Naturally occurring hepatitis C virus protease inhibitors resistance-associated mutations among chronic hepatitis C genotype 1b patients with or without HIV co-infection

被引:6
作者
Cao, Ying [1 ]
Zhang, Yu [1 ]
Bao, Yi [3 ]
Zhang, Renwen [1 ]
Zhang, Xiaxia [1 ]
Xia, Wei [2 ]
Wu, Hao [2 ]
Xu, Xiaoyuan [1 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Hosp 1, Dept Infect Dis, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Youan Hosp, Dept Infect Dis, Beijing, Peoples R China
[3] Shiyan Taihe Hosp, Dept Neurol, Shiyan, Peoples R China
基金
中国国家自然科学基金;
关键词
hepatitis C virus; HIV/hepatitis C virus co-infection; non-structural 3 protease inhibitor; resistance mutation; TREATMENT-NAIVE PATIENTS; INTERFERON-ALPHA; 2A; ANTIVIRAL RESISTANCE; PLUS RIBAVIRIN; PHASE-3; TRIAL; DOUBLE-BLIND; INFECTION; SIMEPREVIR; THERAPY; CHINA;
D O I
10.1111/hepr.12590
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The aim of this study was to measure the frequency of natural mutations in hepatitis C virus (HCV) mono-infected and HIV/HCV co-infected protease inhibitor (PI)-naive patients. Methods: Population sequence of the non-structural (NS) 3 protease gene was evaluated in 90 HCV mono-infected and 96 HIV/HCV co-infected PI treatment-naive patients. The natural prevalence of PI resistance mutations in both groups was compared. Results: Complete HCV genotype 1b NS3 sequence information was obtained for 152 (81.72%) samples. Seven sequences (8.33%) of the 84 HCV mono-infected patients and 21 sequences (30.88%) of the 68 HIV/HCV co-infected patients showed amino acid substitutions associated with HCV PI resistance. There was a significant difference in the natural prevalence of PI resistance mutations between these two groups (P = 0.000). The mutations T54S, R117H and N174F were observed in 1.19%, 5.95% and 1.19% of HCV mono-infected patients. The mutations F43S, T54S, Q80K/R, R155K, A156G/V, D168A/E/G and V170A were found in 1.47%, 4.41%, 1.47%/1.47%, 2.94%, 23.53%/1.47%, 1.47%/1.47%/1.47% and 1.47% of HIV/HCV co-infected patients, respectively. In addition, the combination mutations in the NS3 region were detected only in HIV/HCV genotype 1b co-infected patients. Conclusion: Naturally occurring HCV PI resistance mutations existed in HCV mono-infected and HIV/HCV co-infected genotype 1b PI-naive patients. HIV co-infection was associated with a greater frequency of PI resistance mutations. The impact of HIV infection on baseline HCV PI resistance mutations and treatment outcome in chronic hepatitis C (CHC) patients should be further analyzed.
引用
收藏
页码:552 / 558
页数:7
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