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10.4049/jimmunol.2200021

http://scihub22266oqcxt.onion/10.4049/jimmunol.2200021
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35896335!ä!35896335

suck abstract from ncbi


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pmid35896335      J+Immunol 2022 ; 209 (4): 655-659
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  • Cutting Edge: Hyperinflammatory Monocytes Expressing CD56 Abound in Severe COVID-19 Patients #MMPMID35896335
  • Campana S; De Pasquale C; Sidoti Migliore G; Pezzino G; Cavaliere R; Venanzi Rullo E; Nunnari G; Caramori G; David A; Bonaccorsi I; Pollicino T; Carrega P; Ferlazzo G
  • J Immunol 2022[Aug]; 209 (4): 655-659 PMID35896335show ga
  • Proinflammatory monocytes play a preponderant role in the development of a cytokine storm causing fatal consequences in coronavirus disease 2019 (COVID-19) patients, highlighting the importance of analyzing in more detail monocyte distribution in these patients. In this study, we identified an atypical monocyte subpopulation expressing CD56 molecules that showed a low level of HLA-DR and high level of l-selectin. They released higher amounts of TNF-alpha and IL-6 and expressed genes associated with an excessive inflammatory process. Remarkably, the frequency of CD56(+) monocytes inversely correlated with that of CD16(+) monocytes and a high CD56(+)/CD16(+)monocyte ratio was associated with both disease severity and mortality, as well as with serum concentration of type I IFN, a factor able to induce the appearance of CD56(+) monocytes. In conclusion, severe COVID-19 is characterized by the abundance of hyperinflammatory CD56(+) monocytes, which could represent a novel marker with prognostic significance and, possibly, a therapeutic target for controlling the inflammatory process occurring during COVID-19.
  • |*COVID-19[MESH]
  • |*Monocytes[MESH]
  • |Cytokine Release Syndrome[MESH]
  • |HLA-DR Antigens[MESH]
  • |Humans[MESH]
  • |Receptors, IgG/genetics[MESH]


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