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Enhancement of NETosis by ACE2-cross-reactive anti-SARS-CoV-2 RBD antibodies in patients with COVID-19.
Hsieh, Kun-Han; Chao, Chiao-Hsuan; Cheng, Yi-Ling; Lai, Yen-Chung; Chuang, Yung-Chun; Wang, Jen-Ren; Chang, Sui-Yuan; Hung, Yuan-Pin; Chen, Yi-Ming Arthur; Liu, Wei-Lun; Chuang, Woei-Jer; Yeh, Trai-Ming.
Afiliação
  • Hsieh KH; Department of Medical Laboratory Science and Biotechnology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Chao CH; Department of Medical Laboratory Science and Biotechnology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Cheng YL; Department of Medical Laboratory and Regenerative Medicine, MacKay Medical College, New Taipei, Taiwan.
  • Lai YC; Department of Medical Laboratory Science and Biotechnology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Chuang YC; Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, 92037, USA.
  • Wang JR; Division of Infectious Diseases, Department of Medicine, University of California, San Diego, La Jolla, CA, 92037, USA.
  • Chang SY; Department of Medical Laboratory Science and Biotechnology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Hung YP; Leadgene Biomedical, Inc, Tainan, Taiwan.
  • Chen YA; Department of Biomedical Sciences, Chung Shan Medical University, Taichung, Taiwan.
  • Liu WL; Department of Medical Laboratory Science and Biotechnology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Chuang WJ; Diseases and Vaccinology, National Institute of Infectious National Health Research Institutes, Tainan, Taiwan.
  • Yeh TM; Center of Infectious Disease and Signaling Research, National Cheng Kung University, Tainan, Taiwan.
J Biomed Sci ; 31(1): 39, 2024 Apr 18.
Article em En | MEDLINE | ID: mdl-38637878
ABSTRACT

BACKGROUND:

High levels of neutrophil extracellular trap (NET) formation or NETosis and autoantibodies are related to poor prognosis and disease severity of COVID-19 patients. Human angiotensin-converting enzyme 2 (ACE2) cross-reactive anti-severe acute respiratory syndrome coronavirus 2 spike protein receptor-binding domain (SARS-CoV-2 RBD) antibodies (CR Abs) have been reported as one of the sources of anti-ACE2 autoantibodies. However, the pathological implications of CR Abs in NET formation remain unknown.

METHODS:

In this study, we first assessed the presence of CR Abs in the sera of COVID-19 patients with different severity by serological analysis. Sera and purified IgG from CR Abs positive COVID-19 patients as well as a mouse monoclonal Ab (mAb 127) that can recognize both ACE2 and the RBD were tested for their influence on NETosis and the possible mechanisms involved were studied.

RESULTS:

An association between CR Abs levels and the severity of COVID-19 in 120 patients was found. The CR Abs-positive sera and IgG from severe COVID-19 patients and mAb 127 significantly activated human leukocytes and triggered NETosis, in the presence of RBD. This NETosis, triggered by the coexistence of CR Abs and RBD, activated thrombus-related cells but was abolished when the interaction between CR Abs and ACE2 or Fc receptors was disrupted. We also revealed that CR Abs-induced NETosis was suppressed in the presence of recombinant ACE2 or the Src family kinase inhibitor, dasatinib. Furthermore, we found that COVID-19 vaccination not only reduced COVID-19 severity but also prevented the production of CR Abs after SARS-CoV-2 infection.

CONCLUSIONS:

Our findings provide possible pathogenic effects of CR Abs in exacerbating COVID-19 by enhancing NETosis, highlighting ACE2 and dasatinib as potential treatments, and supporting the benefit of vaccination in reducing disease severity and CR Abs production in COVID-19 patients.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article