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Auto-antibodies against type I IFNs in > 10% of critically ill COVID-19 patients: a prospective multicentre study.
Arrestier, Romain; Bastard, Paul; Belmondo, Thibaut; Voiriot, Guillaume; Urbina, Tomas; Luyt, Charles-Edouard; Gervais, Adrian; Bizien, Lucy; Segaux, Lauriane; Ben Ahmed, Mariem; Bellaïche, Raphaël; Pham, Taï; Ait-Hamou, Zakaria; Roux, Damien; Clere-Jehl, Raphael; Azoulay, Elie; Gaudry, Stéphane; Mayaux, Julien; Fage, Nicolas; Ait-Oufella, Hafid; Moncomble, Elsa; Parfait, Mélodie; Dorgham, Karim; Gorochov, Guy; Mekontso-Dessap, Armand; Canoui-Poitrine, Florence; Casanova, Jean-Laurent; Hue, Sophie; de Prost, Nicolas.
  • Arrestier R; Service de Médecine Intensive Réanimation, Service de Réanimation Médicale, Hôpital Henri Mondor, Hôpitaux Universitaires Henri Mondor, Assistance Publique-Hôpitaux de Paris, Créteil, 94010, Paris, Cedex, France.
  • Bastard P; Groupe de Recherche Clinique CARMAS, Faculté de Santé de Créteil, Université Paris Est Créteil, Créteil, 94010, Paris, Cedex, France.
  • Belmondo T; INSERM, IMRB, Université Paris Est Créteil, Créteil, 94010, Paris, Cedex, France.
  • Voiriot G; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Urbina T; Imagine Institute, University of Paris, Paris, France.
  • Luyt CE; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.
  • Gervais A; Département d'Hématologie et d'Immunologie Biologiques, Assistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalo-Universitaire Chenevier Mondor, Créteil, 94010, Paris, France.
  • Bizien L; Service de Médecine Intensive-Réanimation, Hôpital Tenon, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Segaux L; Service de Médecine Intensive-Réanimation, Hôpital Saint-Antoine, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Ben Ahmed M; Service de Médecine Intensive Réanimation, Sorbonne Université, Hôpitaux Universitaires Pitié Salpêtrière-Charles Foix, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Bellaïche R; INSERM UMRS_1166-iCAN, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Pham T; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Ait-Hamou Z; Imagine Institute, University of Paris, Paris, France.
  • Roux D; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.
  • Clere-Jehl R; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Azoulay E; Imagine Institute, University of Paris, Paris, France.
  • Gaudry S; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.
  • Mayaux J; INSERM, IMRB, Université Paris Est Créteil, Créteil, 94010, Paris, Cedex, France.
  • Fage N; Unité de Recherche Clinique AP-HP, Hôpitaux Henri-Mondor, 94010, Creteil, Cedex, France.
  • Ait-Oufella H; Imagine Institute, University of Paris, Paris, France.
  • Moncomble E; Service d'Anesthésie-Réanimation Chirurgicale, Assistance Publique-Hôpitaux de Paris, Hôpitaux Universitaires Henri Mondor, 94000, Créteil, France.
  • Parfait M; Service de Médecine Intensive-Réanimation, AP-HP, Hôpital de Bicêtre, DMU 4 CORREVE Maladies du Cœur et des Vaisseaux, FHU Sepsis, Groupe de Recherche Clinique CARMAS, Le Kremlin-Bicêtre, France.
  • Dorgham K; Service de Médecine Intensive-Réanimation, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris (AP-HP), Centre & Université de Paris, Paris, France.
  • Gorochov G; Médecine Intensive Réanimation, AP-HP, Hôpital Louis Mourier, DMU ESPRIT, 92700, Colombes, France.
  • Mekontso-Dessap A; Service de médecine intensive et réanimation, Hôpital Saint-Louis, Assistance Publique Des Hôpitaux de Paris, Paris, France.
  • Canoui-Poitrine F; Service de médecine intensive et réanimation, Hôpital Saint-Louis, Assistance Publique Des Hôpitaux de Paris, Paris, France.
  • Casanova JL; Département de réanimation médico-chirurgicale, APHP Hôpital Avicenne, Bobigny, France.
  • Hue S; Groupe Hospitalier Pitié Salpêtrière, Assistance Publique Hôpitaux de Paris, Service de Pneumologie et Réanimation Médicale, Paris, France.
  • de Prost N; Service de Médecine Intensive-Réanimation, AP-HP, Hôpital de Bicêtre, DMU 4 CORREVE Maladies du Cœur et des Vaisseaux, FHU Sepsis, Groupe de Recherche Clinique CARMAS, Le Kremlin-Bicêtre, France.
Ann Intensive Care ; 12(1): 121, 2022 Dec 31.
Article in English | MEDLINE | ID: covidwho-2196445
ABSTRACT

BACKGROUND:

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.

RESULTS:

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 neutralizing type I IFN-α2, ß and/or ω were found in 96 patients (10.3%). Demographics and comorbidities did not differ between patients with versus without auto-Abs. At ICU admission, Auto-Abs positive patients required a higher FiO2 (100% (70-100) vs. 90% (60-100), p = 0.01), but were not different in other characteristics. Mortality at day 28 was not different between patients with and without auto-Abs (18.7 vs. 23.7%, p = 0.279). In multivariable analysis, 28-day mortality was associated with age (adjusted odds ratio (aOR) = 1.06 [1.04-1.08], p < 0.001), SOFA score (aOR = 1.18 [1.12-1.23], p < 0.001) and immunosuppression (aOR = 1.82 [1.1-3.0], p = 0.02), but not with the presence of auto-Abs (aOR = 0.69 [0.38-1.26], p = 0.23).

CONCLUSIONS:

In ICU patients, auto-Abs against type I IFNs were found in at least 10% of patients with critical COVID-19 pneumonia. They were not associated with day 28 mortality.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Language: English Journal: Ann Intensive Care Year: 2022 Document Type: Article Affiliation country: S13613-022-01095-5

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Language: English Journal: Ann Intensive Care Year: 2022 Document Type: Article Affiliation country: S13613-022-01095-5