Enhanced late-outgrowth circulating endothelial progenitor cell levels in rheumatoid arthritis and correlation with disease activity.docVIP
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Enhanced late-outgrowth circulating endothelial progenitor cell levels in rheumatoid arthritis and correlation with disease activity
Jodon de Villeroché et al. Arthritis Research Therapy 2010, 12:R27
/content/12/1/R27
RESEARCH ARTICLE
Open Access
Enhanced late-outgrowth circulating endothelial Research article
progenitor cell levels in rheumatoid arthritis and
correlation with disease activity
Vanina Jodon de Villeroché1, Jérome Avouac1,2, Aurélie Ponceau1, Barbara Ruiz1, André Kahan2, Catherine Boileau1,3,
Georges Uzan4 and Yannick Allanore*1,2
Abstract
Introduction: Angiogenesis and vasculogenesis are critical in rheumatoid arthritis (RA) as they could be a key issue for
chronic synovitis. Contradictory results have been published regarding circulating endothelial progenitor cells (EPCs) in
RA. We herein investigated late outgrowth EPC sub-population using recent recommendations in patients with RA and
healthy controls.
Methods: EPCs, defined as Lin-/7AAD-/CD34+/CD133+/VEGFR-2+ cells, were quantified by flow cytometry in
peripheral blood mononuclear cells (PBMCs) from 59 RA patients (mean age: 54 ± 15 years, disease duration: 16 ± 11
years) and 36 controls (mean age: 53 ± 19 years) free of cardiovascular events and of cardiovascular risk factors.
Concomitantly, late outgrowth endothelial cell colonies derived from culture of PBMCs were analyzed by colony-
forming units (CFUs).
Results: RA patients displayed higher circulating EPC counts than controls (median 112 [27 to 588] vs. 60 [5 to 275]) per
million Lin- mononuclear cells; P = 0.0007). The number of circulating EPCs positively correlated with disease activity
reflected by DAS-28 score (r = 0.43; P = 0.0028) and lower counts were found in RA patients fulfilling remission criteria (P
= 0.0069). Furthermore, late outgrowth CFU number was increased in RA patients compared to controls. In RA, there
was no association between the number of EPCs and serum markers of inflammation or endothelial injury or synovitis.
Conclusions: Our data, based on a well characterized definition of late outgrowth EPCs, demonstrate enhanced le
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