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Autoantibodies Neutralizing Type I Interferons in 20% of COVID-19 Deaths in a French Hospital
Recent studies reported the presence of pre-existing autoantibodies (auto-Abs) neutralizing type I interferons (IFNs) in at least 15% of patients with critical COVID-19 pneumonia. In one study, these auto-Abs were found in almost 20% of deceased patients across all ages. We aimed to assess the preva...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791677/ https://www.ncbi.nlm.nih.gov/pubmed/35083626 http://dx.doi.org/10.1007/s10875-021-01203-3 |
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author | Chauvineau-Grenier, Angélique Bastard, Paul Servajean, Antoine Gervais, Adrian Rosain, Jérémie Jouanguy, Emmanuelle Cobat, Aurélie Casanova, Jean-Laurent Rossi, Benjamin |
author_facet | Chauvineau-Grenier, Angélique Bastard, Paul Servajean, Antoine Gervais, Adrian Rosain, Jérémie Jouanguy, Emmanuelle Cobat, Aurélie Casanova, Jean-Laurent Rossi, Benjamin |
author_sort | Chauvineau-Grenier, Angélique |
collection | PubMed |
description | Recent studies reported the presence of pre-existing autoantibodies (auto-Abs) neutralizing type I interferons (IFNs) in at least 15% of patients with critical COVID-19 pneumonia. In one study, these auto-Abs were found in almost 20% of deceased patients across all ages. We aimed to assess the prevalence and clinical impact of the auto-Abs to type I IFNs in the Seine-Saint-Denis district, which was one of the most affected areas by COVID-19 in France during the first wave. We tested for the presence of auto-Abs neutralizing type I IFNs in a cohort of patients admitted for critical COVID-19 pneumonia during the first wave in the spring of 2020 in the medicine departments at Robert Ballanger Hospital, Aulnay sous Bois. We found circulating auto-Abs that neutralized 100 pg/mL IFN-α2 and/or IFN-ω in the plasma (diluted 1/10) of 7.9% (11 of 139) of the patients hospitalized for critical COVID-19. The presence of neutralizing auto-Abs was associated with an increased risk of mortality, as these auto-Abs were detected in 21% of patients who died from COVID-19 pneumonia. Deceased patients with and without auto-Abs did not present overt clinical differences. These results confirm both the importance of type I IFN immunity in host defense against SARS-CoV-2 infection and the usefulness of detection of auto-Abs neutralizing type I IFNs in the management of patients. |
format | Online Article Text |
id | pubmed-8791677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-87916772022-01-27 Autoantibodies Neutralizing Type I Interferons in 20% of COVID-19 Deaths in a French Hospital Chauvineau-Grenier, Angélique Bastard, Paul Servajean, Antoine Gervais, Adrian Rosain, Jérémie Jouanguy, Emmanuelle Cobat, Aurélie Casanova, Jean-Laurent Rossi, Benjamin J Clin Immunol Original Article Recent studies reported the presence of pre-existing autoantibodies (auto-Abs) neutralizing type I interferons (IFNs) in at least 15% of patients with critical COVID-19 pneumonia. In one study, these auto-Abs were found in almost 20% of deceased patients across all ages. We aimed to assess the prevalence and clinical impact of the auto-Abs to type I IFNs in the Seine-Saint-Denis district, which was one of the most affected areas by COVID-19 in France during the first wave. We tested for the presence of auto-Abs neutralizing type I IFNs in a cohort of patients admitted for critical COVID-19 pneumonia during the first wave in the spring of 2020 in the medicine departments at Robert Ballanger Hospital, Aulnay sous Bois. We found circulating auto-Abs that neutralized 100 pg/mL IFN-α2 and/or IFN-ω in the plasma (diluted 1/10) of 7.9% (11 of 139) of the patients hospitalized for critical COVID-19. The presence of neutralizing auto-Abs was associated with an increased risk of mortality, as these auto-Abs were detected in 21% of patients who died from COVID-19 pneumonia. Deceased patients with and without auto-Abs did not present overt clinical differences. These results confirm both the importance of type I IFN immunity in host defense against SARS-CoV-2 infection and the usefulness of detection of auto-Abs neutralizing type I IFNs in the management of patients. Springer US 2022-01-27 2022 /pmc/articles/PMC8791677/ /pubmed/35083626 http://dx.doi.org/10.1007/s10875-021-01203-3 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Chauvineau-Grenier, Angélique Bastard, Paul Servajean, Antoine Gervais, Adrian Rosain, Jérémie Jouanguy, Emmanuelle Cobat, Aurélie Casanova, Jean-Laurent Rossi, Benjamin Autoantibodies Neutralizing Type I Interferons in 20% of COVID-19 Deaths in a French Hospital |
title | Autoantibodies Neutralizing Type I Interferons in 20% of COVID-19 Deaths in a French Hospital |
title_full | Autoantibodies Neutralizing Type I Interferons in 20% of COVID-19 Deaths in a French Hospital |
title_fullStr | Autoantibodies Neutralizing Type I Interferons in 20% of COVID-19 Deaths in a French Hospital |
title_full_unstemmed | Autoantibodies Neutralizing Type I Interferons in 20% of COVID-19 Deaths in a French Hospital |
title_short | Autoantibodies Neutralizing Type I Interferons in 20% of COVID-19 Deaths in a French Hospital |
title_sort | autoantibodies neutralizing type i interferons in 20% of covid-19 deaths in a french hospital |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791677/ https://www.ncbi.nlm.nih.gov/pubmed/35083626 http://dx.doi.org/10.1007/s10875-021-01203-3 |
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