6 research outputs found
Early alveolar epithelial cell necrosis is a potential driver of COVID-19-induced acute respiratory distress syndrome
Summary: Acute respiratory distress syndrome (ARDS) with COVID-19 is aggravated by hyperinflammatory responses even after the peak of the viral load has passed; however, its underlying mechanisms remain unclear. In the present study, analysis of the alveolar tissue injury markers and epithelial cell death markers in patients with COVID-19 revealed that COVID-19-induced ARDS was characterized by alveolar epithelial necrosis at an early disease stage. Serum levels of HMGB-1, one of the DAMPs released from necrotic cells, were also significantly elevated in these patients. Further analysis using a mouse model mimicking COVID-19-induced ARDS showed that the alveolar epithelial cell necrosis involved two forms of programmed necrosis, namely necroptosis, and pyroptosis. Finally, the neutralization of HMGB-1 attenuated alveolar tissue injury in the mouse model. Collectively, necrosis, including necroptosis and pyroptosis, is the predominant form of alveolar epithelial cell death at an early disease stage and subsequent release of DAMPs is a potential driver of COVID-19-induced ARDS
Participant timeline.
*Timepoint 1: one day before surgery, Timepoint 2: after obtaining informed consent and till entering the operating room, Timepoint 3: in the operating room before anesthesia induction, Timepoint 4: from trial drug administration to loss of consciousness, Timepoint 5: from loss of consciousness to intubation, Timepoint 6: till 3 minutes after intubation, Timepoint 7: the day after the surgery. Medicines include antihypertensives, sleep inducing drugs, antipsychotics, and central nervous system agents without antidepressants. X indicates the timepoint at which each procedure in the protocol was carried out. Laboratory values include hemoglobin, creatinine, and albumin. AE adverse event, ASA-PS American society of Anesthesiology–physical status, CFS clinical frailty scale, SAE severe adverse event.</p