Department of Rheumatology, Cardiff University, Heath Park, Cardiff CF144XN, UK.
Curr Drug Targets. 2010 May;11(5):576-85. doi: 10.2174/138945010791011965.
The great success of targeted biologic therapy against rheumatoid arthritis (RA) in recent years has meant that much research has been devoted to investigating the pathophysiology of osteoarthritis (OA) in the hope of defining novel therapeutic targets. In contrast to RA, with its pannus and erosions, OA has long been thought of as a degenerative disease of cartilage, with secondary bony damage and osteophytes. But in recent years, the importance of the synovium, and in particular the synovial macrophages, in OA, has been highlighted in both in vitro and in vivo studies. This review will discuss the potential of synovial macrophages and their mediators, in particular the proinflammatory cytokines tumour necrosis factor alpha and interleukin-1, as potential therapeutic targets in OA.
近年来,针对类风湿关节炎(RA)的靶向生物治疗取得了巨大成功,这意味着大量研究致力于探讨骨关节炎(OA)的病理生理学,以期确定新的治疗靶点。与具有滑膜增生和侵蚀的 RA 不同,OA 长期以来一直被认为是软骨的退行性疾病,伴有继发性骨损伤和骨赘。但近年来,滑膜尤其是滑膜巨噬细胞在 OA 中的作用在体外和体内研究中都得到了强调。这篇综述将讨论滑膜巨噬细胞及其介质(特别是促炎细胞因子肿瘤坏死因子-α和白细胞介素-1)作为 OA 潜在治疗靶点的可能性。