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Autoantibodies Neutralizing Type III Interferons Are Uncommon in Patients with Severe Coronavirus Disease 2019 Pneumonia.
Vanker, Martti; Särekannu, Karita; Fekkar, Arnaud; Jørgensen, Sofie Eg; Haljasmägi, Liis; Kallaste, Anne; Kisand, Kalle; Lember, Margus; Peterson, Pärt; Menon, Madhvi; Hussell, Tracy; Knight, Sean; Moore-Stanley, James; Bastard, Paul; Zhang, Shen-Ying; Mogensen, Trine H; Philippot, Quentin; Zhang, Qian; Puel, Anne; Casanova, Jean-Laurent; Kisand, Kai.
Afiliação
  • Vanker M; Institute of Biomedicine and Translational Medicine; Institute of Clinical Medicine; University of Tartu, Tartu, Estonia.
  • Särekannu K; Institute of Biomedicine and Translational Medicine; Institute of Clinical Medicine; University of Tartu, Tartu, Estonia.
  • Fekkar A; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Jørgensen SE; Service de Parasitologie-Mycologie, Groupe Hospitalier Pitié Salpêtrière, AP-HP, Paris, France.
  • Haljasmägi L; Department of Infectious Diseases, Aarhus University Hospital, Aarhus N, Denmark.
  • Kallaste A; Department of Biomedicine, Aarhus University, Aarhus C, Denmark.
  • Kisand K; Institute of Biomedicine and Translational Medicine; Institute of Clinical Medicine; University of Tartu, Tartu, Estonia.
  • Lember M; Department of Internal Medicine, Tartu University Hospital, Tartu, Estonia.
  • Peterson P; Department of Internal Medicine, Institute of Clinical Medicine; University of Tartu, Tartu, Estonia.
  • Menon M; Department of Internal Medicine, Tartu University Hospital, Tartu, Estonia.
  • Hussell T; Department of Internal Medicine, Institute of Clinical Medicine; University of Tartu, Tartu, Estonia.
  • Knight S; Institute of Biomedicine and Translational Medicine; Institute of Clinical Medicine; University of Tartu, Tartu, Estonia.
  • Moore-Stanley J; Lydia Becker Institute of Immunology and Inflammation, Division of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom.
  • Bastard P; Lydia Becker Institute of Immunology and Inflammation, Division of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom.
  • Zhang SY; Lydia Becker Institute of Immunology and Inflammation, Division of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom.
  • Mogensen TH; Respiratory Department, Salford Care Organisation, Northern Care Alliance Foundation Trust, Manchester, United Kingdom.
  • Philippot Q; Lydia Becker Institute of Immunology and Inflammation, Division of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom.
  • Zhang Q; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Puel A; University of Paris, Imagine Institute, Paris, France.
  • Casanova JL; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, New York, USA.
  • Kisand K; Department of Pediatrics, Necker Hospital for Sick Children, AP-HP, Paris, France.
J Interferon Cytokine Res ; 43(9): 379-393, 2023 09.
Article em En | MEDLINE | ID: mdl-37253131
ABSTRACT
Autoantibodies (AABs) neutralizing type I interferons (IFN) underlie about 15% of cases of critical coronavirus disease 2019 (COVID-19) pneumonia. The impact of autoimmunity toward type III IFNs remains unexplored. We included samples from 1,002 patients with COVID-19 (50% with severe disease) and 1,489 SARS-CoV-2-naive individuals. We studied the prevalence and neutralizing capacity of AABs toward IFNλ and IFNα. Luciferase-based immunoprecipitation method was applied using pooled IFNα (subtypes 1, 2, 8, and 21) or pooled IFNλ1-IFNλ3 as antigens, followed by reporter cell-based neutralization assay. In the SARS-CoV-2-naive cohort, IFNλ AABs were more common (8.5%) than those targeting IFNα2 (2.9%) and were related with older age. In the COVID-19 cohort the presence of autoreactivity to IFNλ did not associate with severe disease [odds ratio (OR) 0.84; 95% confidence interval (CI) 0.40-1.73], unlike to IFNα (OR 4.88; 95% CI 2.40-11.06; P < 0.001). Most IFNλ AAB-positive COVID-19 samples (67%) did not neutralize any of the 3 IFNλ subtypes. Pan-IFNλ neutralization occurred in 5 patients (0.50%), who all suffered from severe COVID-19 pneumonia, and 4 of them neutralized IFNα2 in addition to IFNλ. Overall, AABs to type III IFNs are rarely neutralizing, and do not seem to predispose to severe COVID-19 pneumonia on their own.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Interferon Tipo I / COVID-19 Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Interferon Tipo I / COVID-19 Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article