Molecular Biology and Inhibitors of Hepatitis A Virus

被引:26
作者
Debing, Yannick [1 ]
Neyts, Johan [1 ]
Thibaut, Hendrik Jan [1 ]
机构
[1] Univ Leuven, Rega Inst Med Res, Leuven, Belgium
关键词
hepatitis A virus; virus replication; immune evasion; atopy; antiviral drugs; INTRACELLULAR MEMBRANE REARRANGEMENTS; CYSTEINE PROTEINASE-INHIBITORS; SITE-MEDIATED TRANSLATION; SMALL INTERFERING RNAS; 5 NONTRANSLATED REGION; MONKEY KIDNEY-CELLS; HAV 3C PROTEINASE; ENTRY SITE; IN-VITRO; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE;
D O I
10.1002/med.21292
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Hepatitis A virus (HAV) is a faeco-orally transmitted picornavirus and is one of the main causes of acute hepatitis worldwide. An overview of the molecular biology of HAV is presented with an emphasis on recent findings. Immune evasion strategies and a possible correlation between HAV and atopy are discussed as well. Despite the availability of efficient vaccines, antiviral drugs targeting HAV are required to treat severe cases of fulminant hepatitis, contain outbreaks, and halt the potential spread of vaccine-escape variants. Additionally, such drugs could be used to shorten the period of illness and decrease associated economical costs. Several known inhibitors ofHAVwith various mechanisms of action will be discussed. Since none of these molecules is readily useable in the clinic and since the availability of an anti-HAV drug would be of clinical importance, increased efforts should be targeted toward discovery and development of such antivirals. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:895 / 917
页数:23
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