Thromb Haemost 2013; 109(01): 72-78
DOI: 10.1160/TH12-05-0346
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Endothelial microparticle release is stimulated in vitro by purified IgG from patients with the antiphospholipid syndrome

Charis Pericleous
1   Centre for Rheumatology, Division of Medicine University College London, Rayne Institute, London, UK
,
Lindsey A. Clarke
2   Institute of Child Health University College London, London, UK
,
Paul A. Brogan
2   Institute of Child Health University College London, London, UK
,
David S. Latchman
1   Centre for Rheumatology, Division of Medicine University College London, Rayne Institute, London, UK
,
David A. Isenberg
1   Centre for Rheumatology, Division of Medicine University College London, Rayne Institute, London, UK
,
Yiannis Ioannou
1   Centre for Rheumatology, Division of Medicine University College London, Rayne Institute, London, UK
,
Ian P. Giles
1   Centre for Rheumatology, Division of Medicine University College London, Rayne Institute, London, UK
,
Anisur Rahman
1   Centre for Rheumatology, Division of Medicine University College London, Rayne Institute, London, UK
› Author Affiliations
Financial support: C.P and L.C were funded by the Nuffield Foundation (Oliver Bird Rheumatism Programme). C.P and Y.I were funded by Arthritis Research UK (Programme Grant 19423 and Clinician Scientist Fellowship 43300). I.G acknowledges support from the Rosetrees Trust.
Further Information

Publication History

Received: 24 May 2012

Accepted after major revision: 09 October 2012

Publication Date:
27 November 2017 (online)

Summary

IgG antiphospholipid antibodies (aPL) exert direct effects on various cell types, contributing to the pathogenesis of thrombosis and pregnancy morbidity in patients with the antiphospholipid syndrome (APS). Some IgG samples from these patients activate endothelial cells (EC) in vitro as judged by surface expression of adhesion molecules such as E-selectin, which can promote thrombosis. Endothelial micro-particles (EMP), which themselves are potentially prothrombotic, are released by activated EC. Though elevated circulating EMP levels have been reported in patients with APS, it is not known whether these EMP are released due to a direct effect of aPL on the cells. We tested the effect of purified polyclonal IgG from patients with APS (APS-IgG) and healthy controls (HC-IgG) upon cultured human umbilical vein EC (HUVEC). HUVEC exposed to APS-IgG produced significantly more EMP than those exposed to HC-IgG (p=0.0036) and a greater proportion of these EMP carried surface E-selectin (6.2% ± 4.0 for APS-IgG vs. 3.4% ± 2.0 for HC IgG, p=0.0172). This study therefore demonstrates that purified polyclonal APS-IgG can drive EMP release. We propose that EMP generation may be a useful measure of aPL-mediated pathogenic effects upon EC.

 
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