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Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation
Florence WJ Chioh; Siew-Wai Fong; Barnaby Young; Kan-Xing Wu; Anthony Siau; Shuba Krishnan; Yi-Hao Chan; Louis LY Teo; Fei Gao; Ru San Tan; Liang Zhong; Angela SM Koh; Seow Yen Tan; Paul A Tambyah; Laurent Renia; Lisa F. P. Ng; David Chien Boon Lye; Christine Cheung.
Afiliación
  • Florence WJ Chioh; Nanyang Technological University Singapore, Lee Kong Chian School of Medicine
  • Siew-Wai Fong; Singapore Immunology Network, A*STAR
  • Barnaby Young; National Centre for Infectious Diseases, Singapore
  • Kan-Xing Wu; Nanyang Technological University Singapore, Lee Kong Chian School of Medicine
  • Anthony Siau; Nanyang Technological University Singapore
  • Shuba Krishnan; Karolinska Institute
  • Yi-Hao Chan; Singapore Immunology Network
  • Louis LY Teo; National Heart Centre Singapore
  • Fei Gao; National Heart Centre Singapore
  • Ru San Tan; National Heart Centre Singapore
  • Liang Zhong; National Heart Centre Singapore
  • Angela SM Koh; National Heart Centre Singapore
  • Seow Yen Tan; Changi General Hospital
  • Paul A Tambyah; National University Hospital, Singapore
  • Laurent Renia; A-Star
  • Lisa F. P. Ng; Singapore Immunology Network
  • David Chien Boon Lye; National Centre of Infectious Diseases
  • Christine Cheung; Nanyang Technological University Singapore
Preprint en En | PREPRINT-MEDRXIV | ID: ppmedrxiv-20232835
ABSTRACT
The rapid rise of coronavirus disease 2019 patients who suffer from vascular events after their initial recovery is expected to lead to a worldwide shift in disease burden. We aim to investigate the impact of COVID-19 on the pathophysiological state of blood vessels in convalescent patients. Here, convalescent COVID-19 patients with or without preexisting conditions (i.e. hypertension, diabetes, hyperlipidemia) were compared to non-COVID-19 patients with matched cardiovascular risk factors or healthy participants. Convalescent patients had elevated circulating endothelial cells (CECs), and those with underlying cardiovascular risk had more pronounced endothelial activation hallmarks (ICAM1, P-selectin or CX3CL1) expressed by CECs. Multiplex microbead-based immunoassays revealed some levels of cytokine production sustained from acute infection to recovery phase. Several proinflammatory and activated T lymphocyte-associated cytokines correlated positively with CEC measures, implicating cytokine-driven endothelial dysfunction. Finally, the activation markers detected on CECs mapped to the counter receptors (i.e. ITGAL, SELPLG, and CX3CR1) found primarily on CD8+ T cells and natural killer cells, suggesting that activated endothelial cells could be targeted by cytotoxic effector cells. Clinical trials in preventive therapy for post-COVID-19 vascular complications may be needed. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=69 SRC="FIGDIR/small/20232835v1_ufig1.gif" ALT="Figure 1"> View larger version (19K) org.highwire.dtl.DTLVardef@d34a61org.highwire.dtl.DTLVardef@1b82feeorg.highwire.dtl.DTLVardef@152ea88org.highwire.dtl.DTLVardef@a3b382_HPS_FORMAT_FIGEXP M_FIG C_FIG
Licencia
cc_by_nc_nd
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Prognostic_studies Idioma: En Año: 2020 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Prognostic_studies Idioma: En Año: 2020 Tipo del documento: Preprint