune responses
title_short Nirmatrelvir treatment of SARS‐CoV‐2‐infected mice blunts antiviral adaptive immune responses
title_sort nirmatrelvir treatment of sars‐cov‐2‐infected mice blunts antiviral adaptive immune responses
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165354/
https://www.ncbi.nlm.nih.gov/pubmed/36946379
http://dx.doi.org/10.15252/emmm.202317580
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