John Libbey Eurotext

Hématologie

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Neutrophil extracellular traps: key drivers of severe Covid-19 Volume 27, issue 4, Juillet-Août 2021

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Authors
1 Laboratoire de cardiologie, institut Giga, université de Liège, Liège, Belgique
2 Directrice de recherche au Fonds national de la recherche scientifique (FRS-FNRS), Belgique
3 Laboratoire d’immunophysiologie, institut Giga, université de Liège, Liège, Belgique
4 Faculé de médecine vétérinaire, université de Liège, Liège, Belgique
5 WELBIO, Walloon Excellence in Life Sciences and Biotechnology, Wallonie, Belgique
* Tirés à part

In severe Covid-19, hyperinflammatory tissue-damaging, thromboembolic or immunothrombotic responses triggered by Sars-Cov-2 are major causes of respiratory failure and death. Neutrophil extracellular traps (NETs), released by activated neutrophils during a process called NETosis, can be formed in the lungs upon infection with respiratory viruses. They have the ability to promote lung damage, thrombosis and fibrosis, three cardinal features encountered in severe Covid-19. In a recent study, we sought to understand how NETosis could relate to lung immunopathological changes associated with fatal cases of the disease. We assessed whether NET structures could be identified in post-mortem lung biopsies from Covid-19 patients, and whether they were located in particular lesions and micro-anatomical lung compartments. We performed immunofluorescence staining of myeloperoxidase, citrullinated histone H3 and nuclear acid (DAPI) on sections of paraffin-embedded lung biopsies from four Covid-19 patients who succumbed Covid-19 and from four patients who died from a Covid-19-unrelated cause. The four patients represented prototypical severe and fatal cases of Covid-19, characterized by pneumonia and fatal respiratory distress associated with signs of systemic inflammation, neutrophilia and coagulopathy. NETs were uniquely detected in the lungs of each Covid-19 patient. Detailed histopathological analysis revealed widely distributed NET-infiltrating areas encompassing several lung compartments, including arteriolar microthrombi, neutrophil-rich inflammatory areas of lung interstitium as well as alveoli or bronchioles where they often co-localized with occluding fibrin-rich deposits. Another study published simultaneously to ours provides first experimental evidence for causality between NETosis and lung injury in severe Covid-19. However, the possible involvement of NETs in thrombogenesis remains to be addressed. Notwithstanding, these data support the hypothesis that NETs may represent drivers of Covid-19-associated severe pulmonary complications, and suggest that NET-targeting approaches could represent potential avenues for the treatment of uncontrolled tissue-damaging, thrombotic or fibrotic responses to Sars-Cov-2.