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丙型肝炎病因所致的肝脏疾病与肝移植后早期急性排斥反应密切相关。

Hepatitis C etiology of liver disease is strongly associated with early acute rejection following liver transplantation.

作者信息

McTaggart Ryan A, Terrault Norah A, Vardanian Andrew J, Bostrom Alan, Feng Sandy

机构信息

Department of Surgery, Division of Transplantation, University of California San Francisco, San Francisco, CA 94143-0780, USA.

出版信息

Liver Transpl. 2004 Aug;10(8):975-85. doi: 10.1002/lt.20213.

Abstract

Although recurrent hepatitis C (HCV) occurs universally after liver transplantation (LT), its tempo and severity are variable and unpredictable. Diagnosis and treatment of early acute rejection (EAR) likely affect the course of recurrent HCV disease. We have studied a contemporary cohort of LT recipients to reexamine risk factors for EAR. We hypothesized that HCV etiology may represent a significant risk factor for EAR for many reasons. First, recurrent disease commonly causes biochemical abnormalities prompting allograft biopsy. Second, overlapping histologic features of acute rejection and recurrent HCV ambiguity may result in diagnostic ambiguity. Finally, the biology of hepatitis may precipitate an antidonor response in addition to an antiviral response. Records of 285 adult recipients undergoing primary LT for cirrhosis between January 1, 1999, and December 31, 2002, were retrospectively reviewed. EAR was defined as a biopsy-proven or an empirically treated episode within 6 months of LT. Cox proportional hazards analysis identified donor, recipient, transplant, and posttransplant characteristics associated with EAR; Kaplan-Meier analysis was used to assess rejection by etiology. HCV cirrhosis was the etiology for 51% of all LT recipients. There were 135 episodes of EAR (127 biopsy proven) in 117 recipients for an overall incidence of 41%. Patient groups with HCV and cholestatic / autoimmune disease groups exhibited the highest incidence of rejection at 49%. Recipient gender, ethnicity, etiology, LT year, and posttransplant immunosuppression levels were risk factors for EAR in univariate analysis; HCV etiology and female gender remained robust risk factors in multivariate analysis. Interferon-based therapy did not impact the incidence or timing of EAR. In conclusion, HCV etiology is strongly associated with EAR. HCV allograft reinfection may create an immunologic environment predisposed to EAR. Alternatively, the association of HCV and EAR may result from an increased frequency of allograft biopsy and may be further exacerbated by inability to accurately diagnose EAR in the setting of recurrent HCV.

摘要

尽管肝移植(LT)后复发性丙型肝炎(HCV)普遍发生,但其进展速度和严重程度各不相同且难以预测。早期急性排斥反应(EAR)的诊断和治疗可能会影响复发性HCV疾病的病程。我们研究了一组当代肝移植受者,以重新审视EAR的危险因素。我们假设HCV病因可能是EAR的一个重要危险因素,原因有很多。首先,复发性疾病通常会导致生化异常,从而促使进行同种异体移植活检。其次,急性排斥反应和复发性HCV的组织学特征重叠可能导致诊断模糊。最后,肝炎的生物学特性除了引发抗病毒反应外,还可能引发抗供体反应。回顾性分析了1999年1月1日至2002年12月31日期间285例因肝硬化接受初次肝移植的成年受者的记录。EAR定义为肝移植后6个月内经活检证实或经验性治疗的事件。Cox比例风险分析确定了与EAR相关的供体、受体、移植和移植后特征;采用Kaplan-Meier分析按病因评估排斥反应。HCV肝硬化是所有肝移植受者中51%的病因。117名受者发生了135次EAR事件(127次经活检证实),总发生率为41%。HCV患者组以及胆汁淤积/自身免疫性疾病组的排斥反应发生率最高,为49%。在单因素分析中,受者性别、种族、病因、肝移植年份和移植后免疫抑制水平是EAR的危险因素;在多因素分析中,HCV病因和女性性别仍然是可靠的危险因素。基于干扰素的治疗并未影响EAR的发生率或发生时间。总之,HCV病因与EAR密切相关。HCV同种异体移植再感染可能会创造一个易于发生EAR的免疫环境。或者,HCV与EAR的关联可能是由于同种异体移植活检频率增加所致,并且在复发性HCV的情况下,由于无法准确诊断EAR可能会进一步加剧这种关联。

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