Abstract
Circulating autoantibodies (auto-Abs) neutralizing high concentrations (10 ng/ml; in plasma diluted 1:10) of IFN-α and/or IFN-ω are found in about 10% of patients with critical COVID-19 (coronavirus disease 2019) pneumonia but not in individuals with asymptomatic infections. We detect auto-Abs neutralizing 100-fold lower, more physiological, concentrations of IFN-α and/or IFN-ω (100 pg/ml; in 1:10 dilutions of plasma) in 13.6% of 3595 patients with critical COVID-19, including 21% of 374 patients >80 years, and 6.5% of 522 patients with severe COVID-19. These antibodies are also detected in 18% of the 1124 deceased patients (aged 20 days to 99 years; mean: 70 years). Moreover, another 1.3% of patients with critical COVID-19 and 0.9% of the deceased patients have auto-Abs neutralizing high concentrations of IFN-β. We also show, in a sample of 34,159 uninfected individuals from the general population, that auto-Abs neutralizing high concentrations of IFN-α and/or IFN-ω are present in 0.18% of individuals between 18 and 69 years, 1.1% between 70 and 79 years, and 3.4% >80 years. Moreover, the proportion of individuals carrying auto-Abs neutralizing lower concentrations is greater in a subsample of 10,778 uninfected individuals: 1% of individuals <70 years, 2.3% between 70 and 80 years, and 6.3% >80 years. By contrast, auto-Abs neutralizing IFN-β do not become more frequent with age. Auto-Abs neutralizing type I IFNs predate SARS-CoV-2 infection and sharply increase in prevalence after the age of 70 years. They account for about 20% of both critical COVID-19 cases in the over 80s and total fatal COVID-19 cases.
Original language | English |
---|---|
Article number | eabl4340 |
Journal | Science immunology |
Volume | 6 |
Issue number | 62 |
DOIs | |
State | Published - Aug 19 2021 |
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Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths. / NIAID Immune Response to COVID Group; Danish CHGE; COVID Human Genetic Effort et al.
In: Science immunology, Vol. 6, No. 62, eabl4340, 19.08.2021.Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths
AU - NIAID Immune Response to COVID Group
AU - Danish CHGE
AU - COVID Human Genetic Effort
AU - HGID Lab
AU - COVID-STORM Clinicians
AU - NH-COVAIR Study Group
AU - The Danish Blood Donor Study (DBDS)
AU - Imagine COVID Group
AU - The Milieu Intérieur Consortium
AU - Amsterdam UMC Covid-19 Biobank
AU - CONSTANCES cohort
AU - 3C-Dijon Study
AU - Cerba HealthCare
AU - Etablissement du Sang study group
AU - CoV-Contact Cohort
AU - St James's Hospital, SARS CoV2 Interest group
AU - COVID Clinicians
AU - French COVID Cohort Study Group
AU - Bastard, Paul
AU - Gervais, Adrian
AU - Voyer, Tom Le
AU - Rosain, Jérémie
AU - Philippot, Quentin
AU - Manry, Jérémy
AU - Michailidis, Eleftherios
AU - Hoffmann, Hans Heinrich
AU - Eto, Shohei
AU - Garcia-Prat, Marina
AU - Bizien, Lucy
AU - Parra-Martínez, Alba
AU - Yang, Rui
AU - Haljasmägi, Liis
AU - Migaud, Mélanie
AU - Särekannu, Karita
AU - Maslovskaja, Julia
AU - De Prost, Nicolas
AU - Tandjaoui-Lambiotte, Yacine
AU - Luyt, Charles Edouard
AU - Amador-Borrero, Blanca
AU - Gaudet, Alexandre
AU - Poissy, Julien
AU - Morel, Pascal
AU - Richard, Pascale
AU - Cognasse, Fabrice
AU - Troya, Jesus
AU - Trouillet-Assant, Sophie
AU - Belot, Alexandre
AU - Saker, Kahina
AU - Garçon, Pierre
AU - Rivière, Jacques G.
AU - Lagier, Jean Christophe
AU - Gentile, Stéphanie
AU - Rosen, Lindsey B.
