HCV phylogenetic signature and prevalence of pretreatment NS5A and NS5B NI-Resistance associated substitutions in HCV-Infected patients in Mainland China

被引:19
作者
Wei, Lai [1 ]
Omata, Masao [2 ]
Lim, Young-Suk [3 ]
Xie, Qing [4 ]
Hou, Jin Lin [5 ]
Jia, Jidong [6 ]
Hedskog, Charlotte [7 ]
Martin, Ross [7 ]
Doehle, Brian [7 ]
Yang, Jenny [7 ]
De-Oertel, Shampa [7 ]
Massetto, Benedetta [7 ]
Kersey, Kathryn [7 ]
Brainard, Diana M. [7 ]
Svarovskaia, Evguenia [7 ]
Mo, Hongmei [7 ]
Han, Kwang-Hyub [8 ]
Mizokami, Masashi [9 ]
Duan, Zhongping [10 ]
机构
[1] Peking Univ, Peoples Hosp, Hepatol Inst, Beijing Key Lab Hepatitis C & Immunol Liver Dis, Beijing, Peoples R China
[2] Yamanashi Prefectural Hosp Org, Yamanashi, Japan
[3] Univ Ulsan, Asan Med Ctr, Coll Med, Seoul, South Korea
[4] Shanghai Jiao Tong Univ, Ruijin Hosp, Shanghai, Peoples R China
[5] Southern Med Univ, Nanfang Hosp, Guangzhou, Guangdong, Peoples R China
[6] Capital Med Univ, Beijing Friendship Hosp, Beijing, Peoples R China
[7] Gilead Sci Inc, 353 Lakeside Dr, Foster City, CA 94404 USA
[8] Yonsei Univ, Coll Med, Seoul, South Korea
[9] Kohnodai Hosp, Natl Ctr Global Hlth & Med, Chiba, Japan
[10] Capital Med Univ, Beijing Youan Hosp, Beijing, Peoples R China
关键词
Direct-acting antivirals; Resistance associated substitutions; HEPATITIS-C VIRUS; GENOTYPE; 1-6; CLINICAL-TRIALS; SOFOSBUVIR; LEDIPASVIR/SOFOSBUVIR; INHIBITOR; VARIANTS;
D O I
10.1016/j.antiviral.2018.08.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background & aims: Resistance associated substitutions (RAS) can reduce the efficacy of some direct-acting antiviral HCV regimens. Here, prevalence of RAS in genotype (GT) 1b, 2, 3, and 6 HCV-infected patients from Asian counties, North America and Europe are described and compared. Methods: Pretreatment HCV RAS were assessed with 15% cutoff from patients enrolled in clinical trials of sofosbuvir-containing regimens in Mainland China, Japan, Korea, and India. Phylogenetic analyses were performed to investigating subtype diversity. Results: In GT1b patients, the prevalence of NS5A RAS, including Y93H, was similar across Asian countries (18-21%), and North America (15%) or Europe (19%). The prevalence of NS5B NI RAS, including L159F, was lower in Asian countries (1-5%) compared to North America (4%) or Europe (20%). The prevalence of NS3 RAS in patients from China (22%) and North America (28%) were lower than in Europe (40%). For GT2 patients in China, 100% had GT2a subtype with high prevalence of NS5A L31M. For GT3, the prevalence of GT3b was substantially higher in China (54%) than in North America or Europe (< 1%); 99% of GT3b patients in China had NS5A RAS A30K + L31M, which confers high levels of resistance to NS5A inhibitors. In GT3a patients in China, the prevalence of NS5A RAS was lower (5%) than in North America and Europe (14-16%). Prevalence of NS5B NI RAS in GT2 and GT3 patients was rare across regions (< 2%). Conclusions: Differences in the prevalence of GT2 and GT3 subtypes and NS5A RAS were observed between Asian and Western countries.
引用
收藏
页码:178 / 184
页数:7
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