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...
Main Authors: | , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2021-08-01
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Series: | PLoS Pathogens |
Online Access: | https://doi.org/10.1371/journal.ppat.1009427 |
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author | Pierre Bessière Marine Wasniewski Evelyne Picard-Meyer Alexandre Servat Thomas Figueroa Charlotte Foret-Lucas Amelia Coggon Sandrine Lesellier Frank Boué Nathan Cebron Blandine Gausserès Catherine Trumel Gilles Foucras Francisco J Salguero Elodie Monchatre-Leroy Romain Volmer |
author_facet | Pierre Bessière Marine Wasniewski Evelyne Picard-Meyer Alexandre Servat Thomas Figueroa Charlotte Foret-Lucas Amelia Coggon Sandrine Lesellier Frank Boué Nathan Cebron Blandine Gausserès Catherine Trumel Gilles Foucras Francisco J Salguero Elodie Monchatre-Leroy Romain Volmer |
author_sort | Pierre Bessière |
collection | DOAJ |
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. |
first_indexed | 2024-04-10T17:48:20Z |
format | Article |
id | doaj.art-1d0652f69d9a41f9a08e502c8b431fb7 |
institution | Directory Open Access Journal |
issn | 1553-7366 1553-7374 |
language | English |
last_indexed | 2024-04-10T17:48:20Z |
publishDate | 2021-08-01 |
publisher | Public Library of Science (PLoS) |
record_format | Article |
series | PLoS Pathogens |
spelling | doaj.art-1d0652f69d9a41f9a08e502c8b431fb72023-02-02T22:56:58ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742021-08-01178e100942710.1371/journal.ppat.1009427Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model.Pierre BessièreMarine WasniewskiEvelyne Picard-MeyerAlexandre ServatThomas FigueroaCharlotte Foret-LucasAmelia CoggonSandrine LesellierFrank BouéNathan CebronBlandine GausserèsCatherine TrumelGilles FoucrasFrancisco J SalgueroElodie Monchatre-LeroyRomain VolmerImpaired 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.https://doi.org/10.1371/journal.ppat.1009427 |
spellingShingle | Pierre Bessière Marine Wasniewski Evelyne Picard-Meyer Alexandre Servat Thomas Figueroa Charlotte Foret-Lucas Amelia Coggon Sandrine Lesellier Frank Boué Nathan Cebron Blandine Gausserès Catherine Trumel Gilles Foucras Francisco J Salguero Elodie Monchatre-Leroy Romain Volmer Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model. PLoS Pathogens |
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 |
url | https://doi.org/10.1371/journal.ppat.1009427 |
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