AU - Shaw, Elana
AU - Morio, Tomohiro
AU - Tanaka, Junko
AU - Dalmau, David
AU - Tharaux, Pierre Louis
AU - Sene, Damien
AU - Stepanian, Alain
AU - Megarbane, Bruno
AU - Triantafyllia, Vasiliki
AU - Fekkar, Arnaud
AU - Heath, James R.
AU - Franco, José Luis
AU - Anaya, Juan Manuel
AU - Solé-Violán, Jordi
AU - Imberti, Luisa
AU - Biondi, Andrea
AU - Bonfanti, Paolo
AU - Castagnoli, Riccardo
AU - Delmonte, Ottavia M.
AU - Zhang, Yu
AU - Snow, Andrew L.
AU - Holland, Steven M.
AU - Biggs, Catherine M.
AU - Moncada-Vélez, Marcela
AU - Arias, Andrés Augusto
AU - Lorenzo, Lazaro
AU - Boucherit, Soraya
AU - Coulibaly, Boubacar
AU - Anglicheau, Dany
AU - Planas, Anna M.
AU - Haerynck, Filomeen
AU - Duvlis, Sotirija
AU - Nussbaum, Robert L.
AU - Ozcelik, Tayfun
AU - Keles, Sevgi
AU - Bousfiha, Ahmed A.
AU - El Bakkouri, Jalila
AU - Ramirez-Santana, Carolina
AU - Paul, Stéphane
AU - Pan-Hammarström, Qiang
AU - Hammarström, Lennart
AU - Dupont, Annabelle
AU - Kurolap, Alina
AU - Metz, Christine N.
AU - Aiuti, Alessandro
AU - Casari, Giorgio
AU - Lampasona, Vito
AU - Ciceri, Fabio
AU - Barreiros, Lucila A.
AU - Dominguez-Garrido, Elena
AU - Vidigal, Mateus
AU - Zatz, Mayana
AU - Van De Beek, Diederik
AU - Sahanic, Sabina
AU - Tancevski, Ivan
AU - Stepanovskyy, Yurii
AU - Boyarchuk, Oksana
AU - Nukui, Yoko
AU - Tsumura, Miyuki
AU - Vidaur, Loreto
AU - Tangye, Stuart G.
AU - Burrel, Sonia
AU - Duffy, Darragh
AU - Quintana-Murci, Lluis
AU - Klocperk, Adam
AU - Kann, Nelli Y.
AU - Shcherbina, Anna
AU - Lau, Yu Lung
AU - Leung, Daniel
AU - Coulongeat, Matthieu
AU - Marlet, Julien
AU - Koning, Rutger
AU - Reyes, Luis Felipe
AU - Chauvineau-Grenier, Angélique
AU - Venet, Fabienne
AU - Monneret, Guillaume
AU - Nussenzweig, Michel C.
AU - Arrestier, Romain
AU - Boudhabhay, Idris
AU - Baris-Feldman, Hagit
AU - Hagin, David
AU - Wauters, Joost
AU - Meyts, Isabelle
AU - Dyer, Adam H.
AU - Kennelly, Sean P.
AU - Bourke, Nollaig M.
AU - Halwani, Rabih
AU - Sharif-Askari, Narjes Saheb
AU - Dorgham, Karim
AU - Sallette, Jérome
AU - Sedkaoui, Souad Mehlal
AU - AlKhater, Suzan
AU - Rigo-Bonnin, Raúl
AU - Morandeira, Francisco
AU - Roussel, Lucie
AU - Vinh, Donald C.
AU - Ostrowski, Sisse Rye
AU - Condino-Neto, Antonio
AU - Prando, Carolina
AU - Bondarenko, Anastasiia
AU - Spaan, András N.
AU - Gilardin, Laurent
AU - Fellay, Jacques
AU - Lyonnet, Stanislas
AU - Bilguvar, Kaya
AU - Lifton, Richard P.
AU - Mane, Shrikant
AU - Anderson, Mark S.
AU - Boisson, Bertrand
AU - Béziat, Vivien
AU - Zhang, Shen Ying
AU - Andreakos, Evangelos
AU - Hermine, Olivier
AU - Pujol, Aurora
AU - Peterson, Pärt
AU - Mogensen, Trine H.
