Division of Rheumatology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Ther Adv Musculoskelet Dis. 2012 Oct;4(5):369-77. doi: 10.1177/1759720X12447705.
The inflammatory myopathies are a heterogeneous group of disorders characterized by muscle weakness and inflammation. Although no standard therapeutic guidelines exist, traditional treatment has included corticosteroids and a variety of second-line immunosuppressants. As treatment of refractory disease has been difficult, newer agents and approaches have been used with varying response. The advent of standardized treatment response criteria by the International Myositis Assessment and Clinical Studies (IMACS) group has helped investigators to evaluate and compare clinical trial outcomes in a more rigorous fashion. The use of intravenous immunoglobulin (IVIG), rituximab, biologic agents including tumor necrosis factor (TNF) inhibitors, stem-cell transplantation, gene therapy, and vascular occlusion resistance training are reviewed here. As our understanding of disease pathogenesis at the immunologic, genetic, and molecular level expands, the discovery of novel therapeutic targets hold promise for the successful treatment of these conditions.
炎性肌病是一组以肌肉无力和炎症为特征的异质性疾病。虽然没有标准的治疗指南,但传统的治疗方法包括皮质类固醇和各种二线免疫抑制剂。由于难治性疾病的治疗一直很困难,因此已经使用了各种新型药物和方法,但反应各不相同。国际肌炎评估和临床研究 (IMACS) 小组制定的标准化治疗反应标准的出现,帮助研究人员以更严格的方式评估和比较临床试验结果。本文综述了静脉注射免疫球蛋白 (IVIG)、利妥昔单抗、生物制剂(包括肿瘤坏死因子 (TNF) 抑制剂)、干细胞移植、基因治疗和血管闭塞阻力训练的应用。随着我们在免疫、遗传和分子水平上对疾病发病机制的理解的扩展,发现新的治疗靶点有望成功治疗这些疾病。