Whole Blood Procoagulant Platelet Flow Cytometry Protocol for Heparin-Induced Thrombocytopenia (HIT) and Vaccine-Induced Immune Thrombotic Thrombocytopenia (VITT) Testing.
Christine Shu Mei LeeMatthew C PowellVivien M Y ChenPublished in: Methods in molecular biology (Clifton, N.J.) (2023)
Heparin-induced thrombocytopenia (HIT) is a well-characterized, iatrogenic complication of heparin anticoagulation with significant morbidity. In contrast, vaccine-induced immune thrombotic thrombocytopenia (VITT) is a recently recognized severe prothrombotic complication of adenoviral vaccines, including the ChAdOx1 nCoV-19 (Vaxzevria, AstraZeneca) and Ad26.COV2.S (Janssen, Johnson & Johnson) vaccines against COVID-19. The diagnosis of HIT and VITT involve laboratory testing for antiplatelet antibodies by immunoassays followed by confirmation by functional assays to detect platelet-activating antibodies. Functional assays are critical to detect pathological antibodies due to the varying sensitivity and specificity of immunoassays. This chapter presents a protocol for a novel whole blood flow cytometry-based assay to detect procoagulant platelets in healthy donor blood in response to plasma from patients suspected of HIT or VITT. A method to identify suitable healthy donors for HIT and VITT testing is also described.
Keyphrases
- flow cytometry
- high glucose
- diabetic rats
- sars cov
- randomized controlled trial
- coronavirus disease
- end stage renal disease
- ejection fraction
- oxidative stress
- pulmonary embolism
- endothelial cells
- prognostic factors
- magnetic resonance imaging
- computed tomography
- atrial fibrillation
- chronic kidney disease
- magnetic resonance
- respiratory syndrome coronavirus
- patient reported outcomes