Role of Microvesicles and Netosis in Coagulopathy in Patients With SARS-CoV-2 Infection: A Randomized Clinical Trial
- Authors: Gracheva E.S.1, Mustafin I.G.1, Samigullin D.V.2,3, Abdulganieva D.I.1
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Affiliations:
- Kazan State Medical University
- Kazan Institute of Biochemistry and Biophysics — Kazan Scientific Center of Russian Academy of Sciences
- Kazan National Research Technical University named after A.N. Tupolev-KAI
- Section: Original research
- Submitted: 26.06.2025
- Accepted: 11.08.2025
- Published: 24.09.2025
- URL: https://kazanmedjournal.ru/kazanmedj/article/view/685965
- DOI: https://doi.org/10.17816/KMJ685965
- EDN: https://elibrary.ru/KLXJZX
- ID: 685965
Cite item
Abstract
BACKGROUND: The high incidence of thrombotic complications in patients with SARS-CoV-2 infection significantly worsens the prognosis of the disease. The primary issue is limited comprehension on the mechanisms by which systemic inflammation, neutrophil activation, extracellular neutrophil traps, and microvesicle-mediated hemostasis disorders are interconnected.
AIM: This study aimed to investigate the link between microvesicles and extracellular neutrophil traps and the occurrence of coagulopathies in patients with SARS-CoV-2 infection. The quantitative and qualitative characteristics of these phenomena were assessed based on the severity of the patients’ condition.
METHODS: The study included 213 patients with SARS-CoV-2 infection (138 patients with moderate disease and 75 with severe disease) and 20 healthy donors. The patients underwent blood chemistry, coagulation, and hematology tests. A quantitative analysis of microvesicles was performed using flow cytometry with monoclonal antibodies specific for surface markers (CD45, CD3, CD14, CD15, and CD61). The interaction of microvesicles with extracellular neutrophil traps was observed by confocal microscopy (Leica TCS SP5) using fluorescent labels (DAPI, FITC, APC, and PE) and subsequently analyzed for colocalization using a LAS AF package. Statistical analysis was conducted using the Student’s t-test, Spearman’s correlation coefficient, and linear regression methods.
RESULTS: The patients with moderate SARS-CoV-2 infection had hypercoagulation (fibrinogen, 4.8 [4.00; 5.60] g/L; D-dimer, 0.78 [0.30; 1.28] mg/L), with increased levels of neutrophil-derived (CD15⁺, 53.34% ± 6.92%) and platelet-derived (CD61⁺, 59.74% ± 11.22%) microvesicles. Tissue factor-enriched filamentous extracellular neutrophil traps with microvesicles were identified. The severe cases were associated with decreased levels of neutrophil-derived (CD15⁺, 10.32% ± 4.29%) and platelet-derived (CD61⁺, 20.9% ± 6.01%) microvesicles, thrombocytopenia (139.5 [104.25; 177.75] × 10⁹/L), hypocoagulation (international normalized ratio: 2.60 [2.32; 3.58]), and CD62⁺-positive aggregates.
CONCLUSION: Microvesicles and extracellular neutrophil traps play a key role in dysregulated hemostasis in patients with SARS-CoV-2 infection. Early hypercoagulation is mediated by their procoagulant activity, and severe cases are associated with decreased levels of peripheral microvesicles, which is indicative of consumptive coagulopathy.
About the authors
Elena S. Gracheva
Kazan State Medical University
Author for correspondence.
Email: Gracheva020688@mail.ru
ORCID iD: 0000-0002-8543-6529
SPIN-code: 3290-5459
Postgrad. Student, Assistant, Depart. of Biochemistry and Clinical Laboratory Diagnostics
Russian Federation, KazanIl’shat G. Mustafin
Kazan State Medical University
Email: ilshat.mustafin@kazangmu.ru
ORCID iD: 0000-0001-9683-3012
SPIN-code: 1588-6988
Scopus Author ID: 6602360648
MD, Dr. Sci. (Medicine), Professor, Head, Depart. of Biochemistry and Clinical Laboratory Diagnostics
Russian Federation, KazanDmitry V. Samigullin
Kazan Institute of Biochemistry and Biophysics — Kazan Scientific Center of Russian Academy of Sciences; Kazan National Research Technical University named after A.N. Tupolev-KAI
Email: samid75@mail.ru
ORCID iD: 0000-0001-6019-5514
SPIN-code: 4751-7443
Cand. Sci. (biology), Head, Lab. of Biophysics and Synaptic Processes
Russian Federation, Kazan; KazanDiana I. Abdulganieva
Kazan State Medical University
Email: diana-s@mail.ru
ORCID iD: 0000-0001-7069-2725
SPIN-code: 6676-4270
Scopus Author ID: 39161040600
MD, Dr. Sci. (Medicine), Professor, Head, Hospital therapy depart.
Russian Federation, KazanReferences
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