Orita Noriaki, Shimakami Tetsuro, Sunagozaka Hajime, Horii Rika, Nio Kouki, Terashima Tekeshi, Iida Noriho, Kitahara Masaaki, Takatori Hajime, Kawaguchi Kazunori, Kitamura Kazuya, Arai Kuniaki, Yamashita Taro, Sakai Yoshio, Yamashita Tatsuya, Mizukoshi Eishiro, Honda Masao, Kaneko Shuichi
Department of Gastroenterology, Kanazawa University Hospital, Kanazawa University Graduate School of Medical Science, 13-1 Takaramachi, Kanazawa, Ishikawa, 920-8641, Japan.
Clin J Gastroenterol. 2019 Feb;12(1):63-70. doi: 10.1007/s12328-018-0884-y. Epub 2018 Jul 11.
We report three cases of genotype 1b hepatitis C virus (HCV) reinfection after liver transplantation. When antiviral treatment was considered, all three patients had renal dysfunction and had been treated with immunosuppressive agents for a long time; one with tacrolimus (TAC) and the others with cyclosporine A (CyA). Therefore, the possible antiviral regimens among direct-acting antivirals (DAA) were limited and so we treated all three patients with ombitasvir/paritaprevir/ritonavir (OBV/PTV/r). Because ritonavir is known to markedly increase the blood concentration of TAC and CyA through drug-drug interactions, close monitoring of blood concentrations of TAC or CyA and dose adjustments of immunosuppressive agents were needed. Sustained virus response was achieved in all the patients treated, and there were no adverse effects or transplant rejection. OBV/PTV/r might be a useful DAA regimen for patients with genotype 1 HCV reinfection in the setting of renal dysfunction.
我们报告了3例肝移植后1b型丙型肝炎病毒(HCV)再感染的病例。考虑进行抗病毒治疗时,所有3例患者均存在肾功能不全,且长期接受免疫抑制剂治疗;1例使用他克莫司(TAC),其余2例使用环孢素A(CyA)。因此,直接抗病毒药物(DAA)中可能的抗病毒方案有限,所以我们用奥比他韦/帕利哌韦/利托那韦(OBV/PTV/r)治疗了所有3例患者。由于已知利托那韦通过药物相互作用可显著提高TAC和CyA的血药浓度,因此需要密切监测TAC或CyA的血药浓度并调整免疫抑制剂的剂量。所有接受治疗的患者均实现了持续病毒学应答,且未出现不良反应或移植排斥反应。对于肾功能不全情况下1型HCV再感染的患者,OBV/PTV/r可能是一种有用的DAA方案。