| Literature DB >> 34213846 |
Paul Bastard1,2,3, Qian Zhang2, Aurélie Cobat1,3, Emmanuelle Jouanguy1,2,3, Shen-Ying Zhang1,2,3, Laurent Abel1,2,3, Jean-Laurent Casanova4,1,2,3.
Abstract
We established the COVID Human Genetic Effort (www.covidhge.com) to discover the human genetic and immunological bases of the vast interindividual clinical variability between humans infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We found that about 3% of patients with life-threatening coronavirus disease 2019 (COVID-19) pneumonia were ill because of inborn errors of genes controlling type I interferon (IFN)-dependent immunity (which controls influenza virus), and at least 10% of patients with life-threatening COVID-19 pneumonia had neutralizing auto-Abs against some of the 17 individual type I IFNs. These findings indicate that impaired type I IFN immunity underlies life-threatening COVID-19 pneumonia in at least 13% of patients. These discoveries pave the way for further research into unexplained severe cases, and provide a rationale for preventing and treating the disease in individuals at risk, with recombinant type I IFNs.Entities:
Keywords: Autoantibodies; Inborn errors of immunity; Life-threatening COVID-19; Pneumonia; Type I interferons
Year: 2021 PMID: 34213846 DOI: 10.5802/crbiol.36
Source DB: PubMed Journal: C R Biol ISSN: 1631-0691 Impact factor: 1.583