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

被引:258
|
作者
Chang, Sarah Esther [1 ,2 ]
Feng, Allan [1 ,2 ]
Meng, Wenzhao [3 ]
Apostolidis, Sokratis A. [4 ,5 ]
Mack, Elisabeth [6 ]
Artandi, Maja [7 ,8 ]
Barman, Linda [7 ]
Bennett, Kate [9 ]
Chakraborty, Saborni [10 ]
Chang, Iris [2 ,11 ]
Cheung, Peggie [1 ,2 ]
Chinthrajah, Sharon [2 ,11 ]
Dhingra, Shaurya [1 ,2 ]
Do, Evan [2 ,11 ]
Finck, Amanda [12 ]
Gaano, Andrew [3 ]
Gessner, Reinhard [13 ]
Giannini, Heather M. [14 ]
Gonzalez, Joyce [3 ]
Greib, Sarah [13 ]
Guendisch, Margrit [13 ]
Hsu, Alex Ren [1 ,2 ]
Kuo, Alex [1 ,2 ]
Manohar, Monali [2 ,10 ]
Mao, Rong [1 ,2 ]
Neeli, Indira [14 ]
Neubauer, Andreas [6 ]
Oniyide, Oluwatosin [15 ]
Powell, Abigail Elizabeth [16 ,17 ]
Puri, Rajan [7 ]
Renz, Harald [13 ,18 ,19 ]
Schapiro, Jeffrey M. [20 ]
Weidenbacher, Payton A. [16 ,17 ]
Wittman, Rich [7 ]
Ahuja, Neera [21 ]
Chung, Ho-Ryun [22 ]
Jagannathan, Pras [2 ,10 ,23 ]
James, Judith [24 ]
Kim, Peter S. [14 ,16 ,25 ]
Meyer, Nuala J. [5 ,15 ]
Nadeau, Kari [2 ,11 ]
Radic, Marko [14 ]
Robinson, William H. [1 ,2 ,26 ]
Singh, Upinder [2 ,10 ,23 ]
Wang, Taia T. [10 ,23 ,25 ]
Wherry, E. John [5 ,12 ]
Skevaki, Chrysanthi [13 ,18 ,19 ]
Prak, Eline T. Luning [3 ,5 ]
Utz, Pj [1 ,2 ]
机构
[1] Stanford Univ, Dept Med, Div Immunol & Rheumatol, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Inst Immun Transplantat & Infect, Stanford, CA 94305 USA
[3] Univ Penn, Dept Pathol & Lab, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] Univ Penn, Perelman Sch Med, Dept Med, Div Rheumatol, Philadelphia, PA 19104 USA
[5] Univ Penn, Perelman Sch Med, Inst Immunol, Philadelphia, PA 19104 USA
[6] Philipps Univ Marburg, Dept Hematol Oncol Immunol, Marburg, Germany
[7] Stanford Univ, Dept Med, Div Primary Care & Populat Hlth, Sch Med, Stanford, CA 94305 USA
[8] Stanford Univ, Sch Med, Dept Med, Stanford CROWN Clin, Stanford, CA 94305 USA
[9] Univ Penn, Dept Med, Mol Pathol & Imaging Core, Gastroenterol Div,Perelman Sch Med, Philadelphia, PA 19104 USA
[10] Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Sch Med, Stanford, CA 94305 USA
[11] Stanford Univ, Sean N Parker Ctr Allergy & Asthma Res, Sch Med, Dept Med, Stanford, CA 94305 USA
[12] Univ Penn, Perelman Sch Med, Dept Syst Pharmacol & Translat Therapeut, Philadelphia, PA 19104 USA
[13] Philipps Univ Marburg, Inst Lab Med, Marburg, Germany
[14] Univ Tennessee, Dept Microbiol Immunol & Biochem, Hlth Sci Ctr, Memphis, TN USA
[15] Univ Penn, Dept Med, Div Pulm Allergy & Crit Care Med, Perelman Sch Med, Philadelphia, PA 19104 USA
[16] Stanford Univ, Dept Biochem, Sch Med, Stanford, CA 94305 USA
[17] Stanford Univ, ChEM H, Stanford, CA 94305 USA
[18] Univ Giessen & Marburg Lung Ctr UGMLC, Giessen, Germany
[19] German Ctr Lung Res DZL, Giessen, Germany
[20] Kaiser Permanente Northern Calif, TPMG Reg Reference Lab, Berkeley, CA USA
[21] Stanford Univ, Dept Med, Div Hosp Med, Sch Med, Stanford, CA 94305 USA
[22] Philipps Univ Marburg, Inst Med Bioinformat & Biostat, Marburg, Germany
[23] Stanford Univ, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[24] Oklahoma Med Res Fdn, Arthrit & Clin Immunol Program, 825 NE 13th St, Oklahoma City, OK 73104 USA
[25] Chan Zuckerberg Biohub, San Francisco, CA USA
[26] VA Palo Alto Hlth Care Syst, Palo Alto, CA USA
基金
美国国家卫生研究院;
关键词
ANTIBODY-RESPONSES; AUTOANTIGENS; ACTIVATION; PROTEIN; VIRUS;
D O I
10.1038/s41467-021-25509-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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. Infection with SARS-CoV2 and the development of Coronavirus disease 2019 (COVID-19) has been linked to induction of autoimmunity and autoantibody production. Here the authors characterise the new-onset IgG autoantibody response in hospitalised patients with COVID-19 which they correlate to the magnitude of the SARS-CoV2 response.
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页数:15
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