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SARS-CoV-2 infection is associated with anti-desmoglein 2 autoantibody detection.
Ward, Kerensa E; Steadman, Lora; Karim, Abid R; Reynolds, Gary M; Pugh, Matthew; Chua, Winnie; Faustini, Sian E; Veenith, Tonny; Thwaites, Ryan S; Openshaw, Peter J M; Drayson, Mark T; Shields, Adrian M; Cunningham, Adam F; Wraith, David C; Richter, Alex G.
Affiliation
  • Ward KE; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, West Midlands, UK.
  • Steadman L; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, West Midlands, UK.
  • Karim AR; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, West Midlands, UK.
  • Reynolds GM; Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, West Midlands, UK.
  • Pugh M; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, West Midlands, UK.
  • Chua W; Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, West Midlands, UK.
  • Faustini SE; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, West Midlands, UK.
  • Veenith T; Department of Critical Care, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Thwaites RS; National Heart and Lung Institute, Imperial College London, London, UK.
  • Openshaw PJM; National Heart and Lung Institute, Imperial College London, London, UK.
  • Drayson MT; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, West Midlands, UK.
  • Shields AM; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, West Midlands, UK.
  • Cunningham AF; Department of Clinical Immunology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Wraith DC; Institute of Microbiology and Infection, University of Birmingham, Birmingham, UK.
  • Richter AG; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, West Midlands, UK.
Clin Exp Immunol ; 213(2): 243-251, 2023 07 21.
Article in En | MEDLINE | ID: mdl-37095599
ABSTRACT
Post-acute cardiac sequelae, following SARS-CoV-2 infection, are well recognized as complications of COVID-19. We have previously shown the persistence of autoantibodies against antigens in skin, muscle, and heart in individuals following severe COVID-19; the most common staining on skin tissue displayed an inter-cellular cement pattern consistent with antibodies against desmosomal proteins. Desmosomes play a critical role in maintaining the structural integrity of tissues. For this reason, we analyzed desmosomal protein levels and the presence of anti-desmoglein (DSG) 1, 2, and 3 antibodies in acute and convalescent sera from patients with COVID-19 of differing clinical severity. We find increased levels of DSG2 protein in sera from acute COVID-19 patients. Furthermore, we find that DSG2 autoantibody levels are increased significantly in convalescent sera following severe COVID-19 but not in hospitalized patients recovering from influenza infection or healthy controls. Levels of autoantibody in sera from patients with severe COVID-19 were comparable to levels in patients with non-COVID-19-associated cardiac disease, potentially identifying DSG2 autoantibodies as a novel biomarker for cardiac damage. To determine if there was any association between severe COVID-19 and DSG2, we stained post-mortem cardiac tissue from patients who died from COVID-19 infection. This confirmed DSG2 protein within the intercalated discs and disruption of the intercalated disc between cardiomyocytes in patients who died from COVID-19. Our results reveal the potential for DSG2 protein and autoimmunity to DSG2 to contribute to unexpected pathologies associated with COVID-19 infection.
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Full text: 1 Database: MEDLINE Main subject: Autoantibodies / COVID-19 Type of study: Diagnostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Clin Exp Immunol Year: 2023 Type: Article Affiliation country: United kingdom

Full text: 1 Database: MEDLINE Main subject: Autoantibodies / COVID-19 Type of study: Diagnostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Clin Exp Immunol Year: 2023 Type: Article Affiliation country: United kingdom