Impaired Degradation of Neutrophil Extracellular Traps: A Possible Severity Factor of Elderly Male COVID-19 Patients.
de Buhr. Nicole N; Parplys. Ann Christin AC; Schroeder. Maria M; Henneck. Timo T; Schaumburg. Berfin B; Stanelle-Bertram. Stephanie S; Jarczak. Dominik D; Nierhaus. Axel A; Hiller. Jens J; Peine. Sven S; Kluge. Stefan S; Klingel. Karin K; Gabriel. Gülsah G; von Köckritz-Blickwede. Maren M
Key Findings
- COVID‑19 patients, especially males, show elevated NET markers in plasma
- DNase activity is higher in patients overall but declines with age in male patients
- LL‑37 levels rise with NET markers in male patients, suggesting LL‑37 stabilizes NETs and may increase thrombosis risk
Practical Outcomes
- For biohackers, this suggests caution with any LL‑37‑boosting strategies in older men, especially during viral infections. Supporting DNase activity (e.g., through medical use of dornase alfa or lifestyle factors that may enhance endogenous DNase) could help clear NETs. Monitoring inflammation and clot markers may be prudent for high‑risk individuals.
Summary
The study found that older men with COVID‑19 have more sticky DNA webs (NETs) in their blood, partly because a natural peptide called LL‑37 protects these webs from being broken down. While the body’s DNase enzymes that normally clear NETs are higher in COVID patients, they drop off with age in men, making it harder to clear the webs and raising clot risk.
Abstract
Neutrophil extracellular traps (NETs) have been described as a potential trigger of severe COVID-19. NETs are known as extracellular DNA fibers released by neutrophils in response to infection. If the host is unable to balance efficient clearance of NETs by dornases (DNases), detrimental consequences occur. Elevated levels of NETs in COVID-19 patients are associated with higher risk of morbid thrombotic complications. Here, we studied the level of NET markers and DNase activity in a cohort of COVID-19 patients compared to healthy controls. Our data confirmed an increased level of NET markers in the plasma of COVID-19 patients, with a higher level in male compared to female patients. At the same time, there was an increased DNase activity detectable in COVID-19 patients compared to healthy controls. Importantly, there was a negative correlation of DNase activity with the age of male patients. The antimicrobial peptide LL-37, which is known to stabilize NETs against DNase degradation, is embedded in NETs upon severe acute respiratory syndrome coronavirus-2-infection. The LL-37 plasma level correlates with the NET-marker level in male COVID-19 patients, indicating a potential role of LL-37 in the risk of NET-associated thrombosis in male COVID-19 patients by stabilizing NETs against DNase degradation. In conclusion, our data identify two potential risk factors of elderly male patients which may lead to inefficient NET degradation and a subsequently higher risk of NET-associated thrombosis during COVID-19: reduced DNase activity and an increased LL-37 level.
Study Information
pubmed
2022
2022-01-27T00:00:00.000Z
10.1159/000521594
16
49