Fabrizi F, Martin P, Ponticelli C
Division of Nephrology and Dialysis, Maggiore Hospital, IRCCS, Milano, Italy.
Am J Kidney Dis. 2001 Nov;38(5):919-34. doi: 10.1053/ajkd.2001.28576.
With the success of organ transplantation, liver disease has emerged as an important cause of morbidity and mortality of renal transplant (RT) recipients. Numerous studies performed during the 1990s have shown that hepatitis C virus (HCV) infection is the leading cause of chronic liver disease among RT recipients. The transmission of HCV by renal transplantation of a kidney from an HCV-infected organ donor has been shown unequivocally. Liver biopsy is essential in the evaluation of liver disease of RT recipients, and histological studies have shown that HCV-related liver disease after renal transplantation is progressive. The outcome of HCV-related liver disease is probably more aggressive in RT recipients than immunocompetent individuals. Various factors can affect the progression of HCV in the RT population: coinfection with hepatitis B virus, time of HCV acquisition, type of immunosuppressive treatment, and concomitant alcohol abuse. The role of virological features of HCV remains unclear. The natural history of HCV infection after renal transplantation is under evaluation; however, recent surveys with long follow-ups have documented adverse effects of HCV infection on patient and graft survival in RT recipients. Use of renal grafts from HCV-infected donors in recipients with HCV infection does not appear to result in a greater burden of liver disease, at least for a short period. The association between HCV and de novo or recurrent glomerulonephritis after RT has been hypothesized and is an area of avid research. Reported studies do not support interferon (IFN) treatment for RT recipients with chronic hepatitis C because of the frequent occurrence of graft failure, and information on the use of other types of IFN or combined therapy (IFN plus ribavirin or amantadine) is not yet available in the RT population.
随着器官移植的成功,肝脏疾病已成为肾移植(RT)受者发病和死亡的重要原因。20世纪90年代进行的大量研究表明,丙型肝炎病毒(HCV)感染是RT受者慢性肝病的主要原因。已明确证实,来自HCV感染器官供体的肾脏进行肾移植可传播HCV。肝活检对于评估RT受者的肝脏疾病至关重要,组织学研究表明,肾移植后HCV相关肝病呈进行性发展。RT受者中HCV相关肝病的预后可能比免疫功能正常者更严重。多种因素可影响RT人群中HCV的进展:与乙型肝炎病毒合并感染、HCV感染时间、免疫抑制治疗类型以及同时存在的酒精滥用。HCV病毒学特征的作用仍不清楚。肾移植后HCV感染的自然史正在评估中;然而,近期长期随访调查记录了HCV感染对RT受者患者和移植物存活的不良影响。对于HCV感染的受者,使用来自HCV感染供体的肾移植物似乎不会导致更严重的肝脏疾病负担,至少在短期内如此。HCV与RT后新发或复发性肾小球肾炎之间的关联已被提出假设,是一个积极研究的领域。已报道的研究不支持对慢性丙型肝炎的RT受者使用干扰素(IFN)治疗,因为移植失败频繁发生,且关于RT人群中使用其他类型IFN或联合治疗(IFN加利巴韦林或金刚烷胺)的信息尚不可用。