New short interfering RNA-based therapies for glomerulonephritis

被引:6
|
作者
Shimizu, Hideki [1 ]
Fujita, Toshiro [1 ]
机构
[1] Univ Tokyo, Sch Med, Dept Nephrol & Endocrinol, Bunkyo Ku, Tokyo 1138655, Japan
关键词
B-VIRUS REPLICATION; POLYION COMPLEX MICELLES; INNATE IMMUNE-RESPONSE; DRUG-DELIVERY SYSTEMS; IN-VIVO; GENE DELIVERY; SIRNA DELIVERY; MODIFIED POLYETHYLENIMINES; NONHUMAN-PRIMATES; KIDNEY-DISEASE;
D O I
10.1038/nrneph.2011.61
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Current treatments for glomerulonephritis are not satisfactory, and the development of new therapies would be indispensable. Short interfering RNAs (siRNAs) are promising candidates for molecular therapy because of their strong and specific gene-silencing effects. Despite rapid progress in research into the therapeutic uses of siRNAs, however, many hurdles must be overcome before siRNA-based therapies can be brought to the clinic. Most in vivo studies of siRNA-based therapy have been limited to local administration or delivery to specific target organs, including the liver. Therapies based on siRNAs for patients with glomerulonephritis show promise, although tissue-specific protocols using siRNAs have not yet been established for this indication. This Review aims to provide an overview of the current challenges in siRNA-based therapy, primarily with respect to glomerular targeting. In addition, novel delivery approaches for glomerulus-targeted, siRNA-based therapies are described.
引用
收藏
页码:407 / 415
页数:9
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