Expression of the inflammatory chemokines CCL5, CCL3 and CXCL10 in juvenile idiopathic arthritis, and demonstration of CCL5 production by an atypical subset of CD8+ T cells.docVIP
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ExpressionoftheinflammatorychemokinesCCL5,CCL3andCXCL10injuvenileidiopathicarthritis,anddemonstrationofCCL5productionbyanatypicalsubsetofCD8Tcells
Available online /content/8/2/R50
Research article
Open Access
Vol 8 No 2
Expression of the inflammatory chemokines CCL5, CCL3 and
CXCL10 in juvenile idiopathic arthritis, and demonstration of CCL5
production by an atypical subset of CD8+ T cells
Daniel S Pharoah1, Hemlata Varsani1, Richard W Tatham1, Katy R Newton1, Wilco de Jager2,
Berent J Prakken2, Nigel Klein3 and Lucy R Wedderburn1
1Rheumatology Unit, Institute of Child Health, UCL, London, UK
2Department of Paediatric Immunology, Wilhelmina Childrens Hospital, University Medical Centre, Utrecht
3Microbiology/Infectious Disease Unit, Institute of Child Health, UCL, London, UK
Corresponding author: Lucy R Wedderburn, l.wedderburn@ich.ucl.ac.uk
Received: 4 Oct 2005 Revisions requested: 26 Oct 2005 Revisions received: 16 Jan 2006 Accepted: 6 Feb 2006 Published: 28 Feb 2006
Arthritis Research Therapy 2006, 8:R50 (doi:10.1186/ar1913)
This article is online at: /content/8/2/R50
? 2006 Pharoah et al.; licensee BioMed Central Ltd.
This is an open access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
This study focuses upon three chemokines, namely CCL5,
CXCL10 and CCL3, which are potential novel therapeutic
targets in arthritis. The aim of the study was to analyse the
expression and production of these three chemokines within the
joints of children with juvenile idiopathic arthritis (JIA) of the
oligoarticular and polyarticular subtypes. All three of these
chemokines are highly expressed at the level of mRNA, with the
most significant increase in mRNA levels being demonstrated
for CCL5 when compared with matched peripheral blood
samples and controls. We show that high levels of all three
chemokines are present in synovial fluid of children with JIA. We
investigate the
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