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New-onset IgG autoantibodies in hospitalized patients with COVID-19.

Sarah Esther ChangAllan FengWenzhao MengSokratis A ApostolidisElisabeth K M MackMaja ArtandiLinda BarmanKate BennettSaborni ChakrabortyIris ChangPeggie CheungSharon ChinthrajahShaurya DhingraEvan DoAmanda FinckAndrew GaanoReinhard GeßnerHeather M GianniniJoyce GonzalezSarah GreibMargrit GündischAlex Ren HsuAlex J KuoMonali ManoharRong MaoIndira NeeliAndreas NeubauerOluwatosin OniyideAbigail E PowellRajan PuriHarald RenzJeffrey SchapiroPayton A WeidenbacherRichard WittmanNeera AhujaHo-Ryun ChungPrasanna JagannathanJudith A JamesPeter S KimNuala J MeyerKari Christine NadeauMarko Z RadicWilliam H RobinsonUpinder SinghTaia T WangE John WherryChrysanthi SkevakiEline T Luning PrakPaul J Utz
Published in: Nature communications (2021)
COVID-19 is associated with a wide range of clinical manifestations, including autoimmune features and autoantibody production. Here we develop three protein arrays to measure IgG autoantibodies associated with connective tissue diseases, anti-cytokine antibodies, and anti-viral antibody responses in serum from 147 hospitalized COVID-19 patients. Autoantibodies are identified in approximately 50% of patients but in less than 15% of healthy controls. When present, autoantibodies largely target autoantigens associated with rare disorders such as myositis, systemic sclerosis and overlap syndromes. A subset of autoantibodies targeting traditional autoantigens or cytokines develop de novo following SARS-CoV-2 infection. Autoantibodies track with longitudinal development of IgG antibodies recognizing SARS-CoV-2 structural proteins and a subset of non-structural proteins, but not proteins from influenza, seasonal coronaviruses or other pathogenic viruses. We conclude that SARS-CoV-2 causes development of new-onset IgG autoantibodies in a significant proportion of hospitalized COVID-19 patients and are positively correlated with immune responses to SARS-CoV-2 proteins.
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