Achievement of Sustained Viral Response after Switching Treatment from Pegylated Interferon alpha-2b to alpha-2a and Ribavirin in Patients with Recurrence of Hepatitis C Virus Genotype 1 Infection after Liver Transplantation : A Case Report

Achievement of Sustained Viral Response after Switching Treatment from Pegylated Interferon alpha-2b to alpha-2a and Ribavirin in Patients with Recurrence of Hepatitis C Virus Genotype 1 Infection after Liver Transplantation : A Case Report
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肝移植后丙型肝炎病毒基因型 1 感染复发患者从聚乙二醇干扰素 α-2b 转为 α-2a 和利巴韦林治疗后获得持续病毒缓解:病例报告

DOI:
10.1159/000328661
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发表时间:
2011
期刊:
Intervirology (Elpub 25 Aug.)
影响因子:
--
通讯作者:
Chayama K
Chayama K
中科院分区:
--
文献类型:
--
作者:
Kawaoka T;Hiraga N;Takahashi S;Takaki S;Tsuge M;Nagaoki Y;Hashimoto Y;Katamura Y;Muki D;Hiramatsu A;Waki K;Imamura M;Kawakami Y;Aikata H;Ochi H;Tashiro H;Ohdan H;Chayama K

文献摘要

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我们报告了一例活体肝移植术后丙型肝炎病毒(HCV)感染复发的患者,在从聚乙二醇干扰素(PEG-IFN)α-2b转换为α-2a和利巴韦林(RBV)治疗后获得持续病毒应答的病例。患者是一名62岁男性,因HCV基因型1b感染而患有肝硬化。该患者在干扰素敏感性决定区有8个氨基酸(aa)取代,在核心区分别在aa 70和aa 91处有突变型和野生型取代。该患者具有次要基因型(GG)IL 28 B单核苷酸多态性(rs 8099917)。他最初接受干扰素α-2b和RBV治疗2年,后来发展为肝细胞癌(HCC)。在手术切除HCC后,他随后接受PEG-IFN α-2b和RBV治疗1.5年,在治疗过程中没有检测到病毒血症。由于HCC复发,患者接受了活体肝移植。后来,丙型肝炎复发。为了控制复发,他接受了另一个疗程的PEG-IFN α-2b和RBV。然而,发生了突破性病毒血症。因此,PEG-IFN从α-2b转换为α-2a和RBV,持续17个月。患者最终获得了持续的病毒应答。
We report a case in which sustained viral response was achieved after switching treatment from pegylated interferon (PEG-IFN) α-2b to α-2a and ribavirin (RBV) in patients with recurrence of hepatitis C virus (HCV) infection after living donor liver transplantation. The patient was a 62-year-old man with liver cirrhosis due to HCV genotype 1b infection. The patient had 8 amino acid (aa) substitutions in the interferon sensitivity-determining region, and had substitutions for mutant and wild-type at aa70 and aa91, respectively, in the core region. The patient had minor genotype (GG)IL28Bsingle nucleotide polymorphisms (rs8099917). He had initially received interferon α-2b and RBV for 2 years, and later developed hepatocellular carcinoma (HCC). After surgical resection of HCC, he subsequently received PEG-IFN α-2b and RBV for 1.5 years, without undetectable viremia during the treatment course. Due to recurrence of HCC, the patient received a living donor liver transplantation. Later on, hepatitis C relapsed. For the management of relapse, he received another course of PEG-IFN α-2b and RBV. However, breakthrough viremia occurred. PEG-IFN was thus switched from α-2b to α-2a and RBV for another 17 months. The patient eventually achieved a sustained viral response.