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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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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. |
format | Online Article Text |
id | pubmed-8376007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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