Interindividual clinical variability in the course of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is vast. We report that at least 101 of 987 patients with life-threatening coronavirus disease 2019 (COVID-19) pneumonia had neutralizing immunoglobulin G (IgG) autoantibodies (auto-Abs) against interferon-omega (IFN-omega) (13 patients), against the 13 types of IFN-alpha (36), or against both (52) at the onset of critical disease; a few also had auto-Abs against the other three type I IFNs. The auto-Abs neutralize the ability of the corresponding type I IFNs to block SARS-CoV-2 infection in vitro. These auto-Abs were not found in 663 individuals with asymptomatic or mild SARS-CoV-2 infection and were present in only 4 of 1227 healthy individuals. Patients with auto-Abs were aged 25 to 87 years and 95 of the 101 were men. A B cell autoimmune phenocopy of inborn errors of type I IFN immunity accounts for lifethreatening COVID-19 pneumonia in at least 2.6% of women and 12.5% of men.

Bastard, P., Rosen, L.b., Zhang, Q., Michailidis, E., Hoffmann, H., Zhang, Y., et al. (2020). Autoantibodies against type I IFNs in patients with life-threatening COVID-19. SCIENCE, 370(6515), 423-+ [10.1126/science.abd4585].

Autoantibodies against type I IFNs in patients with life-threatening COVID-19

Aiuti, Alessandro;Biondi, Andrea;
2020-01-01

Abstract

Interindividual clinical variability in the course of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is vast. We report that at least 101 of 987 patients with life-threatening coronavirus disease 2019 (COVID-19) pneumonia had neutralizing immunoglobulin G (IgG) autoantibodies (auto-Abs) against interferon-omega (IFN-omega) (13 patients), against the 13 types of IFN-alpha (36), or against both (52) at the onset of critical disease; a few also had auto-Abs against the other three type I IFNs. The auto-Abs neutralize the ability of the corresponding type I IFNs to block SARS-CoV-2 infection in vitro. These auto-Abs were not found in 663 individuals with asymptomatic or mild SARS-CoV-2 infection and were present in only 4 of 1227 healthy individuals. Patients with auto-Abs were aged 25 to 87 years and 95 of the 101 were men. A B cell autoimmune phenocopy of inborn errors of type I IFN immunity accounts for lifethreatening COVID-19 pneumonia in at least 2.6% of women and 12.5% of men.
2020
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/03 - GENETICA MEDICA
English
Con Impact Factor ISI
Adult
Aged
Aged, 80 and over
Antibodies, Neutralizing
Asymptomatic Infections
Autoantibodies
Betacoronavirus
COVID-19
Case-Control Studies
Coronavirus Infections
Critical Illness
Female
Humans
Immunoglobulin G
Interferon Type I
Interferon alpha-2
Male
Middle Aged
Pandemics
Pneumonia, Viral
SARS-CoV-2
Bastard, P., Rosen, L.b., Zhang, Q., Michailidis, E., Hoffmann, H., Zhang, Y., et al. (2020). Autoantibodies against type I IFNs in patients with life-threatening COVID-19. SCIENCE, 370(6515), 423-+ [10.1126/science.abd4585].
Bastard, P; Rosen, Lb; Zhang, Q; Michailidis, E; Hoffmann, H; Zhang, Y; Dorgham, K; Philippot, Q; Rosain, J; Béziat, V; Manry, J; Shaw, E; Haljasmägi, L; Peterson, P; Lorenzo, L; Bizien, L; Trouillet-Assant, S; Dobbs, K; de Jesus, Aa; Belot, A; Kallaste, A; Catherinot, E; Tandjaoui-Lambiotte, Y; Le Pen, J; Kerner, G; Bigio, B; Seeleuthner, Y; Yang, R; Bolze, A; Spaan, An; Delmonte, Om; Abers, Ms; Aiuti, A; Casari, G; Lampasona, V; Piemonti, L; Ciceri, F; Bilguvar, K; Lifton, Rp; Vasse, M; Smadja, Dm; Migaud, M; Hadjadj, J; Terrier, B; Duffy, D; Quintana-Murci, L; van de Beek, D; Roussel, L; Vinh, Dc; Tangye, Sg; Haerynck, F; Dalmau, D; Martinez-Picado, J; Brodin, P; Nussenzweig, Mc; Boisson-Dupuis, S; Rodríguez-Gallego, C; Vogt, G; Mogensen, Th; Oler, Aj; Gu, J; Burbelo, Pd; Cohen, Ji; Biondi, A; Bettini, Lr; D'Angio, M; Bonfanti, P; Rossignol, P; Mayaux, J; Rieux-Laucat, F; Husebye, Es; Fusco, F; Ursini, Mv; Imberti, L; Sottini, A; Paghera, S; Quiros-Roldan, E; Rossi, C; Castagnoli, R; Montagna, D; Licari, A; Marseglia, Gl; Duval, X; Ghosn, J; Tsang, Js; Goldbach-Mansky, R; Kisand, K; Lionakis, Ms; Puel, A; Zhang, S; Holland, Sm; Gorochov, G; Jouanguy, E; Rice, Cm; Cobat, A; Notarangelo, Ld; Abel, L; Su, Hc; Casanova, J
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/288387
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