siRNA-based therapeutic approaches for rheumatic diseases

被引:40
|
作者
Apparailly, Florence [1 ]
Jorgensen, Christian [1 ]
机构
[1] Univ Hosp Montpellier, INSERM, U844, F-34295 Montpellier, France
关键词
SMALL INTERFERING RNA; COLLAGEN-INDUCED ARTHRITIS; IN-VIVO DELIVERY; MURINE ARTHRITIS; DENDRITIC CELLS; DRUG-DELIVERY; GENE; OSTEOARTHRITIS; CHONDROCYTES; OSTEOPONTIN;
D O I
10.1038/nrrheum.2012.176
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
RNA interference (RNAi) is one of the most exciting and important discoveries of the past few decades. Small interfering RNAs (siRNAs) can silence gene activity and be used to interfere with pathophysiological processes. Substantial research has focused on introducing 'drug-like' properties-stability, selectivity and potency-to RNAi molecules, and clinical trials have been initiated. Despite initial success, the current challenge that remains is to develop optimized vehicles that avoid off-target effects whilst efficiently delivering the therapeutic siRNA to specific cell types. As for many other diseases, siRNA-based therapy is emerging as a promising approach for the treatment of rheumatic disorders. Although the pathogenesis of rheumatic diseases is complex, identification of candidate genes able to influence either inflammation or structural damage has been successful. Here, we will discuss advances in the field and potential applications of siRNA therapeutics in clinical trials for rheumatic conditions. Apparailly, F. & Jorgensen, C. Nat. Rev. Rheumatol. 9, 56-62 (2013); published online 23 October 2012; doi:10.1038/nrrheum.2012.176
引用
收藏
页码:56 / 62
页数:7
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