Frontiers in Immunology (Dec 2024)

Interpreting high levels of unfolded Von Willebrand Factor in patients with the antiphospholipid syndrome

  • Romy de Laat-Kremers,
  • Shengshi Huang,
  • Shengshi Huang,
  • Hugo ten Cate,
  • Hugo ten Cate,
  • Marisa Ninivaggi,
  • Bas de Laat,
  • Bas de Laat,
  • Katrien Devreese,
  • Katrien Devreese

DOI
https://doi.org/10.3389/fimmu.2024.1514433
Journal volume & issue
Vol. 15

Abstract

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IntroductionUnfolded Von Willebrand Factor (VWF) is increased in thrombotic pathologies such as myocardial infarction. Unfolded VWF mediates the binding of platelets without the need for collagen. β2-glycoprotein I (β2-GPI) is a natural inhibitor of the platelet-VWF interaction. The antiphospholipid syndrome (APS) is associated with thrombosis, with an important pathophysiological role of auto-antibodies directed against β2-GPI.Methods(Unfolded) VWF levels were studied in normal controls (n=93), APS patients (n=64), non-APS thrombosis patients (n=39) and non-APS auto-immune disease (AID) patients (n=49.ResultsUnfolded VWF levels were respectively, 53%, 50% and 36% higher in APS patients, non-APS thrombosis patients and AID patients, compared to normal controls (p<0.0001). Unfolded VWF levels above the 90th percentile in normal controls were associated with an odds of APS (OR: 8.51; CI:3.26 - 22.2; p<0.001), compared to ORs of non-APS thrombosis (OR:5.87; CI:2.07 - 16.7, p=0.001) and AID (OR:3.71; CI:1.40 – 9.87; p=0.009). DiscussionWe found that APS patients have high levels of unfolded VWF in their circulation. In APS, auto-antibodies against-β2-GPI may interfere with the β2-GPI-mediated inhibition of VWF-platelet interaction. Therefore, the higher unfolded VWF levels in APS could in part explain the association of APS and thrombotic complications.

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