Patients with COVID-19: in the dark-NETs of neutrophils

Maximilian Ackermann(Johannes Gutenberg University Mainz), Hans‐Joachim Anders(LMU Klinikum), Rostyslav Bilyy(Danylo Halytsky Lviv National Medical University), Gary L. Bowlin(University of Memphis), Christoph Daniel(Friedrich-Alexander-Universität Erlangen-Nürnberg), Rebecca De Lorenzo(Vita-Salute San Raffaele University), Mikala Egeblad(Cold Spring Harbor Laboratory), Timo Henneck(University of Veterinary Medicine Hannover, Foundation), Andrés Hidalgo(Spanish National Centre for Cardiovascular Research), Markus Hoffmann(Friedrich-Alexander-Universität Erlangen-Nürnberg), Bettina Hohberger(Friedrich-Alexander-Universität Erlangen-Nürnberg), Yogendra Kanthi(University of Michigan), Mariana J. Kaplan(National Institutes of Health), Jason S. Knight(University of Michigan), Jasmin Knopf(Friedrich-Alexander-Universität Erlangen-Nürnberg), Elżbieta Kołaczkowska(Jagiellonian University), Paul Kubes(University of Calgary), Moritz Leppkes(Friedrich-Alexander-Universität Erlangen-Nürnberg), Aparna Mahajan(Friedrich-Alexander-Universität Erlangen-Nürnberg), Angelo A. Manfredi(Vita-Salute San Raffaele University), Christian Maueröder(Ghent University), Norma Maugeri(Vita-Salute San Raffaele University), Ioannis Mitroulis(Democritus University of Thrace), Luis E. Muñoz(Friedrich-Alexander-Universität Erlangen-Nürnberg), Teluguakula Narasaraju(Oklahoma State University Center for Health Sciences), Elisabeth Naschberger(Friedrich-Alexander-Universität Erlangen-Nürnberg), Indira Neeli(University of Tennessee Health Science Center), Lai Guan Ng(Singapore Immunology Network), Marko Radic(University of Tennessee Health Science Center), Konstantinos Ritis(Democritus University of Thrace), Patrizia Rovere‐Querini(Vita-Salute San Raffaele University), Mirco Schapher(Friedrich-Alexander-Universität Erlangen-Nürnberg), Christine Schauer(Friedrich-Alexander-Universität Erlangen-Nürnberg), Hans‐Uwe Simon(University of Bern), Jeeshan Singh(Friedrich-Alexander-Universität Erlangen-Nürnberg), Panagiotis Skendros(Democritus University of Thrace), Konstantin Stark(Ludwig-Maximilians-Universität München), Michael Stürzl(Friedrich-Alexander-Universität Erlangen-Nürnberg), Johan van der Vlag(Radboud University Nijmegen), Peter Vandenabeele(Ghent University), Ljubomir Vitkov(University of Salzburg), Maren von Köckritz‐Blickwede(University of Veterinary Medicine Hannover, Foundation), Cansu Yanginlar(Radboud University Nijmegen), Shída Yousefi(University of Bern), Alexander Zarbock(University Hospital Münster), Georg Schett(Friedrich-Alexander-Universität Erlangen-Nürnberg), Martin Herrmann(Friedrich-Alexander-Universität Erlangen-Nürnberg)
Cell Death and Differentiation
May 24, 2021
Cited by 318Open Access
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Abstract

SARS-CoV-2 infection poses a major threat to the lungs and multiple other organs, occasionally causing death. Until effective vaccines are developed to curb the pandemic, it is paramount to define the mechanisms and develop protective therapies to prevent organ dysfunction in patients with COVID-19. Individuals that develop severe manifestations have signs of dysregulated innate and adaptive immune responses. Emerging evidence implicates neutrophils and the disbalance between neutrophil extracellular trap (NET) formation and degradation plays a central role in the pathophysiology of inflammation, coagulopathy, organ damage, and immunothrombosis that characterize severe cases of COVID-19. Here, we discuss the evidence supporting a role for NETs in COVID-19 manifestations and present putative mechanisms, by which NETs promote tissue injury and immunothrombosis. We present therapeutic strategies, which have been successful in the treatment of immunο-inflammatory disorders and which target dysregulated NET formation or degradation, as potential approaches that may benefit patients with severe COVID-19.


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