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Adverse Outcome in COVID-19 Is Associated With an Aggravating Hypo-Responsive Platelet Phenotype
Waltraud C Schrottmaier1, Anita Pirabe1, David Pereyra1,2
1Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Insights
COVID-19 patients with severe outcomes show hypo-responsive platelets, impacting immune responses. This platelet dysfunction worsens during hospitalization, suggesting a link between platelet function and disease severity.
Area of Science:
- Hematology
- Immunology
- Infectious Diseases
Background:
- Thromboembolic events are common in Coronavirus disease 2019 (COVID-19).
- COVID-19 is associated with platelet dysregulation, but its impact on disease outcome remains unclear.
- Understanding platelet function in COVID-19 is crucial for predicting disease severity.
Purpose of the Study:
- To investigate platelet activation and reactivity in hospitalized COVID-19 patients.
- To determine the association between platelet function and adverse COVID-19 outcomes.
- To explore the role of plasma components in COVID-19-associated platelet dysfunction.
Main Methods:
- Prospective monitoring of platelet activation and reactivity in 97 hospitalized COVID-19 patients during the first week.
- Measurement of plasma markers for platelet degranulation and inflammation.
- Assessment of platelet aggregation and platelet-leukocyte aggregate formation.
Main Results:
- Adverse COVID-19 outcomes correlated with increased basal platelet activation and reduced platelet responses, worsening over time.
- Diminished GPIIb/IIIa responses indicated impaired platelet aggregation.
- Reduced platelet-leukocyte aggregate formation suggested compromised platelet-mediated immune responses.
- No evidence of platelet exhaustion was found; plasma from severe COVID-19 patients impaired platelet function in healthy donors.
Conclusions:
- Unfavorable COVID-19 outcomes are linked to a progressive hypo-responsive platelet phenotype.
- This platelet dysfunction may impair platelet-mediated immunoregulation.
- Plasma factors in severe COVID-19 contribute to platelet hypo-responsiveness.
Abstract:
Thromboembolic complications are frequently observed in Coronavirus disease 2019 (COVID-19). While COVID-19 is linked to platelet dysregulation, the association between disease outcome and platelet function is less clear. We prospectively monitored platelet activation and reactivity in 97 patients during the first week of hospitalization and determined plasma markers of platelet degranulation and inflammation. Adverse outcome in COVID-19 was associated with increased basal platelet activation and diminished platelet responses, which aggravated over time. Especially GPIIb/IIIa responses were abrogated, pointing toward impeded platelet aggregation. Moreover, platelet-leukocyte aggregate formation was diminished, pointing toward abrogated platelet-mediated immune responses in COVID-19. No general increase in plasma levels of platelet-derived granule components could be detected, arguing against platelet exhaustion. However, studies on platelets from healthy donors showed that plasma components in COVID-19 patients with unfavorable outcome were at least partly responsible for diminished platelet responses. Taken together this study shows that unfavorable outcome in COVID-19 is associated with a hypo-responsive platelet phenotype that aggravates with disease progression and may impact platelet-mediated immunoregulation.
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