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IgM autoantibodies recognizing ACE2 are associated with severe COVID-19.
Casciola-Rosen, Livia; Thiemann, David R; Andrade, Felipe; Trejo Zambrano, Maria Isabel; Hooper, Jody E; Leonard, Elissa K; Spangler, Jamie B; Cox, Andrea L; Machamer, Carolyn E; Sauer, Lauren; Laeyendecker, Oliver; Garibaldi, Brian T; Ray, Stuart C; Mecoli, Christopher A; Christopher-Stine, Lisa; Gutierrez-Alamillo, Laura; Yang, Qingyuan; Hines, David; Clarke, William A; Rothman, Richard; Pekosz, Andrew; Fenstermacher, Katherine J; Wang, Zitong; Zeger, Scott L; Rosen, Antony.
Afiliación
  • Casciola-Rosen L; Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Thiemann DR; Department of Medicine, Divisioin of Cardiology, Jhohns Hopkins University School of Medicine, Baltimore, Maryland.
  • Andrade F; Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Trejo Zambrano MI; Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Hooper JE; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Leonard EK; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Spangler JB; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Cox AL; Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland.
  • Machamer CE; Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Sauer L; Department of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Laeyendecker O; Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Garibaldi BT; Johns Hopkins Hospital, Adult Emergency Department, Baltimore, Maryland.
  • Ray SC; Division of Intramural Medicine, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Baltimore, Maryland.
  • Mecoli CA; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Christopher-Stine L; Johns Hopkins Biocontainment Unit, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Gutierrez-Alamillo L; Department of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Yang Q; Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Hines D; Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Clarke WA; Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Rothman R; Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Pekosz A; Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Fenstermacher KJ; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Wang Z; Johns Hopkins Hospital, Adult Emergency Department, Baltimore, Maryland.
  • Zeger SL; Department of Environmental Health and Engineering, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.
  • Rosen A; Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.
medRxiv ; 2020 Oct 15.
Article en En | MEDLINE | ID: mdl-33083808
ABSTRACT
SARS-CoV-2 infection induces severe disease in a subpopulation of patients, but the underlying mechanisms remain unclear. We demonstrate robust IgM autoantibodies that recognize angiotensin converting enzyme-2 (ACE2) in 18/66 (27%) patients with severe COVID-19, which are rare (2/52; 3.8%) in hospitalized patients who are not ventilated. The antibodies do not undergo class-switching to IgG, suggesting a T-independent antibody response. Purified IgM from anti-ACE2 patients activates complement. Pathological analysis of lung obtained at autopsy shows endothelial cell staining for IgM in blood vessels in some patients. We propose that vascular endothelial ACE2 expression focuses the pathogenic effects of these autoantibodies on blood vessels, and contributes to the angiocentric pathology observed in some severe COVID-19 patients. These findings may have predictive and therapeutic implications.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: MedRxiv Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: MedRxiv Año: 2020 Tipo del documento: Article
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