Platelet- and endothelial-derived microparticles in the context of different antiphospholipid antibody profiles

Author:

Cheng Chunyan1,Bison Elisa1,Pontara Elena1,Cattini Maria Grazia1,Tonello Marta2,Denas Gentian1,Pengo Vittorio13ORCID

Affiliation:

1. Thrombosis Research Laboratory, Department of Cardio-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, Italy

2. Department of Medicine, Rheumatology Section, University of Padua, Padova, Italy

3. Arianna Foundation on Anticoagulation, Bologna, Italy

Abstract

Objectives Studies on microparticles (MPs) in patients with antiphospholipid antibodies (aPL) are sparse and inconclusive. The relation between MPs and different aPL antibody profiles has never been tested. We evaluated the presence of platelet and endothelial microparticles in patients positive for IgG anti-β2-glycoprotein I (aβ2GPI) antibodies according to triple, double and single positive aPL profiles. Methods Megamix (Biocytex) was used to set up the MPs gating according to the datasheet. Markers of Platelet Microparticles (PMPs) were CD41a-PE and annexin-V-FITC that was used to determine phosphatidylserine (PS) exposure. CD144-FITC was used as a marker of Endothelial Microparticles (EMPs). Results The number of total MPs and EMPs was significantly higher in triple positive groups with respect to single positive group and showed a significant correlation with IgG aβ2GPI titers. The number PMPs was the lowest in triple positive group and inversely correlated with IgG aβ2GPI titers. Conclusions Elevated levels of total MPs and EMPs suggest a state of vascular activation in IgG aβ2GPI positive individuals according to the number of positive tests. PMPs may be fast cleared from circulation in high risk triple positive patients.

Publisher

SAGE Publications

Subject

Rheumatology

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