JCR Japan College of Rheumatology-
有限責任中間法人 日本リウマチ学会
  会員専用ページ

トップページ
学会案内
沿革
定款
役員・委員会
名誉会員・評議員
学術集会
総会学術集会
歴代総会・学術集会
支部・学術集会
学会教育研修会
国際関連学会
認定制度
リウマチ専門医
リウマチ指導医
教育施設
学会出版物
学会誌MR
NLリウマチ
リウマチ学用語集
会員手続き
本サイトについて
よくある質問
関連リンク集
サイトマップ
プライバシー

MODERN RHEUMATOLOGY Vol.12 No.2

>MR12-2

Chemokines and chemokine receptors in the pathogenesis of systemic sclerosis
O. Distler1, J. Distler1, O. Kowal-Bielecka , R. E. Gay1, U. Muller-Ladner3, S. Gay1
(1)WHO Collaborating Center for Molecular Biology and Novel Therapeutic Strategies for Rheumatic Diseases, University Hospital Zurich, CH-8091 Zurich, Switzerland
(2)Department of Rheumatology and Internal Medicine, Medical Academy of Bia^ystok, Bia^ystok, Poland
(3)Department of Internal Medicine I, University of Regensburg, Regensburg, Germany
 
Full Text
  > Click Here (member's only)
 
Abstract
Abstract Activation of the immune system and increased synthesis of extracellular matrix proteins by fibroblasts are hallmarks in the pathogenesis of systemic sclerosis (SSc). The mechanisms that initiate the accumulation of inflammatory cells are still unknown. Chemokines are a family of small molecules that are divided into subfamilies according to the position of NH2-terminal cysteine motif. A new nomenclature for chemokines recently has been introduced in an attempt to overcome the confusion resulting from a number of different names for the same chemokines. Recent data indicate that chemokines, and in particular MCP-1 (CCL2), might be involved in the pathogenesis of SSc at different levels. MCP-1 is highly upregulated in skin specimens from SSc patients compared with those from healthy controls. Dermal fibroblasts release MCP-1, which is able to induce and perpetuate the migration of inflammatory cells into the skin. Interestingly, data from animal models, as well as from in vitro studies, indicate that MCP-1 might also be involved in the increased synthesis of extracellular matrix proteins, by either direct or indirect mechanisms. In conclusion, chemokines represent interesting candidates for target-directed therapies for SSc. This concept has to be confirmed by further studies using animal models for SSc and other fibrotic diseases.
 
Key words
Key words Chemokine receptors ・ Chemokines ・ Monocyte chemoattractant protein-1 (MCP-1) ・ Systemic sclerosis (SSc)
 
一覧に戻る

Copyright Japan College of Rheumatology All rights reserved.