共 78 条
Strategies to develop antivirals against enterovirus 71
被引:51
作者:

Kuo, Rei-Lin
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机构:
Chang Gung Univ, Res Ctr Emerging Viral Infect, Tao Yuan, Taiwan
Chang Gung Univ, Coll Med, Dept Med Biotechnol & Lab Sci, Tao Yuan, Taiwan Chang Gung Univ, Res Ctr Emerging Viral Infect, Tao Yuan, Taiwan

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机构:
机构:
[1] Chang Gung Univ, Res Ctr Emerging Viral Infect, Tao Yuan, Taiwan
[2] Chang Gung Univ, Coll Med, Dept Med Biotechnol & Lab Sci, Tao Yuan, Taiwan
[3] Natl Hlth Res Inst, Inst Biotechnol & Pharmaceut Res, Miaoli, Taiwan
来源:
关键词:
CENTRAL-NERVOUS-SYSTEM;
RHINOVIRUS 3C PROTEASE;
MOUTH-DISEASE;
AURINTRICARBOXYLIC ACID;
RNA INTERFERENCE;
VP1;
PROTEIN;
IN-VITRO;
SELECTIVE-INHIBITION;
CYNOMOLGUS MONKEYS;
CLINICAL-FEATURES;
D O I:
10.1186/1743-422X-10-28
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Enterovirus 71 (EV71) is an important human pathogen which may cause severe neurological complications and death in children. The virus caused several outbreaks in the Asia-Pacific region during the past two decades and has been considered a significant public health problem in the post-poliovirus eradication era. Unlike poliovirus, there is no effective vaccine or approved antivirals against EV71. To explore anti-EV71 agents therefore is of vital importance. Several strategies have been employed to develop antivirals based on the molecular characteristics of the virus. Among these, some small molecules that were developed against human rhinoviruses and poliovirus are under evaluation. In this review, we discuss the recent development of such small molecules against EV71, known drug resistance and possible solutions to it, and animal models for evaluating the efficacy of these antivirals. Although further investigation is required for clinical applications of the existing candidates, the molecular mechanisms revealed for the inhibition of EV71 replication can be used for designing new molecules against this virus in the future.
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