AU - Rowen, Lee
AU - Mond, James
AU - Debette, Stéphanie
AU - De Lamballerie, Xavier
AU - Duval, Xavier
AU - Mentré, France
AU - Zins, Marie
AU - Soler-Palacin, Pere
AU - Colobran, Roger
AU - Gorochov, Guy
AU - Solanich, Xavier
AU - Susen, Sophie
AU - Martinez-Picado, Javier
AU - Raoult, Didier
AU - Vasse, Marc
AU - Gregersen, Peter K.
AU - Piemonti, Lorenzo
AU - Rodríguez-Gallego, Carlos
AU - Notarangelo, Luigi D.
AU - Su, Helen C.
AU - Kisand, Kai
AU - Okada, Satoshi
AU - Puel, Anne
AU - Jouanguy, Emmanuelle
AU - Rice, Charles M.
AU - Tiberghien, Pierre
AU - Zhang, Qian
AU - Cobat, Aurélie
AU - Abel, Laurent
AU - Casanova, Jean Laurent
AU - Alavoine, Loubna
AU - Behillil, Sylvie
AU - Burdet, Charles
AU - Charpentier, Charlotte
AU - Dechanet, Aline
AU - Descamps, Diane
AU - Ecobichon, Jean Luc
AU - Enouf, Vincent
AU - Frezouls, Wahiba
AU - Houhou, Nadhira
AU - Kafif, Ouifiya
AU - Lehacaut, Jonathan
AU - Letrou, Sophie
AU - Lina, Bruno
AU - Lucet, Jean Christophe
AU - Manchon, Pauline
AU - Nouroudine, Mariama
AU - Piquard, Valentine
AU - Cooper, Megan A.
N1 - Funding Information: Funding: The Laboratory of Human Genetics of Infectious Diseases is supported by the Howard Hughes Medical Institute, the Rockefeller University, the St. Giles Foundation, the National Institutes of Health (NIH) (R01AI088364), the National Center for Advancing Translational Sciences (NCATS), NIH Clinical and Translational Science Awards (CTSA) program (UL1 TR001866), a Fast Grant from Emergent Ventures, Mercatus Center at George Mason University, the Yale Center for Mendelian Genomics and the GSP Coordinating Center funded by the National Human Genome Research Institute (NHGRI) (UM1HG006504 and U24HG008956), the Yale High Performance Computing Center (S10OD018521), the Fisher Center for Alzheimer’s Research Foundation, the Meyer Foundation, the JPB Foundation, the French National Research Agency (ANR) under the “Investments for the Future” program (ANR-10-IAHU-01), the Integrative Biology of Emerging Infectious Diseases Laboratory of Excellence (ANR-10-LABX-62-IBEID), the French Foundation for Medical Research (FRM) (EQU201903007798), the FRM and ANR GENCOVID project (ANR-20-COVI-0003), ANRS Nord-Sud (ANRS-COV05), ANR GENVIR (ANR-20-CE93-003) and ANR AABIFNCOV (ANR-20-CO11-0001) projects, the European Union’s Horizon 2020 research and innovation programme under grant agreement no. 824110 (EASI-Genomics), the Square Foundation, Grandir–Fonds de solidarité pour l’Enfance, the Fondation du Souffle, the SCOR Corporate Foundation for Science, Institut National de la Santé et de la Recherche Médicale (INSERM), REACTing-INSERM; and the University of Paris. P.B. was supported by the FRM (EA20170638020). P.B., J.R., and T.L.V. were supported by the MD-PhD program of the Imagine Institute (with the support of the Fondation Bettencourt Schueller). Work in the Laboratory of Virology and Infectious Disease was supported by the NIH (P01AI138398-S1, 2U19AI111825, and R01AI091707-10S1), a George Mason University Fast Grant, and the G. Harold and Leila Y. Mathers Charitable Foundation. The French COVID Cohort study group was sponsored by INSERM and supported by the REACTing consortium and by a grant from the French Ministry of Health (PHRC 20-0424). The Cov-Contact Cohort was supported by the REACTing consortium, the French Ministry of Health, and the European Commission (RECOVER WP 6). This work was also partly supported by the Intramural Research Program of the NIAID and NIDCR, NIH (grants ZIA AI001270 to L.D.N. and 1ZIAAI001265 to H.C.S.). This program is supported by the Agence Nationale de la Recherche (reference ANR-10-LABX-69-01). K.K.’s group was supported by the Estonian Research Council grants PRG117 and PRG377. R.H. was supported by an Al Jalila Foundation Seed Grant (AJF202019), Dubai, UAE, and a COVID-19 research grant (CoV19-0307) from the University of Sharjah, UAE. S.G.T. is supported by Investigator and Program Grants awarded by the National Health and Medical Research Council of Australia