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

Sarah E. Chang(Stanford University), Allan Feng(Stanford University), Wenzhao Meng(University of Pennsylvania), Sokratis A. Apostolidis(University of Pennsylvania), Elisabeth Mack(Philipps University of Marburg), Maja Artandi(Stanford University), Linda Barman(Stanford University), Kate Bennett(University of Pennsylvania), Saborni Chakraborty(Stanford University), Iris Chang(Stanford University), Peggie Cheung(Stanford University), R. Sharon Chinthrajah(Stanford University), Shaurya Dhingra(Stanford University), Evan Do(Stanford University), Amanda Finck(Translational Therapeutics (United States)), Andrew Gaano(University of Pennsylvania), Reinhard Geßner(Philipps University of Marburg), H.M. Giannini(University of Tennessee Health Science Center), Joyce González(University of Pennsylvania), Sarah Greib(Philipps University of Marburg), Margrit Gündisch(Philipps University of Marburg), Alexander Hsu(Stanford University), Alex Kuo(Stanford University), Monali Manohar(Stanford University), Rong Mao(Stanford University), Indira Neeli(University of Tennessee Health Science Center), Andreas Neubauer(Philipps University of Marburg), Oluwatosin Oniyide(University of Pennsylvania), Abigail E. Powell(Stanford University), Rajan Puri(Stanford University), Harald Renz(Philipps University of Marburg), Jeffrey M. Schapiro(Kaiser Permanente), Payton A. Weidenbacher(Stanford University), Richard Wittman(Stanford University), Neera Ahuja(Stanford Medicine), Ho‐Ryun Chung(Philipps University of Marburg), Prasanna Jagannathan(Stanford University), Judith A. James(Oklahoma Medical Research Foundation), Peter S. Kim(University of Tennessee Health Science Center), Nuala J. Meyer(University of Pennsylvania), Kari C. Nadeau(Stanford University), Marko Radic(University of Tennessee Health Science Center), William H. Robinson(VA Palo Alto Health Care System), Upinder Singh(Stanford University), Taia T. Wang(Chan Zuckerberg Initiative (United States)), E. John Wherry(Translational Therapeutics (United States)), Chrysanthi Skevaki(Philipps University of Marburg), Eline T. Luning Prak(University of Pennsylvania), Paul J. Utz(Stanford Medicine)
Nature Communications
September 14, 2021
Cited by 463Open Access
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Abstract

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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