Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Inserm U1163, Necker Hospital for Sick Children, Paris, France.
St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.
C R Biol. 2021 Jun 21;344(1):19-25. doi: 10.5802/crbiol.36.
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.
我们成立了 COVID 人类遗传研究计划(www.covidhge.com),旨在发现人类感染严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)后个体间临床表现差异巨大的人类遗传和免疫学基础。我们发现,约 3%的有生命危险的 2019 冠状病毒病(COVID-19)肺炎患者因控制 I 型干扰素(IFN)依赖性免疫(控制流感病毒)的基因先天缺陷而患病,至少 10%的有生命危险的 COVID-19 肺炎患者对 17 种单独的 I 型 IFN 中的一些具有中和自身抗体。这些发现表明,至少 13%的有生命危险的 COVID-19 肺炎患者的 I 型 IFN 免疫受损。这些发现为进一步研究不明原因的严重病例铺平了道路,并为使用重组 I 型 IFN 预防和治疗高危个体的疾病提供了依据。