Akuta Norio, Suzuki Fumitaka, Sezaki Hitomi, Suzuki Yoshiyuki, Hosaka Tetsuya, Someya Takashi, Kobayashi Masahiro, Saitoh Satoshi, Watahiki Sachiyo, Sato Junko, Matsuda Marie, Kobayashi Mariko, Arase Yasuji, Ikeda Kenji, Kumada Hiromitsu
Department of Gastroenterology, Toranomon Hospital, Tokyo, Japan.
Intervirology. 2005;48(6):372-80. doi: 10.1159/000086064.
Patients with high titer (>/=100 kIU/ml) of hepatitis C virus (HCV) genotype 1b do not achieve highly sustained virological response rates to combination therapy with interferon plus ribavirin. Non-virological responders (NVRs, namely ultimate resistant cases) who do not achieve HCV-RNA negativity during treatment are also encountered. We investigated the pretreatment virological features of NVRs.
We evaluated 50 consecutive Japanese adults with high titer of HCV genotype 1b who received combination therapy for 48 weeks. We investigated the pretreatment substitution patterns in amino acids 1-191 of the core region and amino acids 2209-2248 of NS5A, and early viral kinetics.
Overall, a non-virological response was noted in 12 (24%) patients. Multivariate analysis identified serum albumin <3.9 g/dl, substitutions of amino acid 70 in the core region, and substitutions of amino acid 91 as independent and significant factors associated with a non-virological response. Especially, substitutions of arginine (R) by glutamine (Q) at amino acid 70, and/or leucine (L) by methionine (M) at amino acid 91 were significantly more common in NVRs. The falls in HCV-RNA levels during treatment in patients with specific substitutions in the core region were significantly less than in those without such substitutions.
Our results suggest that serum albumin and amino acid substitution patterns in the core region in patients with high titers of HCV genotype 1b may have an effect on combination therapy in NVRs. Further large-scale studies are required to examine the role of amino acid substitutions specific to a non-virological response to combination therapy.
丙型肝炎病毒(HCV)1b基因型高滴度(≥100 kIU/ml)的患者接受干扰素联合利巴韦林的联合治疗时,无法实现高持续病毒学应答率。在治疗期间未实现HCV-RNA阴性的非病毒学应答者(NVRs,即最终耐药病例)也很常见。我们研究了NVRs的治疗前病毒学特征。
我们评估了50例连续接受48周联合治疗的日本成年HCV 1b基因型高滴度患者。我们研究了核心区1-191位氨基酸和NS5A的2209-2248位氨基酸的治疗前替代模式,以及早期病毒动力学。
总体而言,12例(24%)患者出现非病毒学应答。多变量分析确定血清白蛋白<3.9 g/dl、核心区70位氨基酸替代以及91位氨基酸替代是与非病毒学应答相关的独立且显著的因素。特别是,NVRs中70位氨基酸处精氨酸(R)被谷氨酰胺(Q)替代,和/或91位氨基酸处亮氨酸(L)被蛋氨酸(M)替代的情况明显更常见。核心区有特定替代的患者在治疗期间HCV-RNA水平的下降明显低于无此类替代的患者。
我们的结果表明,HCV 1b基因型高滴度患者的血清白蛋白和核心区氨基酸替代模式可能对NVRs的联合治疗有影响。需要进一步的大规模研究来检验联合治疗非病毒学应答特有的氨基酸替代的作用。