Patients with COVID-19: in the dark-NETs of neutrophils.
Patients with COVID-19: in the dark-NETs of neutrophils.
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DOI:
10.1038/s41418-021-00805-z
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发表时间:
2021-11
影响因子:
12.4
通讯作者:
Herrmann M
中科院分区:
文献类型:
--
作者:
Ackermann M;Anders HJ;Bilyy R;Bowlin GL;Daniel C;De Lorenzo R;Egeblad M;Henneck T;Hidalgo A;Hoffmann M;Hohberger B;Kanthi Y;Kaplan MJ;Knight JS;Knopf J;Kolaczkowska E;Kubes P;Leppkes M;Mahajan A;Manfredi AA;Maueröder C;Maugeri N;Mitroulis I;Muñoz LE;Narasaraju T;Naschberger E;Neeli I;Ng LG;Radic MZ;Ritis K;Rovere-Querini P;Schapher M;Schauer C;Simon HU;Singh J;Skendros P;Stark K;Stürzl M;van der Vlag J;Vandenabeele P;Vitkov L;von Köckritz-Blickwede M;Yanginlar C;Yousefi S;Zarbock A;Schett G;Herrmann M
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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DOI:
10.1074/jbc.m110.103275
发表时间:
2010-07-23
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Belouzard S;Madu I;Whittaker GR
通讯作者:
Whittaker GR
影响因子:
24.8
作者:
Carmona-Rivera, Carmelo;Carlucci, Philip M.;Kaplan, Mariana J.
通讯作者:
Kaplan, Mariana J.
影响因子:
158.5
作者:
Boulware, David R.;Pullen, Matthew F.;Hullsiek, Kathy H.
通讯作者:
Hullsiek, Kathy H.
影响因子:
16.6
作者:
Ali, Ramadan A.;Gandhi, Alex A.;Knight, Jason S.
通讯作者:
Knight, Jason S.
影响因子:
32.4
作者:
Adrover, Jose M.;del Fresno, Carlos;Hidalgo, Andres
通讯作者:
Hidalgo, Andres