Patients with COVID-19: in the dark-NETs of neutrophils
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Published:2021-05-24
Issue:11
Volume:28
Page:3125-3139
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ISSN:1350-9047
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Container-title:Cell Death & Differentiation
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language:en
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Short-container-title:Cell Death Differ
Author:
Ackermann Maximilian, Anders Hans-Joachim, Bilyy RostyslavORCID, Bowlin Gary L., Daniel Christoph, De Lorenzo Rebecca, Egeblad Mikala, Henneck Timo, Hidalgo Andrés, Hoffmann MarkusORCID, Hohberger Bettina, Kanthi Yogendra, Kaplan Mariana J.ORCID, Knight Jason S., Knopf Jasmin, Kolaczkowska Elzbieta, Kubes Paul, Leppkes Moritz, Mahajan Aparna, Manfredi Angelo A., Maueröder Christian, Maugeri NormaORCID, Mitroulis Ioannis, Muñoz Luis E.ORCID, Narasaraju Teluguakula, Naschberger Elisabeth, Neeli Indira, Ng Lai Guan, Radic Marko Z.ORCID, Ritis Konstantinos, Rovere-Querini Patrizia, Schapher Mirco, Schauer Christine, Simon Hans-Uwe, Singh Jeeshan, Skendros Panagiotis, Stark Konstantin, Stürzl MichaelORCID, van der Vlag JohanORCID, Vandenabeele PeterORCID, Vitkov LjubomirORCID, von Köckritz-Blickwede MarenORCID, Yanginlar Cansu, Yousefi ShidaORCID, Zarbock Alexander, Schett GeorgORCID, Herrmann MartinORCID
Abstract
AbstractSARS-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.
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology
Reference182 articles.
1. Cowland JB, Borregaard N. Granulopoiesis and granules of human neutrophils. Immunol Rev. 2016;273:11–28. 2. Rubio-Ponce A, Hidalgo A, Ballesteros I. How to bridle a neutrophil. Curr Opin Immunol. 2021;68:41–47. 3. Hidalgo A, Chilvers ER, Summers C, Koenderman L. The neutrophil life cycle. Trends Immunol. 2019;40:584–97. 4. Casanova-Acebes M, Pitaval C, Weiss LA, Nombela-Arrieta C, Chevre R, AG N, et al. Rhythmic modulation of the hematopoietic niche through neutrophil clearance. Cell. 2013;153:1025–35. 5. Adrover JM, Aroca-Crevillen A, Crainiciuc G, Ostos F, Rojas-Vega Y, Rubio-Ponce A, et al. Programmed ‘disarming’ of the neutrophil proteome reduces the magnitude of inflammation. Nat Immunol. 2020;21:135–44.
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