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No increased prevalence of autoantibodies neutralizing type I IFNs in idiopathic pulmonary fibrosis patients
SARS-CoV2 infection has a poor prognosis in patients affected of idiopathic pulmonary fibrosis (IPF). Autoantibodies (auto-Abs) neutralizing type I interferons (IFNs) are found in the blood of at least 15% of patients with life-threatening COVID-19 pneumonia. Because of the elevated prevalence of so...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025783/ https://www.ncbi.nlm.nih.gov/pubmed/36941652 http://dx.doi.org/10.1186/s12931-023-02396-4 |
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author | Philippot, Quentin Bastard, Paul Puel, Anne Casanova, Jean-Laurent Cobat, Aurélie Laouénan, Cédric Tardivon, Coralie Crestani, Bruno Borie, Raphael |
author_facet | Philippot, Quentin Bastard, Paul Puel, Anne Casanova, Jean-Laurent Cobat, Aurélie Laouénan, Cédric Tardivon, Coralie Crestani, Bruno Borie, Raphael |
author_sort | Philippot, Quentin |
collection | PubMed |
description | SARS-CoV2 infection has a poor prognosis in patients affected of idiopathic pulmonary fibrosis (IPF). Autoantibodies (auto-Abs) neutralizing type I interferons (IFNs) are found in the blood of at least 15% of patients with life-threatening COVID-19 pneumonia. Because of the elevated prevalence of some auto-Abs in IPF patients, we hypothesize that the prevalence of auto-Abs neutralizing type I IFNs might be increased in the IPF population and then explained specific poor outcome after COVID-19. We screened the plasma of 247 consecutive IPF patients for the presence of auto-Abs neutralizing type I IFNs. Three patients displayed auto-Abs neutralizing type I IFNs. Among them, the only patient with documented SARS-CoV-2 infection experienced life threatening COVID-19 pneumonia. The prevalence of auto-Abs neutralizing type I IFNs in this cohort of IPF patients was not significantly different from the one of the general population. Overall, this study did not suggest any association between auto-Abs neutralizing type I IFNs and IPF. |
format | Online Article Text |
id | pubmed-10025783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100257832023-03-21 No increased prevalence of autoantibodies neutralizing type I IFNs in idiopathic pulmonary fibrosis patients Philippot, Quentin Bastard, Paul Puel, Anne Casanova, Jean-Laurent Cobat, Aurélie Laouénan, Cédric Tardivon, Coralie Crestani, Bruno Borie, Raphael Respir Res Correspondence SARS-CoV2 infection has a poor prognosis in patients affected of idiopathic pulmonary fibrosis (IPF). Autoantibodies (auto-Abs) neutralizing type I interferons (IFNs) are found in the blood of at least 15% of patients with life-threatening COVID-19 pneumonia. Because of the elevated prevalence of some auto-Abs in IPF patients, we hypothesize that the prevalence of auto-Abs neutralizing type I IFNs might be increased in the IPF population and then explained specific poor outcome after COVID-19. We screened the plasma of 247 consecutive IPF patients for the presence of auto-Abs neutralizing type I IFNs. Three patients displayed auto-Abs neutralizing type I IFNs. Among them, the only patient with documented SARS-CoV-2 infection experienced life threatening COVID-19 pneumonia. The prevalence of auto-Abs neutralizing type I IFNs in this cohort of IPF patients was not significantly different from the one of the general population. Overall, this study did not suggest any association between auto-Abs neutralizing type I IFNs and IPF. BioMed Central 2023-03-20 2023 /pmc/articles/PMC10025783/ /pubmed/36941652 http://dx.doi.org/10.1186/s12931-023-02396-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Correspondence Philippot, Quentin Bastard, Paul Puel, Anne Casanova, Jean-Laurent Cobat, Aurélie Laouénan, Cédric Tardivon, Coralie Crestani, Bruno Borie, Raphael No increased prevalence of autoantibodies neutralizing type I IFNs in idiopathic pulmonary fibrosis patients |
title | No increased prevalence of autoantibodies neutralizing type I IFNs in idiopathic pulmonary fibrosis patients |
title_full | No increased prevalence of autoantibodies neutralizing type I IFNs in idiopathic pulmonary fibrosis patients |
title_fullStr | No increased prevalence of autoantibodies neutralizing type I IFNs in idiopathic pulmonary fibrosis patients |
title_full_unstemmed | No increased prevalence of autoantibodies neutralizing type I IFNs in idiopathic pulmonary fibrosis patients |
title_short | No increased prevalence of autoantibodies neutralizing type I IFNs in idiopathic pulmonary fibrosis patients |
title_sort | no increased prevalence of autoantibodies neutralizing type i ifns in idiopathic pulmonary fibrosis patients |
topic | Correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025783/ https://www.ncbi.nlm.nih.gov/pubmed/36941652 http://dx.doi.org/10.1186/s12931-023-02396-4 |
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