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Population-wide persistent hemostatic changes after vaccination with ChAdOx1-S.
Bas de Laat1,2, Hendrik Stragier3,4, Romy de Laat-Kremers2
1Department of Functional Coagulation, Synapse Research Institute, Maastricht, Netherlands.
Frontiers in Cardiovascular Medicine
|August 15, 2022
Summary
ChAdOx1-S vaccination was linked to altered hemostasis in health care workers. The vaccine may increase thrombosis risk through endothelial activation and a procoagulant profile.
Area of Science:
- Hematology
- Immunology
- Vaccinology
Background:
- Reports suggest a potential link between anti-SARS-CoV-2 vaccines, including ChAdOx1-S, and an increased risk of thrombosis.
- Understanding the hemostatic and immune changes post-vaccination is crucial for assessing vaccine safety.
Purpose of the Study:
- To investigate the hemostatic and immune system changes following ChAdOx1-S vaccination.
- To evaluate potential mechanisms linking ChAdOx1-S vaccination to thrombotic events.
Main Methods:
- Blood samples from 631 health care workers were analyzed post-second ChAdOx1-S vaccination.
- Assessed hemostatic markers (D-dimer, fibrinogen, thrombin generation), endothelial function (VWF, active VWF), and immune markers (IL-6, IL-10).
- SARS-CoV-2 antibody titers were also determined.
Main Results:
- Vaccinated subjects showed reduced prothrombin and fibrinogen levels but higher prevalence outside normal ranges for prothrombin and antithrombin.
- Thrombin generation analysis revealed a more procoagulant profile with shortened lag time and time-to-peak, and increased peak height.
- Increased Von Willebrand Factor (VWF) and active VWF indicated endothelial activation, alongside significantly elevated IL-10 levels.
Conclusions:
- ChAdOx1-S vaccination is associated with significant alterations in hemostasis, including a procoagulant profile and endothelial activation.
- Persistently increased IL-10 suggests ongoing immune system activity post-vaccination, potentially contributing to thrombotic risk.
- These findings highlight a possible pathophysiological mechanism for increased thrombotic events after ChAdOx1-S vaccination.
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