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DOI 10.1038/s41467-021-25509-3

Медицинская библиотека · Nature communications · 2021

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

Chang Sarah Esther, Feng Allan, Meng Wenzhao, Apostolidis Sokratis A, Mack Elisabeth, Artandi Maja, Barman Linda, Bennett Kate, Chakraborty Saborni, Chang Iris, Cheung Peggie, Chinthrajah Sharon, Dhingra Shaurya, Do Evan, Finck Amanda, Gaano Andrew, Geßner Reinhard, Giannini Heather M, Gonzalez Joyce, Greib Sarah, Gündisch Margrit, Hsu Alex Ren, Kuo Alex, Manohar Monali, Mao Rong, Neeli Indira, Neubauer Andreas, Oniyide Oluwatosin, Powell Abigail E, Puri Rajan, Renz Harald, Schapiro Jeffrey, Weidenbacher Payton A, Wittman Richard, Ahuja Neera, Chung Ho-Ryun, Jagannathan Prasanna, James Judith A, Kim Peter S, Meyer Nuala J, Nadeau Kari C, Radic Marko, Robinson William H, Singh Upinder, Wang Taia T, Wherry E John, Skevaki Chrysanthi, Luning Prak Eline T, Utz Paul J

СтатьяМногоцентровое исследованиеПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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.

Для цитирования: Chang Sarah Esther, Feng Allan, Meng Wenzhao, Apostolidis Sokratis A, Mack Elisabeth, Artandi Maja, Barman Linda, Bennett Kate, Chakraborty Saborni, Chang Iris, Cheung Peggie, Chinthrajah Sharon, Dhingra Shaurya, Do Evan, Finck Amanda, Gaano Andrew, Geßner Reinhard, Giannini Heather M, Gonzalez Joyce, Greib Sarah, Gündisch Margrit, Hsu Alex Ren, Kuo Alex, Manohar Monali, Mao Rong, Neeli Indira, Neubauer Andreas, Oniyide Oluwatosin, Powell Abigail E, Puri Rajan, Renz Harald, Schapiro Jeffrey, Weidenbacher Payton A, Wittman Richard, Ahuja Neera, Chung Ho-Ryun, Jagannathan Prasanna, James Judith A, Kim Peter S, Meyer Nuala J, Nadeau Kari C, Radic Marko, Robinson William H, Singh Upinder, Wang Taia T, Wherry E John, Skevaki Chrysanthi, Luning Prak Eline T, Utz Paul J. New-onset IgG autoantibodies in hospitalized patients with COVID-19.. Nature communications. 2021. DOI: 10.1038/s41467-021-25509-3.

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