Antibodies (May 2024)

Antibodies against Platelet Glycoproteins in Clinically Suspected VITT Patients

  • Romy T. Meier,
  • Leendert Porcelijn,
  • Suzanne Hofstede-van Egmond,
  • Camila Caram-Deelder,
  • Jonathan M. Coutinho,
  • Yvonne M. C. Henskens,
  • Marieke J. H. A. Kruip,
  • An K. Stroobants,
  • Jaap J. Zwaginga,
  • C. Ellen van der Schoot,
  • Masja de Haas,
  • Rick Kapur

DOI
https://doi.org/10.3390/antib13020035
Journal volume & issue
Vol. 13, no. 2
p. 35

Abstract

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Vaccine-induced thrombotic thrombocytopenia (VITT) is a rare but severe complication following COVID-19 vaccination, marked by thrombocytopenia and thrombosis. Analogous to heparin-induced thrombocytopenia (HIT), VITT shares similarities in anti-platelet factor 4 (PF4) IgG-mediated platelet activation via the FcγRIIa. To investigate the involvement of platelet-antibodies in VITT, we analyzed the presence of platelet-antibodies directed against glycoproteins (GP)IIb/IIIa, GPV and GPIb/IX in the serum of 232 clinically suspected VITT patients determined based on (suspicion of) occurrence of thrombocytopenia and/or thrombosis in relation to COVID-19 vaccination. We found that 19% of clinically suspected VITT patients tested positive for anti-platelet GPs: 39%, 32% and 86% patients tested positive for GPIIb/IIIa, GPV and GPIb/IX, respectively. No HIT-like VITT patients (with thrombocytopenia and thrombosis) tested positive for platelet-antibodies. Therefore, it seems unlikely that platelet-antibodies play a role in HIT-like anti-PF4-mediated VITT. Platelet-antibodies were predominantly associated with the occurrence of thrombocytopenia. We found no association between the type of vaccination (adenoviral vector vaccine versus mRNA vaccine) or different vaccines (ChAdOx1 nCoV-19, Ad26.COV2.S, mRNA-1273, BTN162b2) and the development of platelet-antibodies. It is essential to conduct more research on the pathophysiology of VITT, to improve diagnostic approaches and identify preventive and therapeutic strategies.

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