Peripheral blood but not synovial fluid natural killer T cells are biased towards a Th1-like phenotype in rheumatoid arthritis 英文参考文献.docVIP
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Peripheral blood but not synovial fluid natural killer T cells are biased towards a Th1-like phenotype in rheumatoid arthritis 英文参考文献
Available online /content/7/3/R493
Research article
Open Access
Vol 7 No 3
Peripheral blood but not synovial fluid natural killer T cells are
biased towards a Th1-like phenotype in rheumatoid arthritis
Loes Linsen, Marielle Thewissen, Kurt Baeten, Veerle Somers, Piet Geusens, Jef Raus and
Piet Stinissen
Biomedisch Onderzoeksinstituut, Limburgs Universitair Centrum and School of Life Sciences, Transnationale Universiteit Limburg, Universitaire
Campus, Diepenbeek, Belgium
Corresponding author: Piet Stinissen, piet.stinissen@luc.ac.be
Received: 13 Oct 2004 Revisions requested: 17 Nov 2004 Revisions received: 14 Jan 2005 Accepted: 19 Jan 2005 Published: 18 Feb 2005
Arthritis Research Therapy 2005, 7:R493-R502 (DOI 10.1186/ar1695)
This article is online at: /content/7/3/R493
? 2005 Linsen 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
Natural killer T (NKT) cells have been implicated in the regulatory
immune mechanisms that control autoimmunity. However, their
precise role in the pathogenesis of rheumatoid arthritis (RA)
nonresponders
expanded
upon
stimulation
with
α-
galactosylceramide. Analysis of the cytokine profile of CD4+ and
CD4- PBMC derived NKT cell lines from RA patients revealed a
remains
unclear.
The
frequency,
cytokine
profile
and
significantly reduced number of IL-4 producing cells. In contrast,
synovial fluid derived NKT cell lines exhibited a Th0-like
phenotype, which was comparable to that in healthy control
individuals. This suggests that synovial fluid NKT cells are
functional, even in patients with nonresponding NKT cells in
their blood. We conclude that, because the number of
Vα24+Vβ11+CD3+ NKT cells is decreased and the cytokine
profile of
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