D-BOARD European Consortium for Biomarker Discovery, Faculty of Medicine and Health Sciences, The University of Nottingham, Nottingham, UK,
Curr Rheumatol Rep. 2013 Dec;15(12):385. doi: 10.1007/s11926-013-0385-4.
Biological therapy is a thriving area of research and development, and is well established for chronic forms of rheumatoid arthritis (RA) and ankylosing spondylitis (AS). However, there is no clinically validated biological therapy for osteoarthritis (OA). Chronic forms of OA are increasingly viewed as an inflammatory disease. OA was largely regarded as a "wear and tear disease". However, the disease is now believed to involve "low grade" inflammation and the growth of blood vessels and nerves from the subchondral bone into articular cartilage. This realization has focused research effort on the development and evaluation of biological therapy that targets proinflammatory mediators, angiogenic factors and cytokines in articular cartilage, subchondral bone and synovium in chronic forms of OA. This review article provides an overview of emerging biological therapy for OA, and discusses recent molecular targets implicated in angiogenesis and neurogenesis and progress with antibody-based therapy, calcitonin, and kartogenin, the small molecule stimulator of chondrogenesis.
生物治疗是一个蓬勃发展的研究和开发领域,在治疗慢性类风湿关节炎(RA)和强直性脊柱炎(AS)方面已经得到了很好的确立。然而,目前还没有经过临床验证的治疗骨关节炎(OA)的生物疗法。慢性 OA 现在越来越被认为是一种炎症性疾病。OA 过去主要被认为是一种“磨损性疾病”。然而,现在人们认为这种疾病涉及“低度”炎症以及来自软骨下骨的血管和神经向关节软骨生长。这种认识促使人们致力于开发和评估针对慢性 OA 中关节软骨、软骨下骨和滑膜中促炎介质、血管生成因子和细胞因子的生物治疗。本文综述了 OA 的新兴生物治疗方法,并讨论了最近与血管生成和神经生成相关的分子靶点以及抗体治疗、降钙素和软骨形成的小分子刺激剂 kartogenin 的进展。