and a UNSW Sydney COVID Rapid Response Initiative Grant. L.I. reported funding from Regione Lombardia, Italy (project “Risposta immune in pazienti con COVID-19 e co-morbidità”). L.I. and G. L. Marseglia reported funding from Regione Lombardia, Italy (project Risposta immune in pazienti con COVID-19 e co-morbidità). This research was partially supported by the Instituto de Salud Carlos III (COV20/0968). J.R.H. reported funding from Biomedical Advanced Research and Development Authority HHSO10201600031C. S.O. reports funding Research Program on Emerging and Re-emerging Infectious Diseases from Japan Agency for Medical Research and Development, AMED (grant number JP20fk0108531). G.G. was supported by ANR Flash COVID-19 program and SARS-CoV-2 Program of the Faculty of Medicine from Sorbonne University iCOVID programs. The Three-City (3C) Study was conducted under a partnership agreement among the INSERM, the Victor Segalen Bordeaux 2 University, and Sanofi-Aventis. The Fondation pour la Recherche Médicale funded the preparation and initiation of the study. The 3C Study was also supported by the Caisse Nationale d’Assurance Maladie des Travailleurs Salariés, Direction générale de la Santé, Mutuelle Générale de l’Education Nationale (MGEN), Institut de la Longévité, Conseils Régionaux of Aquitaine and Bourgogne, Fondation de France, and Ministry of Research–INSERM Programme “Cohortes et collections de données biologiques”. S. Debette was supported by the University of Bordeaux Initiative of Excellence. P.K.G. reports funding from the National Cancer Institute, NIH, under contract no. 75N91019D00024, task order no. 75N91021F00001. J.W. is supported by an FWO Fundamental Clinical Mandate (1833317N). Sample processing at IrsiCaixa was possible thanks to the crowdfunding initiative YoMeCorono. Work at Vall d’Hebron was also partly supported by research funding from Instituto de Salud Carlos III grant PI17/00660 cofinanced by the European Regional Development Fund (ERDF). C.R.-G. and colleagues of the Canarian Health System Sequencing Hub were supported by the Instituto de Salud Carlos III (COV20_01333 and COV20_01334, Spanish Ministry for Science and Innovation RTC-2017-6471-1; AEI/FEDER, UE), Fundación DISA (OA18/017 and OA20/024), and Cabildo Insular de Tenerife (CGIEU0000219140 and “Apuestas científicas del ITER para colaborar en la lucha contra la COVID-19”). C.M.B. is supported by a MSFHR Health Professional-Investigator Award. P.Q.H. and L.H. were funded by the European Union’s Horizon 2020 research and innovation program (ATAC, 101003650). Work at Y.-L.L.’s laboratory in the University of Hong Kong (HKU) was supported by the Society for the Relief of Disabled Children. MBBS/PhD study of D.L. in HKU was supported by the Croucher Foundation. J.L.F. was supported in part by the Coopération Scientifique France-Colciencias (ECOS-Nord/ COLCIENCIAS/MEN/ICETEX (806-2018) and Colciencias contract 713-2016 (code 111574455633)]. A.K. was in part supported by grants NU20-05-00282 and NV18-05-00162 issued by the Czech Health Research Council and Ministry of Health, Czech Republic. L.P. was funded by Program Project COVID-19 OSR-UniSR and Ministero della Salute (COVID-2020-12371617). I.M. is a Senior Clinical Investigator at the Research Foundation–Flanders and is supported by the CSL Behring Chair of Primary Immunodeficiencies; by the KU Leuven C1 grant C16/18/007; by a VIB-GC PID grant; by the FWO frants G0C8517N, G0B5120N, and G0E8420N; and by the Jeffrey Modell Foundation. I.M. has received funding under the European Union’s Horizon 2020 research and innovation programme (grant agreement no. 948959). E.A. received funding from the Hellenic Foundation for Research and Innovation (INTERFLU, no. 1574). M.Vi received funding from the São Paulo Research Foundation (FAPESP) (grant number 2020/09702-1) and JBS SA (grant number 69004). The NH-COVAIR study group consortium was supported by a grant from the Meath Foundation. Publisher Copyright: © 2021 The Authors, some rights reserved.
