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Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model

Impaired type I interferons (IFNs) production or signaling have been associated with severe COVID-19, further promoting the evaluation of recombinant type I IFNs as therapeutics against SARS-CoV-2 infection. In the Syrian hamster model, we show that intranasal administration of IFN-α starting one da...

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Autores principales: Bessière, Pierre, Wasniewski, Marine, Picard-Meyer, Evelyne, Servat, Alexandre, Figueroa, Thomas, Foret-Lucas, Charlotte, Coggon, Amelia, Lesellier, Sandrine, Boué, Frank, Cebron, Nathan, Gausserès, Blandine, Trumel, Catherine, Foucras, Gilles, Salguero, Francisco J., Monchatre-Leroy, Elodie, Volmer, Romain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376007/
https://www.ncbi.nlm.nih.gov/pubmed/34370799
http://dx.doi.org/10.1371/journal.ppat.1009427
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author Bessière, Pierre
Wasniewski, Marine
Picard-Meyer, Evelyne
Servat, Alexandre
Figueroa, Thomas
Foret-Lucas, Charlotte
Coggon, Amelia
Lesellier, Sandrine
Boué, Frank
Cebron, Nathan
Gausserès, Blandine
Trumel, Catherine
Foucras, Gilles
Salguero, Francisco J.
Monchatre-Leroy, Elodie
Volmer, Romain
author_facet Bessière, Pierre
Wasniewski, Marine
Picard-Meyer, Evelyne
Servat, Alexandre
Figueroa, Thomas
Foret-Lucas, Charlotte
Coggon, Amelia
Lesellier, Sandrine
Boué, Frank
Cebron, Nathan
Gausserès, Blandine
Trumel, Catherine
Foucras, Gilles
Salguero, Francisco J.
Monchatre-Leroy, Elodie
Volmer, Romain
author_sort Bessière, Pierre
collection PubMed
description Impaired type I interferons (IFNs) production or signaling have been associated with severe COVID-19, further promoting the evaluation of recombinant type I IFNs as therapeutics against SARS-CoV-2 infection. In the Syrian hamster model, we show that intranasal administration of IFN-α starting one day pre-infection or one day post-infection limited weight loss and decreased viral lung titers. By contrast, intranasal administration of IFN-α starting at the onset of symptoms three days post-infection had no impact on the clinical course of SARS-CoV-2 infection. Our results provide evidence that early type I IFN treatment is beneficial, while late interventions are ineffective, although not associated with signs of enhanced disease.
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spelling pubmed-83760072021-08-20 Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model Bessière, Pierre Wasniewski, Marine Picard-Meyer, Evelyne Servat, Alexandre Figueroa, Thomas Foret-Lucas, Charlotte Coggon, Amelia Lesellier, Sandrine Boué, Frank Cebron, Nathan Gausserès, Blandine Trumel, Catherine Foucras, Gilles Salguero, Francisco J. Monchatre-Leroy, Elodie Volmer, Romain PLoS Pathog Research Article Impaired type I interferons (IFNs) production or signaling have been associated with severe COVID-19, further promoting the evaluation of recombinant type I IFNs as therapeutics against SARS-CoV-2 infection. In the Syrian hamster model, we show that intranasal administration of IFN-α starting one day pre-infection or one day post-infection limited weight loss and decreased viral lung titers. By contrast, intranasal administration of IFN-α starting at the onset of symptoms three days post-infection had no impact on the clinical course of SARS-CoV-2 infection. Our results provide evidence that early type I IFN treatment is beneficial, while late interventions are ineffective, although not associated with signs of enhanced disease. Public Library of Science 2021-08-09 /pmc/articles/PMC8376007/ /pubmed/34370799 http://dx.doi.org/10.1371/journal.ppat.1009427 Text en © 2021 Bessière et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bessière, Pierre
Wasniewski, Marine
Picard-Meyer, Evelyne
Servat, Alexandre
Figueroa, Thomas
Foret-Lucas, Charlotte
Coggon, Amelia
Lesellier, Sandrine
Boué, Frank
Cebron, Nathan
Gausserès, Blandine
Trumel, Catherine
Foucras, Gilles
Salguero, Francisco J.
Monchatre-Leroy, Elodie
Volmer, Romain
Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model
title Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model
title_full Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model
title_fullStr Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model
title_full_unstemmed Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model
title_short Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model
title_sort intranasal type i interferon treatment is beneficial only when administered before clinical signs onset in the sars-cov-2 hamster model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376007/
https://www.ncbi.nlm.nih.gov/pubmed/34370799
http://dx.doi.org/10.1371/journal.ppat.1009427
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