Emerging anti-osteoclast therapy for rheumatoid arthritis

被引:27
作者
Tanaka, Sakae [1 ]
机构
[1] Univ Tokyo, Fac Med, Dept Orthoped Surg, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1130033, Japan
基金
日本学术振兴会;
关键词
Osteoclast; RANKL; Rheumatoid arthritis; MODIFYING ANTIRHEUMATIC DRUGS; DIFFERENTIATION FACTOR; JAPANESE PATIENTS; BONE-RESORPTION; POSTMENOPAUSAL WOMEN; JOINT DESTRUCTION; STRUCTURAL DAMAGE; FRACTURE RISK; DOUBLE-BLIND; T-CELLS;
D O I
10.1016/j.jos.2018.06.001
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Rheumatoid arthritis (RA) is an autoimmune inflammatory disorder characterized by progressive destruction of affected synovial joints. Recently, it was demonstrated that osteoclasts play critical roles in bone destruction in RA. Receptor activator of NF-kappa B ligand (RANKL), which belongs to the tumor necrosis factor superfamily, is indispensable for osteoclast differentiation and bone destruction in RA. Denosumab, a monoclonal antibody against human RANKL, not only increased bone mineral density, but also efficiently suppressed the progression of bone erosion in RA patients in a randomized controlled study. However, denosumab did not reduce the cartilage destruction or disease activity in RA, and further investigation is required to establish the appropriate positioning of denosumab in the treatment strategy of RA. (C) 2018 The Japanese Orthopaedic Association. Published by Elsevier B.V.
引用
收藏
页码:717 / 721
页数:5
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