Ueda Eri, Enomoto Nobuyuki, Sakamoto Naoya, Hamano Kosei, Sato Chifumi, Izumi Namiki, Watanabe Mamoru
Department of Gastroenterology and Hepatology, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan.
Hepatol Res. 2004 Jun;29(2):89-96. doi: 10.1016/j.hepres.2004.02.014.
Treatment of chronic hepatitis C virus (HCV) infection with interferon (IFN) and ribavirin improves the rate of eradication of HCV, but only about 13-14% of non-responders (NR) with HCV of genotype 1b previously treated with IFN achieve a sustained virological response (SVR). To determine whether HCV quasispecies diversity correlates with the outcome of therapy with IFN and ribavirin, we studied 13 patients undergoing combination therapy with IFN-alpha2b and ribavirin after failure of IFN monotherapy. HCV quasispecies diversity was assessed by cloning and sequencing before and during combination therapy. During therapy, quasispecies diversity diminished in NR patients, both in the hypervariable region (HVR) 1 of the envelope 2 (E2) domain and in the interferon sensitivity-determining region (ISDR) in the NS5A. Pre-treatment nucleotide quasispecies diversity was lower in SVR and end-of-therapy viral response (ETR) patients than in NR patients. Resistance to ribavirin was associated with high pre-treatment heterogeneity and the selection of quasispecies of the HCV genome. HVR quasispecies may be a predictor of efficacy of combination therapy with IFN and ribavirin.
用干扰素(IFN)和利巴韦林治疗慢性丙型肝炎病毒(HCV)感染可提高HCV的根除率,但先前接受过IFN治疗的1b型HCV无应答者(NR)中只有约13 - 14%能实现持续病毒学应答(SVR)。为了确定HCV准种多样性是否与IFN和利巴韦林治疗的结果相关,我们研究了13例在IFN单药治疗失败后接受IFN-α2b和利巴韦林联合治疗的患者。在联合治疗前和治疗期间,通过克隆和测序评估HCV准种多样性。治疗期间,NR患者的准种多样性在包膜2(E2)结构域的高变区(HVR)1和NS5A中的干扰素敏感性决定区(ISDR)均有所降低。SVR和治疗结束时病毒应答(ETR)患者治疗前的核苷酸准种多样性低于NR患者。对利巴韦林的耐药性与治疗前的高异质性以及HCV基因组准种的选择有关。HVR准种可能是IFN和利巴韦林联合治疗疗效的预测指标。