Complexity and diversity of hepatitis B virus quasispecies: Correlation with long-term entecavir antiviral efficacy

被引:20
作者
Tong, Jin [1 ]
Li, Qing-Ling [2 ]
Huang, Ai-Long [3 ]
Guo, Jin-Jun [1 ]
机构
[1] Chongqing Med Univ, Dept Gastroenterol & Hepatol, Affiliated Hosp 2, Chongqing 400010, Peoples R China
[2] Chongqing Med Univ, Inst Life Sci, Chongqing, Peoples R China
[3] Chongqing Med Univ, Key Lab Mol Biol Infect Dis, Minist Educ, Chongqing 400016, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatitis B virus; Entecavir; Genetic heterogeneity; Evolution; IMMUNE-RESPONSES; DRUG-RESISTANCE; INFECTION; DISEASE;
D O I
10.1016/j.antiviral.2013.06.020
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
This study was undertaken to determine the complexity and diversity of hepatitis B virus (HBV) quasispecies during long-term antiviral therapy and examine their impacts on therapeutic outcome. Six chronic hepatitis B patients receiving entecavir monotherapy (0.5 mg/day) for 3 years were enrolled. The reverse transcriptase region of the HBV polymerase gene was sequenced and HBV quasispecies complexity and diversity were calculated. Sustained virological response (SVR) was defined as serum HBV DNA <57 IU/ml from 48 weeks after treatment to the end of follow up. Four patients achieved a SVR and the other two had a virological breakthrough at week 24. Despite comparable baseline levels, the complexity and diversity of HBV quasispecies were significantly (p < 0.05) reduced in sustained responders versus the patients with a virological breakthrough 48 weeks after treatment. Thus, reduction in HBV quasispecies complexity and diversity may predict an SVR to long-term entecavir monotherapy. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:312 / 317
页数:6
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