Andonov Anton, Kadkhoda Kamran, Osiowy Carla, Kaita Kelly
Public Health Agency of Canada, National Microbiology Laboratory, Winnipeg, Manitoba, Canada.
Can J Gastroenterol. 2013 Jul;27(7):414-6. doi: 10.1155/2013/273856.
Traditional therapy with pegylated interferon and ribavirin combined with the new protease inhibitors boceprevir or telaprevir has demonstrated improved outcomes in hepatitis C virus (HCV)-infected patients. Prevalence data regarding pre-existing drug-resistant variants to these two new virus inhibitors in the Canadian population are not available.
To detect pre-existing mutations conferring resistance to boceprevir and⁄or telaprevir in Canadian patients infected with HCV genotype 1a.
Resistance-associated mutations (RAMs) were evaluated in 85 patients infected with HCV genotype 1a who had not yet received antiviral therapy. The NS3 protease gene was sequenced and common RAMs were identified based on a recently published list.
The overall prevalence of pre-existing RAMs to boceprevir and telaprevir was higher compared with other similar studies. All of the observed RAMs were associated with a low level of resistance. A surprisingly high proportion of patients had the V55A RAM (10.6%). None of the mutations associated with a high level of resistance were observed. The simultaneous presence of two low-level resistance mutations (V36L and V55A) was observed in only one patient. Three other patients had both T54S RAM and V55I mutations, which may require a higher concentration of the protease drugs. The prevalence of various mutations in Aboriginal Canadian patients was higher (37.5%) compared with Caucasians (16.39%) (P=0.038).
The present study was the first to investigate pre-existing drug resistance to boceprevir⁄telaprevir in Canadian HCV-infected patients. A relatively high proportion of untreated HCV genotype 1a patients in Manitoba harbour low-level RAMs, especially patients of Aboriginal descent, which may contribute to an increased risk of treatment failure.
聚乙二醇化干扰素和利巴韦林联合新型蛋白酶抑制剂博赛匹韦或特拉匹韦的传统疗法已证明可改善丙型肝炎病毒(HCV)感染患者的治疗效果。加拿大人群中针对这两种新型病毒抑制剂的预先存在的耐药变异体的流行数据尚不可得。
检测加拿大感染HCV 1a基因型患者中预先存在的对博赛匹韦和/或特拉匹韦耐药的突变。
对85例尚未接受抗病毒治疗的HCV 1a基因型感染患者的耐药相关突变(RAMs)进行评估。对NS3蛋白酶基因进行测序,并根据最近公布的列表鉴定常见的RAMs。
与其他类似研究相比,预先存在的对博赛匹韦和特拉匹韦耐药的RAMs总体患病率更高。所有观察到的RAMs均与低水平耐药相关。令人惊讶的是,有相当高比例的患者存在V55A突变(10.6%)。未观察到与高水平耐药相关的突变。仅在1例患者中观察到两个低水平耐药突变(V36L和V55A)同时存在。另外3例患者同时存在T54S突变和V55I突变,这可能需要更高浓度的蛋白酶药物。加拿大原住民患者中各种突变的患病率(37.5%)高于白种人(16.39%)(P = 0.038)。
本研究首次调查了加拿大HCV感染患者中预先存在的对博赛匹韦/特拉匹韦的耐药情况。马尼托巴省未经治疗的HCV 1a基因型患者中,相当高比例携带低水平的RAMs,尤其是原住民后裔患者,这可能会增加治疗失败的风险。