Zhang Fangjie, Luo Wei, Li Yusheng, Gao Shuguang, Lei Guanghua
Department of Orthopaedics, Xiangya Hospital, Central South University, No. 87 Xiangya Road, Changsha, 410008, Hunan, China.
Rheumatol Int. 2015 Apr;35(4):589-95. doi: 10.1007/s00296-014-3122-z. Epub 2014 Aug 28.
Rheumatoid arthritis (RA) is a chronic inflammatory disease characterized by joint swelling, joint tenderness, and destruction of synovial joints, leading to severe disability and premature mortality. RA is a multifactorial disease with genetic, environmental, and stochastic components related to its susceptibility. It has been demonstrated that the expression of osteopontin (OPN) is upregulated in the RA patients. Numerous studies have indicated that the full-length OPN or even OPN fragments, such as thrombin-cleaved OPN and its receptors, play the key roles in RA pathogenesis. Therapeutic application of siRNA to target OPN or neutralizing antibodies related to OPN epitopes in RA animal models are in progress, and some results are encouraging. However, there is a long way to go along with the clinical trials. This review focuses on the recent development in research associated with the OPN role in the pathogenesis of RA and provides insights concerning the OPN targeting as therapeutic approaches for patients with RA.
类风湿关节炎(RA)是一种慢性炎症性疾病,其特征为关节肿胀、压痛以及滑膜关节破坏,可导致严重残疾和过早死亡。RA是一种多因素疾病,其易感性与遗传、环境和随机因素有关。已有研究表明,骨桥蛋白(OPN)在RA患者中的表达上调。大量研究表明,全长OPN甚至OPN片段,如凝血酶切割的OPN及其受体,在RA发病机制中起关键作用。在RA动物模型中,针对OPN的siRNA治疗应用或与OPN表位相关的中和抗体正在进行中,一些结果令人鼓舞。然而,距离临床试验还有很长的路要走。本综述重点关注OPN在RA发病机制中的作用的最新研究进展,并提供有关将OPN作为RA患者治疗方法的见解。