Potential contribution of IL-17-Producing Th1 cells to defective repair activity in joint inflammation:: Partial correction with Th2-promoting conditions

被引:21
作者
Chabaud, M
Aarvak, T
Garnero, P
Natvig, JB
Miossec, P [1 ]
机构
[1] Hop Edouard Herriot, Dept Immunol, Clin Immunol Unit, F-69437 Lyon 03, France
[2] Hop Edouard Herriot, Dept Rheumatol, F-69437 Lyon, France
[3] Hop Edouard Herriot, INSERM, U403, F-69437 Lyon 03, France
[4] Univ Oslo, Natl Hosp, Inst Immunol & Rheumatol, Oslo, Norway
关键词
cytokines; cell-to-cell interactions; Th-1; Th-2; rheumatoid arthritis;
D O I
10.1006/cyto.2000.0811
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
To assess the contribution of cell interactions to the production of cytokines and type I collagen, fixed synovium T cell clones were cocultured on synoviocytes and levels of IL-6, LIF and PICP, a marker of type I collagen synthesis measured. Levels of IL-6 and LIF were higher with Th-1 than with Th-0 and Th-2 clones. Levels of PICP were decreased with Th-1 clones and increased with Th-2 clones. IL-17-producing T cells, all Th-1, were among the highest inducers of cytokine and inhibitors of collagen synthesis. Preincubation of clones in Th-2 conditions (IL-12 plus anti-IL-4) increased IL-6 production, whereas Th-2 conditions (IL-4 plus anti-IL-12) strongly inhibited IL-6 production and restored repair activity. As rheumatoid synovium is infiltrated by Th-1 cells, local cell interactions result in a pro-inflammatory pattern with defective repair, which can be reversed at least in part, by a Th-2 pattern. (C) 2001 Academic Press.
引用
收藏
页码:113 / 118
页数:6
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