Qin Yan-li, Zhang Ji-ming, Huang Yu-xian, Mao Ri-cheng, Yin You-kuan, Zhang Wan-qin, Zhang Qing-bo, Wu Xiang-hui, Weng Xin-hua
Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai 200040, China.
Zhonghua Gan Zang Bing Za Zhi. 2007 Jan;15(1):4-7.
To study the resistant rate of hepatitis B virus (HBV) to ADV and the dynamic evolution of HBV in lamivudine (Lam)-resistant chronic hepatitis B (CHB) patients.
Twenty-three Lam-resistant CHB patients were assigned to a 10mg/d ADV monotherapy for 68-116 weeks. The baseline and different time point blood samples after ADV monotherapy were analyzed for ADV-resistant mutations using direct sequencing of PCR products; the evolution of HBV mutations was examined by clonal analysis of serial samples from one patient infected with ADV-associated resistant HBV strains.
The cumulative incidence of genotypic ADV resistance at weeks 48 and 96 was 4.3% and 10.5% respectively respectively. The evolution analysis of HBV mutant strains in an ADV-resistant CHB patient showed that the proportion of YMDD mutants gradually decreased with rtA181S mutants increasing over time after ADV monotherapy, and that rtA181S+N236T mutants became the predominant strains during prolonged ADV monotherapy. The addition of Lam to the ongoing ADV treatment had poorer antiviral response in the patient with rtA181S or rtA181S+N236T mutant infection; one clone with multi-drug resistant mutations was selected during Lam and ADV combination therapy.
Increased risk of adefovir resistance and selection of multi-drug resistant mutations are associated with long-term ADV monotherapy in patients with Lam-resistant chronic hepatitis B.
研究乙型肝炎病毒(HBV)对阿德福韦酯(ADV)的耐药率以及拉米夫定(Lam)耐药的慢性乙型肝炎(CHB)患者体内HBV的动态演变。
23例拉米夫定耐药的CHB患者接受10mg/d阿德福韦酯单药治疗68 - 116周。采用PCR产物直接测序法分析阿德福韦酯单药治疗后基线及不同时间点血样中的阿德福韦酯耐药突变;通过对1例感染阿德福韦酯相关耐药HBV毒株患者的系列样本进行克隆分析,研究HBV突变的演变情况。
48周和96周时基因型阿德福韦酯耐药的累积发生率分别为4.3%和10.5%。对1例阿德福韦酯耐药的CHB患者HBV突变株的演变分析显示,阿德福韦酯单药治疗后,随着rtA181S突变株比例随时间增加,YMDD突变株比例逐渐下降,且在长期阿德福韦酯单药治疗期间rtA181S + N236T突变株成为优势毒株。在正在接受阿德福韦酯治疗的患者中加用拉米夫定,对于感染rtA181S或rtA181S + N236T突变株的患者抗病毒反应较差;在拉米夫定与阿德福韦酯联合治疗期间选择出1个具有多药耐药突变的克隆。
阿德福韦酯耐药风险增加及多药耐药突变的选择与拉米夫定耐药的慢性乙型肝炎患者长期阿德福韦酯单药治疗有关。