Does RNA interference provide new hope for control of chronic hepatitis B infection?

被引:12
|
作者
Wilson, Rachel [1 ,2 ]
Purcell, Damian [3 ]
Netter, Hans J. [2 ]
Revill, Peter A. [1 ,2 ]
机构
[1] Victorian Infect Dis Reference Lab, Melbourne, Vic, Australia
[2] Monash Univ, Dept Microbiol, Clayton, Vic 3168, Australia
[3] Univ Melbourne, Dept Microbiol, Parkville, Vic 3052, Australia
关键词
RATIONAL SIRNA DESIGN; LONG-TERM SUPPRESSION; IN-VIVO DELIVERY; GENE-EXPRESSION; ADEFOVIR DIPIVOXIL; VIRUS-REPLICATION; TRANSLATIONAL REPRESSION; MICRORNA EXPRESSION; MESSENGER-RNAS; LET-7; MICRORNA;
D O I
10.3851/IMP1424
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Hepatitis B virus (HBV) infection is a global human health problem, with an estimated 350 million people having chronic hepatitis B (CHB) infection worldwide. The majority of infections acquired during adulthood are resolved without intervention; however, infections acquired at birth or during early childhood have a 90% chance of progressing to CHB, leading to a host of adverse effects on the liver, including cirrhosis and cancer. CHB is currently treated with a combination of cytolkines and/or nucleoside/nucleotide analogues; however, adverse side effects to cytokine therapy and the selection of resistance mutations to nucleoside analogues often abrogate the efficacy of treatment. The recent discovery that small interfering RNA and microRNA are active in mammalian cells suggests it might be possible to supplement existing HBV therapies with small RNA-based therapeutic(s).
引用
收藏
页码:879 / 889
页数:11
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