A flow cytometric assay to detect platelet-activating antibodies in VITT after ChAdOx1 nCov-19 vaccination

Blood. 2021 Jul 1;137(26):3656-3659. doi: 10.1182/blood.2021012064.

Abstract

Vaccination is crucial in combatting the severe acute respiratory syndrome coronavirus 2 pandemic. The rare complication of thrombocytopenia and thrombotic complications at unusual sites after ChAdOx1 nCov-19 vaccination is caused by platelet-activating antibodies directed against platelet factor 4 (PF4). We present a widely applicable whole-blood standard flow cytometric assay to identify the pathogenic antibodies associated with vaccine-induced immune-mediated thrombotic thrombocytopenia (VITT) after ChAdOx1 nCov-19 vaccination. This assay will enable rapid diagnosis by many laboratories. This trial was registered at www.clinicaltrials.gov as #NCT04370119.

Publication types

  • Clinical Trial
  • Research Support, N.I.H., Extramural

MeSH terms

  • Antibody Specificity
  • Autoantibodies / biosynthesis
  • Autoantibodies / blood*
  • Autoantibodies / immunology
  • COVID-19 / prevention & control*
  • COVID-19 Vaccines / adverse effects*
  • COVID-19 Vaccines / immunology
  • ChAdOx1 nCoV-19
  • Flow Cytometry / methods*
  • Heparin / adverse effects
  • Heparin / immunology
  • Humans
  • Immunoenzyme Techniques
  • Immunogenicity, Vaccine
  • Immunoglobulin G / biosynthesis
  • Immunoglobulin G / blood*
  • Immunoglobulin G / immunology
  • P-Selectin / analysis
  • Platelet Activation / immunology*
  • Platelet Factor 4 / immunology*
  • Purpura, Thrombocytopenic, Idiopathic / diagnosis*
  • Purpura, Thrombocytopenic, Idiopathic / etiology
  • Purpura, Thrombocytopenic, Idiopathic / immunology
  • Receptors, IgG / immunology*
  • SARS-CoV-2*
  • Vaccination / adverse effects*

Substances

  • Autoantibodies
  • COVID-19 Vaccines
  • Fc gamma receptor IIA
  • Immunoglobulin G
  • P-Selectin
  • PF4 protein, human
  • Receptors, IgG
  • SELP protein, human
  • Platelet Factor 4
  • Heparin
  • ChAdOx1 nCoV-19

Associated data

  • ClinicalTrials.gov/NCT04370119