4.6 Article

Patients with severe COVID-19 do not have elevated autoantibodies against common diagnostic autoantigens

Journal

CLINICAL CHEMISTRY AND LABORATORY MEDICINE
Volume 60, Issue 7, Pages 1116-1123

Publisher

WALTER DE GRUYTER GMBH
DOI: 10.1515/cclm-2022-0239

Keywords

autoantibodies; autoimmunity; COVID-19; electrochemiluminescence; Intensive care unit (ICU); prognostic markers; SARS-CoV-2; severe disease

Funding

  1. National Institute of Allergy and Infectious Diseases of the National Institutes of Health [U24AI118660]

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This study investigated the presence of autoantibodies in COVID-19 patients and found no significant elevation of autoantibodies in severe cases.
Objectives: Infection by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the causative pathogen of coronavirus disease 2019 (COVID-19) presents occasionally with an aberrant autoinflammatory response, including the presence of elevated circulating autoantibodies in some individuals. Whether the development of autoantibodies against self-antigens affects COVID-19 outcomes remains unclear. To better understand the prognostic role of autoantibodies in COVID-19, we quantified autoantibodies against 23 markers that are used for diagnosis of autoimmune disease. To this end, we used serum samples from patients with severe [intensive care unit (ICU)] and moderate (ward) COVID-19, across two to six consecutive time points, and compared autoantibody levels to uninfected healthy and ICU controls. Methods: Acute and post-acute serum (from 1 to 26 ICU days) was collected from 18 ICU COVID-19-positive patients at three to six time points; 18 ICU COVID-19-negative patients (sampled on ICU day 1 and 3); 21 ward COVID-19-positive patients (sampled on hospital day 1 and 3); and from 59 healthy uninfected controls deriving from two cohorts. Levels of IgG autoantibodies against 23 autoantigens, commonly used for autoimmune disease diagnosis, were measured in serum samples using MSD (R) U-PLEX electrochemiluminescence technology (MSD division Meso Scale Discovery (R)), and results were compared between groups. Results: There were no significant elevations of autoantibodies for any of the markers tested in patients with severe COVID-19. Conclusions: Sample collections at longer time points should be considered in future studies, for assessing the possible development of autoantibody responses following infection with SARS-CoV-2.

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