Grassi Alberto, Ballardini Giorgio
Alberto Grassi, Giorgio Ballardini, Internal Medicine and Hepatology Division, Department of Internal Medicine, "Infermi" Hospital, 47923 Rimini, Italy.
World J Gastroenterol. 2014 Aug 28;20(32):11095-115. doi: 10.3748/wjg.v20.i32.11095.
Hepatitis C virus (HCV)-related cirrhosis represents the leading cause of liver transplantation in developed, Western and Eastern countries. Unfortunately, liver transplantation does not cure recipient HCV infection: reinfection universally occurs and disease progression is faster after liver transplant. In this review we focus on what happens throughout the peri-transplant phase and in the first 6-12 mo after transplantation: during this crucial period a completely new balance between HCV, liver graft, the recipient's immune response and anti-rejection therapy is achieved that will deeply affect subsequent outcomes. Nearly all patients show an early graft reinfection, with HCV viremia reaching and exceeding pre-transplant levels; in this setting, histological assessment is essential to differentiate recurrent hepatitis C from acute or chronic rejection; however, differentiating the two patterns remains difficult. The host immune response (mainly cellular mediated) appears to be crucial both in the control of HCV infection and in the genesis of rejection, and it is also strongly influenced by immunosuppressive treatment. At present no clear immunosuppressive strategy could be strongly recommended in HCV-positive recipients to prevent HCV recurrence, even immunotherapy appears to be ineffective. Nonetheless it seems reasonable that episodes of rejection and over-immunosuppression are more likely to enhance the risk of HCV recurrence through immunological mechanisms. Both complete prevention of rejection and optimization of immunosuppression should represent the main goals towards reducing the rate of graft HCV reinfection. In conclusion, post-transplant HCV recurrence remains an unresolved, thorny problem because many factors remain obscure and need to be better determined.
丙型肝炎病毒(HCV)相关肝硬化是发达国家、西方国家和东方国家肝移植的主要原因。不幸的是,肝移植并不能治愈受者的HCV感染:普遍会发生再次感染,且肝移植后疾病进展更快。在本综述中,我们关注肝移植围手术期及移植后最初6 - 12个月内发生的情况:在这个关键时期,HCV、肝移植物、受者免疫反应和抗排斥治疗之间会达成一种全新的平衡,这将深刻影响后续结果。几乎所有患者都会出现早期移植物再次感染,HCV病毒血症达到并超过移植前水平;在这种情况下,组织学评估对于区分复发性丙型肝炎与急性或慢性排斥反应至关重要;然而,区分这两种模式仍然困难。宿主免疫反应(主要是细胞介导的)在控制HCV感染和排斥反应的发生中似乎都至关重要,并且它也受到免疫抑制治疗的强烈影响。目前,对于HCV阳性受者,尚无明确的免疫抑制策略可被强烈推荐用于预防HCV复发,甚至免疫治疗似乎也无效。尽管如此,排斥反应发作和过度免疫抑制似乎更有可能通过免疫机制增加HCV复发的风险。完全预防排斥反应和优化免疫抑制都应成为降低移植物HCV再次感染率的主要目标。总之,移植后HCV复发仍然是一个未解决的棘手问题,因为许多因素仍不清楚,需要更好地确定。