| Literature DB >> 33507309 |
Werner J D Ouwendijk1, Matthijs P Raadsen1, Jeroen J A van Kampen1, Robert M Verdijk2, Jan H von der Thusen2, Lihui Guo3,4, Rogier A S Hoek5, Johannes P C van den Akker6, Henrik Endeman6, Thomas Langerak1, Richard Molenkamp1, Diederik Gommers6, Marion P G Koopmans1, Eric C M van Gorp1, Georges M G M Verjans1, Bart L Haagmans1.
Abstract
Lower respiratory tract (LRT) disease induced by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can deteriorate to acute respiratory distress syndrome (ARDS). Because the release of neutrophil extracellular traps (NETs) is implicated in ARDS pathogenesis, we investigated the presence of NETs and correlates of pathogenesis in blood and LRT samples of critically ill patients with COVID-19. Plasma NET levels peaked early after intensive care unit admission and were correlated with the SARS-CoV-2 RNA load in sputum and levels of neutrophil-recruiting chemokines and inflammatory markers in plasma samples. The baseline plasma NET quantity was correlated with disease severity but was not associated with soluble markers of thrombosis or with development of thrombosis. High NET levels were present in LRT samples and persisted during the course of COVID-19, consistent with the detection of NETs in bronchi and alveolar spaces in lung tissue from deceased patient with COVID-19. Thus, NETs are produced and retained in the LRT of critically ill patients with COVID-19 and could contribute to SARS-CoV-2-induced ARDS disease.Entities:
Keywords: COVID-19; SARS-CoV-2; acute respiratory distress syndrome; neutrophil extracellular traps; neutrophils
Year: 2021 PMID: 33507309 PMCID: PMC7928833 DOI: 10.1093/infdis/jiab050
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226