Rheumatology Advance Access originally published online on July 20, 2009
Rheumatology 2009 48(10):1183-1184; doi:10.1093/rheumatology/kep216
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
© The Author 2009. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
Editorial |
Circulating endothelial progenitor cells in ANCA-associated vasculitis: the light at the end of the tunnel?
1Hospital Regional Publico Araguaia/IDESMA and University of São Paulo, São Paulo, Brazil
Correspondence to: Alfredo N. C. Santana, Rua Maraba 21, CEP 68550-490, Redencao, PA, Brazil. E-mail: alfredonicodemos@hotmail.com
| The first 10% of the full text of this article appears below. |
The main clinical features of ANCA-associated vasculitis (AAV) are inflammation and necrosis of small vessels, thrombus formation and endothelial injury [1–3]. In this issue of Rheumatology, Závada et al. [4] conclude that low numbers of circulating endothelial progenitor cells (EPCs) are associated with increased propensity for early relapse of AAV.
The therapeutic potential of EPCs in AAV may exist in the form of four different scenarios. First, although disease remission is achieved by most patients, morbidity (pulmonary fibrosis,