期刊论文详细信息
Arthritis Research & Therapy
TLR2 modulates inflammation in zymosan-induced arthritis in mice
Alexander So1  Nathalie Busso1  Veronique Chobaz-Péclat1  David Tarussio1  Matthias E Frasnelli1 
[1]Laboratoire de Rhumatologie, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland
关键词: Toll-like receptor;    monocytes/macrophages;    immune system;    chronic inflammation;   
Others  :  1101099
DOI  :  10.1186/ar1494
 received in 2004-10-15, accepted in 2004-12-10,  发布年份 2005
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【 摘 要 】

The interplay between the innate and acquired immune systems in chronic inflammation is not well documented. We have investigated the mechanisms of inflammation in murine zymosan-induced arthritis (ZIA) in the light of recent data on the roles of Toll-like receptor 2 (TLR2) and Dectin-1 in the activation of monocyte/macrophages by zymosan. The severity of inflammation, joint histology, lymphocyte proliferation and antibody production in response to zymosan were analyzed in mice deficient in TLR2 and complement C3, and the effects of Dectin-1 inhibition by laminarin were studied. In comparison with wild-type animals, TLR2-deficient mice showed a significant decrease in the early (day 1) and late phases (day 24) of joint inflammation. C3-deficient mice showed no differences in technetium uptake or histological scoring. TLR2-deficient mice also showed a significant decrease in lymph node cell proliferation in response to zymosan and a lower IgG antibody response to zymosan at day 25 in comparison with wild-type controls, indicating that TLR2 signalling has a role in the development of acquired immune responses to zymosan. Although laminarin, a soluble β-glucan, was able to significantly inhibit zymosan uptake by macrophages in vitro, it had no effect on ZIA in vivo. These results show that ZIA is more prolonged than was originally described and involves both the innate and acquired immune pathways. C3 does not seem to have a major role in this model of joint inflammation.

【 授权许可】

   
2005 Frasnelli et al.; licensee BioMed Central Ltd.

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