<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Arrestier R</submitter><funding>NCRR NIH HHS</funding><funding>NIAID NIH HHS</funding><pagination>121</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9803887</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Auto-antibodies (auto-Abs) neutralizing type I interferons (IFN) have been found in about 15% of critical cases COVID-19 pneumonia and less than 1% of mild or asymptomatic cases. Determining whether auto-Abs influence presentation and outcome of critically ill COVID-19 patients could lead to specific therapeutic interventions. Our objectives were to compare the severity at admission and the mortality of patients hospitalized for critical COVID-19 in ICU with versus without auto-Abs.&lt;h4>Results&lt;/h4>We conducted a prospective multicentre cohort study including patients admitted in 11 intensive care units (ICUs) from Great Paris area hospitals with proven SARS-CoV-2 infection and acute respiratory failure. 925 critically ill COVID-19 patients were included. Auto-Abs neutral</pubmed_abstract><journal>Annals of intensive care</journal><pubmed_title>Auto-antibodies against type I IFNs in > 10% of critically ill COVID-19 patients: a prospective multicentre study.</pubmed_title><pmcid>PMC9803887</pmcid><funding_grant_id>R01 AI088364</funding_grant_id><funding_grant_id>R01 AI163029</funding_grant_id><funding_grant_id>UL1 RR024143</funding_grant_id><pubmed_authors>Moncomble E</pubmed_authors><pubmed_authors>Ben Ahmed M</pubmed_authors><pubmed_authors>Parfait M</pubmed_authors><pubmed_authors>Bizien L</pubmed_authors><pubmed_authors>Gaudry S</pubmed_authors><pubmed_authors>Mekontso-Dessap A</pubmed_authors><pubmed_authors>Pham T</pubmed_authors><pubmed_authors>Gervais A</pubmed_authors><pubmed_authors>Fage N</pubmed_authors><pubmed_authors>Belmondo T</pubmed_authors><pubmed_authors>Dorgham K</pubmed_authors><pubmed_authors>de Prost N</pubmed_authors><pubmed_authors>Luyt CE</pubmed_authors><pubmed_authors>Azoulay E</pubmed_authors><pubmed_authors>Voiriot G</pubmed_authors><pubmed_authors>Bastard P</pubmed_authors><pubmed_authors>Roux D</pubmed_authors><pubmed_authors>Hue S</pubmed_authors><pubmed_authors>Arrestier R</pubmed_authors><pubmed_authors>Urbina T</pubmed_authors><pubmed_authors>Casanova JL</pubmed_authors><pubmed_authors>Clere-Jehl R</pubmed_authors><pubmed_authors>Ait-Oufella H</pubmed_authors><pubmed_authors>Ait-Hamou Z</pubmed_authors><pubmed_authors>Mayaux J</pubmed_authors><pubmed_authors>Canoui-Poitrine F</pubmed_authors><pubmed_authors>Gorochov G</pubmed_authors><pubmed_authors>Segaux L</pubmed_authors><pubmed_authors>Bellaiche R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Auto-antibodies against type I IFNs in > 10% of critically ill COVID-19 patients: a prospective multicentre study.</name><description>&lt;h4>Background&lt;/h4>Auto-antibodies (auto-Abs) neutralizing type I interferons (IFN) have been found in about 15% of critical cases COVID-19 pneumonia and less than 1% of mild or asymptomatic cases. Determining whether auto-Abs influence presentation and outcome of critically ill COVID-19 patients could lead to specific therapeutic interventions. Our objectives were to compare the severity at admission and the mortality of patients hospitalized for critical COVID-19 in ICU with versus without auto-Abs.&lt;h4>Results&lt;/h4>We conducted a prospective multicentre cohort study including patients admitted in 11 intensive care units (ICUs) from Great Paris area hospitals with proven SARS-CoV-2 infection and acute respiratory failure. 925 critically ill COVID-19 patients were included. Auto-Abs neutral</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-07-14T16:59:02.331Z</modification><creation>2025-04-20T00:13:12.626Z</creation></dates><accession>S-EPMC9803887</accession><cross_references><pubmed>36586050</pubmed><doi>10.1186/s13613-022-01095-5</doi></cross_references></HashMap>