The role of interleukin-15 in T-cell migration and activation in rheumatoid arthritis

被引:409
|
作者
McInnes, IB
AlMughales, J
Field, M
Leung, BP
Huang, FP
Dixon, R
Sturrock, RD
Wilkinson, PC
Liew, FY
机构
[1] UNIV GLASGOW,DEPT IMMUNOL,GLASGOW G11 6NT,LANARK,SCOTLAND
[2] UNIV GLASGOW,DEPT MED,CTR RHEUMAT DIS,GLASGOW G11 6NT,LANARK,SCOTLAND
[3] LITTLEMORE HOSP,YAMANOUCHI RES INST,OXFORD OX4 4XN,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1038/nm0296-175
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin 15 (IL-15) is a novel cytokine with interleukin-2-like activity. It is also a potent T-lymphocyte chemoattractant. Rheumatoid arthritis (RA) is a chronic inflammatory disease characterized by the presence of activated T lymphocytes, macrophages and synoviocytes in the synovial membrane. The mechanisms of T-cell activation in RA are currently unclear. We report the presence of high concentrations of IL-15 in rheumatoid arthritis (RA) synovial fluid and have demonstrated its expression in the synovial membrane lining layer by immunohistochemistry. RA synovial fluids were found to contain chemotactic activity, which was attributable in part to the presence of IL-15. Moreover, in a murine model, injection of recombinant IL-15 was found to induce a local tissue inflammatory infiltrate consisting predominantly of T lymphocytes. Synovial fluid T lymphocytes proliferate in response to IL-15, demonstrating that continued responsiveness to IL-15 is a feature of T cells after entry into the synovial compartment, These data suggest that IL-15 can recruit and activate T lymphocytes into the synovial membrane, thereby contributing to RA pathogenesis.
引用
收藏
页码:175 / 182
页数:8
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