干扰素诱导/干扰素α 2b联合利巴韦林治疗慢性丙型肝炎患者

K I Kim, N Sasase, M Taniguchi, K Mita, K Kinoshita, T Togitani, M Shikata, N Kimura, S Izawa, A Ohtani, K Nakao, Y Muramoto, S R Kim, S Nabeshima, F Ishii, K Tanaka, Y Hayashi
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引用次数: 0

摘要

用干扰素(IFN)和利巴韦林治疗慢性丙型肝炎病毒(HCV)感染,可使基因型1b和高病毒载量患者的病毒根除率提高不到20%。在这项研究中,我们评估了ifn - β诱导/IFN-alpha2b联合利巴韦林是否能增强慢性丙型肝炎患者的治疗效果。在14例HCV-RNA高水平(> 100 K/U/ml)患者中,比较了ifn - β诱导/IFN-alpha2b联合利巴韦林治疗(A组,n=7)与IFN-alpha2b联合利巴韦林治疗(B组,n=7)的疗效。两组(分别为A组和B组)在治疗开始后2周(0%和14.3%)、治疗结束时(71.4%和100%)和治疗结束后6个月(28.6%和14.3%)的HCV-RNA清除率均无显著差异。A组和B组完全恢复者分别为28.6%和14.3%,短暂恢复者分别为42.9%和85.7%,无恢复者分别为28.6%和0%。治疗2周后,A组和B组病毒载量的早期log变化分别为2.41 +/- 0.91和2.77 +/- 0.20,两组之间无显著差异。在本研究中,我们无法证明ifn - β诱导/IFN-alpha2b +利巴韦林治疗在基因型1b和高病毒载量的患者中优于IFN-alpha2b +利巴韦林治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interferon-beta induction/interferon-alpha2b plus ribavirin therapy in patients with chronic hepatitis C.

Treatment of chronic hepatitis C virus (HCV) infection with interferon (IFN) and ribavirin improves the rate of eradication of the virus by less than 20% in patients with genotype 1b and a high viral load. In this study we assessed whether IFN-beta induction/IFN-alpha2b plus ribavirin enhances the efficacy of the therapy in patients with chronic hepatitis C. The efficacy of IFN-beta induction/IFN-alpha2b plus ribavirin therapy (group A, n=7) was compared with that of IFN-alpha2b plus ribavirin (group B, n=7) in 14 patients with high levels of HCV-RNA (> 100 K/U/ml). No significant differences were observed in the clearance of HCV-RNA between the two groups (A and B, respectively) 2 weeks after the start of the treatment (0% and 14.3%), at the end of the treatment (71.4% and 100%) and 6 months after the end of the treatment (28.6% and 14.3%). Recovery was complete in 28.6% and 14.3%, transient in 42.9% and 85.7% and absent in 28.6% and 0% in groups A and B, respectively. Early log changes in the viral load from the baseline after 2 weeks of treatment were 2.41 +/- 0.91 and 2.77 +/- 0.20 in groups A and B, respectively, with no significant difference between the two groups. In the present study, we were not able to demonstrate that IFN-beta induction/IFN-alpha2b plus ribavirin therapy was superior to IFN-alpha2b plus ribavirin therapy in patients with genotype 1b and high viral loads.

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