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The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies.
Manry, Jeremy; Bastard, Paul; Gervais, Adrian; Le Voyer, Tom; Rosain, Jérémie; Philippot, Quentin; Michailidis, Eleftherios; Hoffmann, Hans-Heinrich; Eto, Shohei; Garcia-Prat, Marina; Bizien, Lucy; Parra-Martínez, Alba; Yang, Rui; Haljasmägi, Liis; Migaud, Mélanie; Särekannu, Karita; Maslovskaja, Julia; de Prost, Nicolas; Tandjaoui-Lambiotte, Yacine; Luyt, Charles-Edouard; Amador-Borrero, Blanca; Gaudet, Alexandre; Poissy, Julien; Morel, Pascal; Richard, Pascale; Cognasse, Fabrice; Troya, Jesus; Trouillet-Assant, Sophie; Belot, Alexandre; Saker, Kahina; Garçon, Pierre; Rivière, Jacques G; Lagier, Jean-Christophe; Gentile, Stéphanie; Rosen, Lindsey; Shaw, Elana; Morio, Tomohiro; Tanaka, Junko; Dalmau, David; Tharaux, Pierre-Louis; Sene, Damien; Stepanian, Alain; Mégarbane, Bruno; Triantafyllia, Vasiliki; Fekkar, Arnaud; Heath, James; Franco, Jose; Anaya, Juan-Manuel; Solé-Violán, Jordi; Imberti, Luisa.
  • Manry J; INSERM U1163.
  • Bastard P; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163.
  • Gervais A; INSERM U1163.
  • Le Voyer T; INSERM U1163.
  • Rosain J; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM.
  • Philippot Q; INSERM U1163.
  • Michailidis E; The Rockefeller University, Laboratory of Virology and Infectious Disease.
  • Hoffmann HH; Laboratory of Virology and Infectious Disease, Rockefeller University.
  • Eto S; Department of Pediatrics, Graduate School of Biomedical and Health Sciences, Hiroshima University.
  • Garcia-Prat M; Pediatric Infectious Diseases and Immunodeficiencies Unit, Hospital Universitari Vall d'Hebron, Vall d'Hebron Research Institute.
  • Bizien L; INSERM U1163.
  • Parra-Martínez A; Pediatric Infectious Diseases and Immunodeficiencies Unit, Hospital Universitari Vall d'Hebron, Vall d'Hebron Research Institute.
  • Yang R; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University.
  • Haljasmägi L; University of Tartu.
  • Migaud M; INSERM U1163.
  • Särekannu K; Institute of Biomedicine and Translational Medicine, University of Tartu.
  • Maslovskaja J; Institute of Biomedicine and Translational Medicine, University of Tartu.
  • de Prost N; Hôpitaux Universitaires Henri Mondor.
  • Tandjaoui-Lambiotte Y; Avicenne Hospital, AP-HP, Bobigny, INSERM U1272, Hypoxia and Lung.
  • Luyt CE; Hôpital Pitié-Salpêtrière, Service de Médecine Intensive Réanimation, Institut de Cardiologie.
  • Amador-Borrero B; Internal Medicine Department, Lariboisière Hospital AP-HP, Paris University.
  • Gaudet A; University of Lille, U1019-UMR9017, Center for Infection and Immunity of Lille.
  • Poissy J; University of Lille, U1019-UMR9017, Center for Infection and Immunity of Lille.
  • Morel P; Etablissement Français Du Sang.
  • Richard P; Etablissement Français Du Sang.
  • Cognasse F; Etablissement Français du Sang, Auvergne-Rhône-Alpes.
  • Troya J; Department of Internal Medicine, Infanta Leonor University Hospital.
  • Trouillet-Assant S; Hospices Civils de Lyon.
  • Belot A; Hospices Civils de Lyon.
  • Saker K; Hospices Civils de Lyon.
  • Garçon P; Intensive Care Unit, Grand Hôpital de l'Est Francilien Site de Marne-La-Vallée.
  • Rivière JG; Hospital Universitari Vall d'Hebron.
  • Lagier JC; Méditerranée Infection Foundation.
  • Gentile S; Service d'Evaluation Médicale, Hôpitaux Universitaires de Marseille APHM.
  • Rosen L; National Institutes of Health.
  • Shaw E; Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health.
  • Morio T; Tokyo Medical and Dental University.
  • Tanaka J; Department of Epidemiology, Infectious Disease Control and Prevention, Graduate School of Biomedical and Health Sciences, Hiroshima Universit.
  • Dalmau D; Hospital Universitari MútuaTerrassa; Fundació Docència i Recerca MutuaTerrassa, Terrasa; Universitat de Barcelona.
  • Tharaux PL; Institut National de la Santé et de la Recherche Médicale (INSERM).
  • Sene D; Internal Medicine Department, Lariboisière Hospital AP-HP, Paris University.
  • Stepanian A; Service d'Hématologie Biologique, Hôpital Lariboisière, AP-HP and EA3518, Institut Universitaire d'Hématologie-Hôpital Saint Louis, Université Paris.
  • Mégarbane B; Réanimation Médicale et Toxicologique, Hôpital Lariboisière (AP-HP), Université Paris-Diderot, INSERM Unité Mixte de Recherche Scientifique (UMRS) 1144.
  • Triantafyllia V; Laboratory of Immunobiology, Center for Clinical, Experimental Surgery, and Translational Research, Biomedical Research Foundation of the Academy of Athens.
  • Fekkar A; INSERM U1163.
  • Heath J; Institute for Systems Biology.
  • Franco J; University of Antioquia.
  • Anaya JM; Universidad del Rosario.
  • Solé-Violán J; Intensive Care Medicine, University Hospital of Gran Canaria Dr. Negrín, Canarian Health System.
  • Imberti L; CREA Laboratory (AIL Center for Hemato-Oncologic Research), Diagnostic Department, ASST Spedali Civili di Brescia.
Res Sq ; 2022 Jan 14.
Article in English | MEDLINE | ID: covidwho-1766249
ABSTRACT
SARS-CoV-2 infection fatality rate (IFR) doubles with every five years of age from childhood onward. Circulating autoantibodies neutralizing IFN-α, IFN-ω, and/or IFN-ß are found in ~20% of deceased patients across age groups. In the general population, they are found in ~1% of individuals aged 20-70 years and in >4% of those >70 years old. With a sample of 1,261 deceased patients and 34,159 uninfected individuals, we estimated both IFR and relative risk of death (RRD) across age groups for individuals carrying autoantibodies neutralizing type I IFNs, relative to non-carriers. For autoantibodies neutralizing IFN-α2 or IFN-ω, the RRD was 17.0[95% CI11.7-24.7] for individuals under 70 years old and 5.8[4.5-7.4] for individuals aged 70 and over, whereas, for autoantibodies neutralizing both molecules, the RRD was 188.3[44.8-774.4] and 7.2[5.0-10.3], respectively. IFRs increased with age, from 0.17%[0.12-0.31] for individuals <40 years old to 26.7%[20.3-35.2] for those ≥80 years old for autoantibodies neutralizing IFN-α2 or IFN-ω, and from 0.84%[0.31-8.28] to 40.5%[27.82-61.20] for the same two age groups, for autoantibodies neutralizing both molecules. Autoantibodies against type I IFNs increase IFRs, and are associated with high RRDs, particularly those neutralizing both IFN-α2 and -ω. Remarkably, IFR increases with age, whereas RRD decreases with age. Autoimmunity to type I IFNs appears to be second only to age among common predictors of COVID-19 death.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Language: English Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Language: English Year: 2022 Document Type: Article