Neutrophil extracellular traps contribute to immunothrombosis in COVID-19 acute respiratory distress syndrome

2020 Blood 1,458 citations

Abstract

Abstract COVID-19 affects millions of patients worldwide, with clinical presentation ranging from isolated thrombosis to acute respiratory distress syndrome (ARDS) requiring ventilator support. Neutrophil extracellular traps (NETs) originate from decondensed chromatin released to immobilize pathogens, and they can trigger immunothrombosis. We studied the connection between NETs and COVID-19 severity and progression. We conducted a prospective cohort study of COVID-19 patients (n = 33) and age- and sex-matched controls (n = 17). We measured plasma myeloperoxidase (MPO)-DNA complexes (NETs), platelet factor 4, RANTES, and selected cytokines. Three COVID-19 lung autopsies were examined for NETs and platelet involvement. We assessed NET formation ex vivo in COVID-19 neutrophils and in healthy neutrophils incubated with COVID-19 plasma. We also tested the ability of neonatal NET-inhibitory factor (nNIF) to block NET formation induced by COVID-19 plasma. Plasma MPO-DNA complexes increased in COVID-19, with intubation (P < .0001) and death (P < .0005) as outcome. Illness severity correlated directly with plasma MPO-DNA complexes (P = .0360), whereas Pao2/fraction of inspired oxygen correlated inversely (P = .0340). Soluble and cellular factors triggering NETs were significantly increased in COVID-19, and pulmonary autopsies confirmed NET-containing microthrombi with neutrophil-platelet infiltration. Finally, COVID-19 neutrophils ex vivo displayed excessive NETs at baseline, and COVID-19 plasma triggered NET formation, which was blocked by nNIF. Thus, NETs triggering immunothrombosis may, in part, explain the prothrombotic clinical presentations in COVID-19, and NETs may represent targets for therapeutic intervention.

Keywords

Neutrophil extracellular trapsARDSImmunologyMedicineRespiratory distressPlatelet activationEx vivoPlateletLungInternal medicineIn vivoBiologyInflammationAnesthesia

MeSH Terms

AdultAgedBetacoronavirusBlood PlateletsBlood ProteinsCOVID-19Coronavirus InfectionsExtracellular TrapsFemaleHumansMaleMiddle AgedNeutrophil InfiltrationNeutrophilsPandemicsPeroxidasePneumoniaViralProspective StudiesSARS-CoV-2Thrombosis

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Publication Info

Year
2020
Type
article
Volume
136
Issue
10
Pages
1169-1179
Citations
1458
Access
Closed

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Social media, news, blog, policy document mentions

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1458
OpenAlex
56
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1267
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Cite This

Elizabeth A. Middleton, Xue‐Yan He, Frederik Denorme et al. (2020). Neutrophil extracellular traps contribute to immunothrombosis in COVID-19 acute respiratory distress syndrome. Blood , 136 (10) , 1169-1179. https://doi.org/10.1182/blood.2020007008

Identifiers

DOI
10.1182/blood.2020007008
PMID
32597954
PMCID
PMC7472714

Data Quality

Data completeness: 86%