Division of Hepatology, Department of Hepatobiliary Sciences and Liver Transplantation, King Abdulaziz Medical City and King Saud bin Abdulaziz University for Health Sciences, National Guard Health Affairs, Riyadh 11324, Saudi Arabia.
World J Gastroenterol. 2012 Jan 7;18(1):55-63. doi: 10.3748/wjg.v18.i1.55.
To assess the efficacy and safety of combined pegylated interferon and ribavirin therapy in hepatitis C virus (HCV) infection in renal transplant recipients.
This is a retrospective chart review of post renal transplant patients who were positive for anti-HCV and HCV-RNA, and who have received treatment with combination of pegylated interferon and ribavirin between October 2003 and December 2008. Only patients with stable graft function and absence of evidence of cirrhosis and who received the therapy for continuous 48 wk were included. Nineteen patients (13 male and 6 female) were identified and included. The patient's complete blood count, liver and kidney profile, and calculated glomerular filtration rate (GFR) were monitored every 6-8 wk while on treatment. HCV-RNA was tested at 12 wk for early virological response, at 48 wk for end of treatment response (ETR), and then retested at 24, and 48 wk after completion of therapy for sustained virological response (SVR). Liver biopsies were obtained before treatment from all patients and graft kidney biopsies were performed as required.
Of the entire cohort, 9 patients (47.4%) showed an ETR and 8 had SVR (42.1%). Of the 8 patients with abnormal alanine aminotransferase (ALT) levels at baseline, 78.9% had their ALT normalized (including the virological non responders). ALT was normal in all responders at the end of therapy and at 24 wk post therapy (100%). Only one patient (5.3%) developed an increase in creatinine and decline in GFR from baseline towards the end of treatment. This patient's kidney biopsy revealed borderline rejection. There was no impact on response by HCV-genotype, initial HCV RNA load, age or sex of the patient or duration post transplant before commencement of therapy. All patients tolerated treatment in the same way as non-transplant with no unusual or increased occurrence of side effects.
The combination of pegylated interferon and ribavirin is effective in suppressing HCV-RNA, with a low risk of graft rejection or failure in HCV infected renal transplant recipients.
评估聚乙二醇干扰素联合利巴韦林治疗肾移植受者丙型肝炎病毒(HCV)感染的疗效和安全性。
这是一项回顾性病历分析,纳入了 2003 年 10 月至 2008 年 12 月期间接受聚乙二醇干扰素联合利巴韦林治疗的抗-HCV 和 HCV-RNA 阳性的肾移植后患者。仅纳入了移植肾功能稳定且无肝硬化证据并接受了 48 周连续治疗的患者。共确定并纳入了 19 例患者(13 名男性和 6 名女性)。治疗期间每 6-8 周监测患者的全血细胞计数、肝肾功能和计算肾小球滤过率(GFR)。在治疗 12 周时检测 HCV-RNA 以评估早期病毒学应答,在治疗结束时检测 48 周时评估治疗结束应答(ETR),然后在完成治疗后 24 周和 48 周时检测持续病毒学应答(SVR)。所有患者在治疗前均进行了肝活检,根据需要进行了移植物肾活检。
整个队列中,9 例(47.4%)患者出现 ETR,8 例患者(42.1%)出现 SVR。在基线时丙氨酸氨基转移酶(ALT)水平异常的 8 例患者中,78.9%的患者 ALT 正常(包括病毒学无应答者)。所有应答者在治疗结束时和治疗后 24 周时的 ALT 均正常(100%)。只有 1 例患者(5.3%)在治疗结束时出现肌酐升高和 GFR 从基线下降。该患者的肾活检显示边缘性排斥。HCV 基因型、初始 HCV RNA 载量、患者年龄或性别或开始治疗前的移植后时间对反应无影响。所有患者的治疗耐受性与非移植患者相同,无不良反应的发生率增加或不常见。
聚乙二醇干扰素联合利巴韦林可有效抑制 HCV-RNA,在 HCV 感染的肾移植受者中,发生移植物排斥或衰竭的风险较低。