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Sofosbuvir and Daclatasvir Combination Therapy in a Liver Transplant Recipient With Severe Recurrent Cholestatic Hepatitis C

机译:sofosbuvir和Daclatasvir联合治疗肝移植受者严重复发性胆汁淤积性丙型肝炎

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摘要

Recurrent HCV infection following liver transplantation can lead to accelerated allograft injury that is difficult to treat with interferon. The aim of this study is to describe the first ever use of an interferon‐free, all oral regimen in a liver transplant recipient with severe recurrent HCV. A 54‐year‐old male with HCV genotype 1b developed severe cholestatic HCV at 6 months posttransplant with ascites, AST 503 IU/mL, alkaline phosphatase of 298 IU/mL, HCV RNA of 12 000 000 IU/mL, and histological cholestasis with pericellular fibrosis. Sofosbuvir, an HCV polymerase inhibitor (400 mg/day), and daclatasvir, an HCV NS5A replication complex inhibitor (60 mg/day), were co‐administered for 24 weeks. Within 4 weeks of initiating treatment, serum HCV RNA levels became undetectable and liver biochemistries normalized with concomitant resolution of ascites. The patient achieved a sustained virological response with undetectable HCV RNA at 9 months posttreatment. During and following treatment, the daily dose and blood level of tacrolimus remained stable and unchanged. The rapid and sustained suppression of HCV replication in this liver transplant recipient provides great promise for the use of combination oral antiviral regimens in other immunosuppressed and interferon refractory HCV patients. A patient with severe cholestatic hepatitis C virus genotype 1b infection at nine months after liver transplantation was successfully treated with a six‐month course of oral sofosbuvir in combination with daclatasvir and remains HCV RNA negative during posttreatment follow‐up with improved liver biochemistries and health.
机译:肝移植后HCV的反复感染可导致同种异体移植物加速损伤,很难用干扰素治疗。这项研究的目的是描述有严重HCV复发的肝移植受者首次使用无干扰素的全口服方案。一名54岁的HCV基因型1b的男性在移植后6个月出现严重的胆汁淤积性HCV,伴有腹水,AST 503 / IU / mL,碱性磷酸酶298 IU / mL,HCV RNA 12 000 000 IU / mL和组织学性胆汁淤积细胞周纤维化。 HCV聚合酶抑制剂Sofosbuvir(400μmg/天)和HCV NS5A复制复合物抑制剂daclatasvir(60μmg/天)并用24周。在开始治疗的4周内,无法检测到血清HCV RNA水平,并且伴随腹水消退,肝生物化学正常化。患者在治疗后9个月使用未检测到的HCV RNA获得了持续的病毒学应答。在治疗期间和之后,他克莫司的日剂量和血药水平保持稳定且未发生变化。在该肝移植受者中,HCV复制的快速和持续抑制为在其他免疫抑制和干扰素难治性HCV患者中联合使用口服抗病毒方案提供了广阔前景。肝移植后9个月有严重的胆汁淤积性丙型肝炎病毒基因1b感染的患者成功接受了六个月疗程的口服sofosbuvir联合daclatasvir的治疗,并且在治疗后的随访期间HCV RNA阴性,从而改善了肝脏的生物化学和健康。

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