New strategies against drug resistance to herpes simplex virus

被引:182
作者
Jiang, Yu-Chen [1 ]
Feng, Hui [2 ]
Lin, Yu-Chun [1 ]
Guo, Xiu-Rong [3 ,4 ]
机构
[1] Sichuan Univ, West China Sch Stomatol, State Key Lab Oral Dis, Chengdu 610041, Peoples R China
[2] Cent S Univ, XiangYa Stomatol Hosp, Changsha 410078, Peoples R China
[3] Ctr Nanotechnol, Munster, Germany
[4] Sichuan Univ, West China Med Sch, Inst Nanobiomed Technol & Membrane Biol, Chengdu 610041, Peoples R China
关键词
new strategies; drug resistance; herpes simplex virus; Janus-type nucleoside analogues; lethal mutagenesis; HELICASE-PRIMASE INHIBITOR; NEW-ZEALAND SPONGE; ACYCLOVIR-RESISTANT; THYMIDINE KINASE; ANTIVIRAL ACTIVITY; GENITAL HERPES; JANUS-TYPE; TRANSPLANT RECIPIENTS; LETHAL MUTAGENESIS; DNA-POLYMERASE;
D O I
10.1038/ijos.2016.3
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Herpes simplex virus (HSV), a member of the Herpesviridae family, is a significant human pathogen that results in mucocutaneous lesions in the oral cavity or genital infections. Acyclovir (ACV) and related nucleoside analogues can, successfully treat HSV infections, but the emergence of drug resistance to ACV has created a barrier for the treatment of HSV infections, especially in immunocompromised patients. There is an urgent need to explore new and effective tactics to circumvent drug resistance to HSV. This review summarises the current strategies in the development of new targets (the DNA helicase/primase (H/P) complex), new types of molecules (nature products) and new antiviral mechanisms (lethal mutagenesis of Janus-type nucleosides) to fight the drug resistance of HSV.
引用
收藏
页码:1 / 6
页数:6
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