Kawaoka Tomokazu, Imamura Michio, Morio Kei, Nakamura Yuki, Tsuge Masataka, Nelson Hayes C, Kawakami Yoshiiku, Aikata Hiroshi, Ochi Hidenori, Ishiyama Kouhei, Ide Kentaro, Tashiro Hirotaka, Ohdan Hideki, Chayama Kazuaki
Department of Gastroenterology and Metabolism, Applied Life Sciences, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Liver Research Project Center, Hiroshima University, Hiroshima, Japan.
Hepatol Res. 2016 Jun;46(7):707-12. doi: 10.1111/hepr.12602. Epub 2015 Nov 2.
We previously reported our data on telaprevir or simeprevir used in combination with pegylated interferon (PEG IFN) and ribavirin (RBV) for the treatment of recurrent hepatitis C virus (HCV) genotype 1 infection after liver transplantation (LT). Here, we report three patients who achieved viral responses with no effect on the blood concentrations of immunosuppressive agents following daclatasvir and asunaprevir treatment. The first patient was a 57-year-old man with HCV-related liver cirrhosis who failed to respond to PEG IFN/RBV after living donor LT. He had been treated with 1 mg/day of tacrolimus. The second was a 63-year-old man with HCV-related liver cirrhosis and hepatocellular carcinoma who failed to respond to PEG IFN/RBV after living donor LT. He had been treated with 1 mg/day of tacrolimus. The third was a 61-year-old man with HCV-related liver cirrhosis. He had been treated with mycophenolate mofetil (MMF). Serum HCV RNA became undetectable by TaqMan polymerase chain reaction test after 4 weeks of daclatasvir and asunaprevir treatment in all patients, and no remarkable fluctuations in blood concentration were observed either in tacrolimus or in MMF during 24 weeks of therapy. No adverse events were observed, and all patients received the full dose of daclatasvir and asunaprevir over 24 weeks. Serum HCV RNA remained negative at 12 weeks after the end of treatment in all patients. The daclatasvir and asunaprevir treatment showed a remarkable viral response with little effect on blood levels of immunosuppressive agents for recurrent HCV genotype 1 infection after LT.
我们之前报告了关于特拉匹韦或simeprevir联合聚乙二醇干扰素(PEG IFN)和利巴韦林(RBV)用于治疗肝移植(LT)后复发的丙型肝炎病毒(HCV)1型感染的数据。在此,我们报告3例患者,他们在接受达卡他韦和阿舒瑞韦治疗后实现了病毒学应答,且对免疫抑制剂的血药浓度没有影响。首例患者为一名57岁男性,患有HCV相关肝硬化,活体供肝LT后对PEG IFN/RBV治疗无应答。他一直接受每日1毫克他克莫司治疗。第二例是一名63岁男性,患有HCV相关肝硬化和肝细胞癌,活体供肝LT后对PEG IFN/RBV治疗无应答。他一直接受每日1毫克他克莫司治疗。第三例是一名61岁男性,患有HCV相关肝硬化。他一直接受霉酚酸酯(MMF)治疗。所有患者在接受达卡他韦和阿舒瑞韦治疗4周后,TaqMan聚合酶链反应检测显示血清HCV RNA不可检测,且在24周治疗期间他克莫司或MMF的血药浓度均未观察到明显波动。未观察到不良事件,所有患者在24周内均接受了全剂量的达卡他韦和阿舒瑞韦治疗。所有患者在治疗结束后12周时血清HCV RNA仍为阴性。达卡他韦和阿舒瑞韦治疗对LT后复发的HCV 1型感染显示出显著的病毒学应答,且对免疫抑制剂的血药水平影响很小。