医学
类风湿性关节炎
离体
体内
关节炎
炎症
药理学
炎性关节炎
受体
免疫学
脂多糖
腺苷
内科学
生物
生物技术
作者
Iain B. McInnes,Simon Cruwys,Keith Bowers,Martin Braddock
出处
期刊:PubMed
日期:2014-10-08
卷期号:32 (6): 878-82
被引量:51
摘要
This paper aims to explore the functional significance of the P2X7 receptor in preclinical models of rheumatoid arthritis.Preclinical studies in vivo were performed using the rat streptococcal cell wall (SCW) arthritis model. Ex vivo cultures of lipopolysaccharide (LPS)/benzoylbenzoyl adenosine triphosphate (BzATP)-stimulated human monocytes were generated to test the activities of a novel, highly specific inhibitor of human P2X7, AZD9056, on interleukin (IL)-1 and IL-18 release.P2X7 receptor expression was detected in inflamed synovial tissue after onset of SCW-induced arthritis in rats. Inhibition of P2X7 therein led to reduced articular inflammation and erosive progression. No effect was noted on acute-phase responses. Ex vivo, AZD9056 inhibited IL-1 and IL-18 release to BzATP in LPS-primed human monocytes.P2X7 receptor inhibition could represent a novel approach to the treatment of inflammatory arthritis. However, confirmatory clinical studies are warranted to further explore this possibility.
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