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  4. Screening and characterization of myositis-related autoantibodies in COVID-19 patients
 
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Screening and characterization of myositis-related autoantibodies in COVID-19 patients

Journal
Clinical and translational science
Journal Volume
16
Journal Issue
1
Date Issued
2023-01
Author(s)
Teo, Kai-Fa
Chen, Der-Yuan
Hsu, Jeh-Ting
Lai, Yi-Hua
Chang, Ching-Kun
PO-REN HSUEH  
Lan, Joung-Liang
Hsu, Jye-Lin
DOI
10.1111/cts.13434
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/628084
URL
https://api.elsevier.com/content/abstract/scopus_id/85141430698
Abstract
An efficient host immune response against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, COVID-19) appears to be crucial for controlling and resolving this viral infection. However, many studies have reported autoimmune characteristics in severe COVID-19 patients. Moreover, clinical observations have revealed that COVID-19-associated acute distress respiratory syndrome shares many features in common with inflammatory myopathy including interstitial lung disease (ILD), most particularly rapidly progressive (RP)-ILD. This study explored this phenomenon by seeking to identify and characterize myositis-specific and related autoantibodies in 25 COVID-19 patients with mild or severe symptoms. Line blot analysis with the EUROLINE Myopathies Ag kit identified 9 (36%) patients with COVID-19 with one or more autoantibodies against several myositis-related antigens (Jo-1, Ku, Mi-2β, PL-7, PL-12, PM-Scl 75, PM-Scl 100, Ro-52, and SRP); no anti-MDA5 antibodies were detected. As the presence of antibodies identified by line blots was unrelated to disease severity, we further characterized the autoantibodies by radioimmunoassay, in which [35 S]methionine-labeled K562 cellular antigens were precipitated and visualized by gel electrophoresis. This result was confirmed by an immunoprecipitation assay and immunoblotting; 2 patients exhibited anti-Ku70 and anti-Ku80 antibodies. Our data suggest that it is necessary to use more than one method to characterize and evaluate autoantibodies in people recovered from COVID-19, in order to avoid misinterpreting those autoantibodies as diagnostic markers for autoimmune diseases.
Subjects
GENE 5; JAPANESE PATIENTS; ANTIBODIES; ASSOCIATION; DERMATOMYOSITIS
SDGs

[SDGs]SDG3

Publisher
WILEY
Type
journal article

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