학술논문

NFKB2 haploinsufficiency identified via screening for IFN-α2 autoantibodies in children and adolescents hospitalized with SARS-CoV-2–related complications
Document Type
article
Source
Journal of Allergy and Clinical Immunology. 151(4)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Lung
Vaccine Related
Infectious Diseases
Rare Diseases
Pneumonia
Clinical Research
Prevention
Emerging Infectious Diseases
Biodefense
Pediatric
Genetics
Autoimmune Disease
Aetiology
2.1 Biological and endogenous factors
Inflammatory and immune system
Good Health and Well Being
Adult
Humans
Child
Adolescent
SARS-CoV-2
COVID-19
Autoantibodies
NF-kappa B
Haploinsufficiency
Leukocytes
Mononuclear
Interferon Type I
NF-kappa B p52 Subunit
Anti-interferon autoantibody
MIS-C
NFKB2
inborn errors of immunity
Overcoming COVID-19 Network Study Group Investigators
Immunology
Allergy
Language
Abstract
BackgroundAutoantibodies against type I IFNs occur in approximately 10% of adults with life-threatening coronavirus disease 2019 (COVID-19). The frequency of anti-IFN autoantibodies in children with severe sequelae of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is unknown.ObjectiveWe quantified anti-type I IFN autoantibodies in a multicenter cohort of children with severe COVID-19, multisystem inflammatory syndrome in children (MIS-C), and mild SARS-CoV-2 infections.MethodsCirculating anti-IFN-α2 antibodies were measured by a radioligand binding assay. Whole-exome sequencing, RNA sequencing, and functional studies of peripheral blood mononuclear cells were used to study any patients with levels of anti-IFN-α2 autoantibodies exceeding the assay's positive control.ResultsAmong 168 patients with severe COVID-19, 199 with MIS-C, and 45 with mild SARS-CoV-2 infections, only 1 had high levels of anti-IFN-α2 antibodies. Anti-IFN-α2 autoantibodies were not detected in patients treated with intravenous immunoglobulin before sample collection. Whole-exome sequencing identified a missense variant in the ankyrin domain of NFKB2, encoding the p100 subunit of nuclear factor kappa-light-chain enhancer of activated B cells, aka NF-κB, essential for noncanonical NF-κB signaling. The patient's peripheral blood mononuclear cells exhibited impaired cleavage of p100 characteristic of NFKB2 haploinsufficiency, an inborn error of immunity with a high prevalence of autoimmunity.ConclusionsHigh levels of anti-IFN-α2 autoantibodies in children and adolescents with MIS-C, severe COVID-19, and mild SARS-CoV-2 infections are rare but can occur in patients with inborn errors of immunity.