Targets of emerging therapies for viral hepatitis B and C

被引:4
|
作者
Yerly, Daniel
Di Giammarino, Loriana
Bihl, Florian
Cerny, Andreas [1 ]
机构
[1] Univ Bern, Clin Rheumatol & Clin Immunol Allergol, CH-3010 Bern, Switzerland
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Gastrointestinal Unit, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Partners AIDS Res Ctr, Boston, MA 02114 USA
[5] Osped Reg Lugano, Dept Med, CH-6903 Lugano, Switzerland
关键词
gene therapy; hepatitis B virus; hepatitis C virus; immune therapy; nucleoside analogue; nucleotide analogue; polymerase inhibitor; protease inhibitor; therapeutic vaccine;
D O I
10.1517/14728222.10.6.833
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Viral hepatitis B and C, structurally two completely different viruses, commonly infect human hepatocytes and cause similar clinical manifestations. Since their discovery, IFN has been a pillar in the treatment. However, because of the different natures of the viruses, therapeutic approaches diverge and new treatment targets are tailored specifically for each virus. Herein, the authors analyse therapeutic approaches for hepatitis B virus (HBV) and hepatitis C virus (HCV) and focus on emerging concepts that are under clinical evaluation. In particular, promising viral inhibitors for HBV and HCV are reviewed and the current status of research for gene therapy for HCV is described. Immune therapy is a fast-moving field with fascinating results which include therapeutic vaccines and toll-like receptor agonists that could improve tomorrow's treatment approaches.
引用
收藏
页码:833 / 850
页数:18
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