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10.1016/j.ijid.2021.05.001

http://scihub22266oqcxt.onion/10.1016/j.ijid.2021.05.001
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33965598!8119437!33965598
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suck abstract from ncbi


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pmid33965598      Int+J+Infect+Dis 2021 ; 107 (ä): 232-233
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  • Potential value of circulating endothelial cells for the diagnosis and treatment of COVID-19 #MMPMID33965598
  • Zhang X; Jiang M; Yang J
  • Int J Infect Dis 2021[Jun]; 107 (ä): 232-233 PMID33965598show ga
  • The ongoing severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic has been a formidable global challenge. As yet, there are very few drugs to treat this infection and no vaccine is currently available. It has gradually become apparant that coronavirus disease 2019 (COVID-19) is not a simple disease involving a single organ; rather, many vital organs and systems are affected. The endothelium is one target of SARS-CoV-2. Damaged endothelial cells, which break away from organs and enter the bloodstream to form circulating endothelial cells, were recently reported as putative biomarkers for COVID-19. Modulation of the expression level of sphingosine-1 phosphate via sphingosine kinase activation can control endothelial cell proliferation and apoptosis. As such, it may be possible to obtain a sensitive and specific diagnosis of the severity of COVID-19 by assessing the absolute number and the viable/apoptotic ratio of circulating endothelial cells. Furthermore, a focus on the endothelium could help to develop a strategy for COVID-19 treatment from the perspective of endothelial protection and repair.
  • |*SARS-CoV-2[MESH]
  • |Biomarkers[MESH]
  • |COVID-19/*diagnosis/therapy[MESH]
  • |Cystic Fibrosis Transmembrane Conductance Regulator/physiology[MESH]
  • |Endothelial Cells/*pathology[MESH]
  • |Humans[MESH]
  • |Lysophospholipids/analysis[MESH]


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