Sprinzl Martin F, Otto Gerd, Galle Peter R, Schuchmann Marcus
Department of Internal Medicine, Johannes Gutenberg University Mainz, Mainz, Germany.
Clin Transplant. 2006;20 Suppl 17:117-23. doi: 10.1111/j.1399-0012.2006.00610.x.
Hepatitis C virus (HCV) re-infection of the liver graft has been recognized to be one of the most important factors that determines prognosis and outcome after liver transplantation in HCV-positive patients. Graft loss due to recurrent HCV re-cirrhosis and subsequent hepatic decompensation, which is the predominant cause of death among transplant recipients, reflects the prognostic significance of HCV re-infection. Despite better overall outcome after liver transplantation, the prognosis of HCV-infected patients has not improved during the last two decades. Recent data suggest that increased liver donor age and intensified immunosuppression of transplant patients are the most important contributors to this situation. Other prognostic factors need further confirmation to stratify risk constellations. As HCV cirrhosis has also become the leading indication for orthotopic liver transplantation, the therapeutic management of HCV re-infection is a central issue of liver transplantation. The antiviral approaches based on interferon (IFN) alpha and ribavirin combinations are still hampered by high toxicity and low efficacy. Sustained viral response rates are still as low as approximately 10-30% and further prospective clinical trials are mandatory to identify the best time point and schedule of antiviral treatment in transplant patients.
丙型肝炎病毒(HCV)对肝移植移植物的再感染已被认为是决定HCV阳性患者肝移植预后和结局的最重要因素之一。复发性HCV再发肝硬化及随后的肝功能失代偿导致的移植物丢失是移植受者死亡的主要原因,这反映了HCV再感染的预后意义。尽管肝移植后的总体结局有所改善,但在过去二十年中,HCV感染患者的预后并未得到改善。最近的数据表明,肝脏供体年龄增加和移植患者免疫抑制强化是导致这种情况的最重要因素。其他预后因素需要进一步证实,以对风险组合进行分层。由于HCV肝硬化也已成为原位肝移植的主要适应证,因此HCV再感染的治疗管理是肝移植的核心问题。基于α干扰素和利巴韦林联合使用的抗病毒方法仍然受到高毒性和低疗效的阻碍。持续病毒学应答率仍然低至约10%-30%,进一步的前瞻性临床试验对于确定移植患者抗病毒治疗的最佳时间点和方案是必不可少的。