PY - 2021/8/19
Y1 - 2021/8/19
N2 - Circulating autoantibodies (auto-Abs) neutralizing high concentrations (10 ng/ml; in plasma diluted 1:10) of IFN-α and/or IFN-ω are found in about 10% of patients with critical COVID-19 (coronavirus disease 2019) pneumonia but not in individuals with asymptomatic infections. We detect auto-Abs neutralizing 100-fold lower, more physiological, concentrations of IFN-α and/or IFN-ω (100 pg/ml; in 1:10 dilutions of plasma) in 13.6% of 3595 patients with critical COVID-19, including 21% of 374 patients >80 years, and 6.5% of 522 patients with severe COVID-19. These antibodies are also detected in 18% of the 1124 deceased patients (aged 20 days to 99 years; mean: 70 years). Moreover, another 1.3% of patients with critical COVID-19 and 0.9% of the deceased patients have auto-Abs neutralizing high concentrations of IFN-β. We also show, in a sample of 34,159 uninfected individuals from the general population, that auto-Abs neutralizing high concentrations of IFN-α and/or IFN-ω are present in 0.18% of individuals between 18 and 69 years, 1.1% between 70 and 79 years, and 3.4% >80 years. Moreover, the proportion of individuals carrying auto-Abs neutralizing lower concentrations is greater in a subsample of 10,778 uninfected individuals: 1% of individuals <70 years, 2.3% between 70 and 80 years, and 6.3% >80 years. By contrast, auto-Abs neutralizing IFN-β do not become more frequent with age. Auto-Abs neutralizing type I IFNs predate SARS-CoV-2 infection and sharply increase in prevalence after the age of 70 years. They account for about 20% of both critical COVID-19 cases in the over 80s and total fatal COVID-19 cases.
AB - Circulating autoantibodies (auto-Abs) neutralizing high concentrations (10 ng/ml; in plasma diluted 1:10) of IFN-α and/or IFN-ω are found in about 10% of patients with critical COVID-19 (coronavirus disease 2019) pneumonia but not in individuals with asymptomatic infections. We detect auto-Abs neutralizing 100-fold lower, more physiological, concentrations of IFN-α and/or IFN-ω (100 pg/ml; in 1:10 dilutions of plasma) in 13.6% of 3595 patients with critical COVID-19, including 21% of 374 patients >80 years, and 6.5% of 522 patients with severe COVID-19. These antibodies are also detected in 18% of the 1124 deceased patients (aged 20 days to 99 years; mean: 70 years). Moreover, another 1.3% of patients with critical COVID-19 and 0.9% of the deceased patients have auto-Abs neutralizing high concentrations of IFN-β. We also show, in a sample of 34,159 uninfected individuals from the general population, that auto-Abs neutralizing high concentrations of IFN-α and/or IFN-ω are present in 0.18% of individuals between 18 and 69 years, 1.1% between 70 and 79 years, and 3.4% >80 years. Moreover, the proportion of individuals carrying auto-Abs neutralizing lower concentrations is greater in a subsample of 10,778 uninfected individuals: 1% of individuals <70 years, 2.3% between 70 and 80 years, and 6.3% >80 years. By contrast, auto-Abs neutralizing IFN-β do not become more frequent with age. Auto-Abs neutralizing type I IFNs predate SARS-CoV-2 infection and sharply increase in prevalence after the age of 70 years. They account for about 20% of both critical COVID-19 cases in the over 80s and total fatal COVID-19 cases.
UR - http://www.scopus.com/inward/record.url?scp=85113517428&partnerID=8YFLogxK
U2 - 10.1126/sciimmunol.abl4340
DO - 10.1126/sciimmunol.abl4340
M3 - Article
C2 - 34413139
AN - SCOPUS:85113517428
SN - 2470-9468
VL - 6
JO - Science Immunology
JF - Science Immunology
IS - 62
M1 - eabl4340
ER -