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移植受者中的丙型肝炎感染。

Hepatitis C infection in the transplant recipient.

作者信息

Terrault N A, Wright T L, Pereira B J

机构信息

University of California, San Francisco, USA.

出版信息

Infect Dis Clin North Am. 1995 Dec;9(4):943-64.

PMID:8747774
Abstract

This article highlights the increasing role of HCV in the transplant setting. Its importance in the liver transplant setting is clear. It produces end-stage liver disease and represents a common indication for transplant referral. Recurrent infection is nearly universal posttransplant in those with viremia pretransplant. Acquired disease is uncommon. The natural history of posttransplant disease suggests there is no significant impact of graft or patient survival, at least in the short-term. Long-term follow-up is needed, as well as more detailed study of the factors contributing to posttransplant disease. Kidney transplant patients commonly are infected with HCV prior to transplantation. Acquisition of infection through infected donors also serves as a source of HCV infection. HCV infection after transplantation is associated with an increased risk of liver disease but has no significant effect on short-term patient survival. The issues of organ allocation from anti-HCV-positive donors are particularly relevant to this patient population because maintenance dialysis always is a treatment alternative to transplantation. Much less information is available on other transplant groups, such as heart, lung, and bone marrow transplant recipients. There are many unanswered questions, especially with respect to the natural history of disease after 5 to 10 years of infection. The pathogenesis of infection in the transplant setting is emerging slowly but requires further investigation. Both direct viral cytopathicity and host-mediated immunity appear to play a role in liver injury. An increased understanding of pathogenicity will lead to improved management of patients with HCV infection both pre- and posttransplant.

摘要

本文强调了丙型肝炎病毒(HCV)在移植领域中日益重要的作用。其在肝移植领域的重要性显而易见。它会导致终末期肝病,是移植转诊的常见指征。移植前存在病毒血症的患者移植后复发性感染几乎普遍存在。获得性疾病并不常见。移植后疾病的自然史表明,至少在短期内,对移植物或患者生存没有显著影响。需要进行长期随访,以及对导致移植后疾病的因素进行更详细的研究。肾移植患者在移植前通常已感染HCV。通过受感染供体获得感染也是HCV感染的一个来源。移植后HCV感染与肝病风险增加相关,但对患者短期生存没有显著影响。来自抗HCV阳性供体的器官分配问题与该患者群体尤其相关,因为维持性透析始终是移植的一种替代治疗方法。关于其他移植群体,如心脏、肺和骨髓移植受者的信息要少得多。有许多问题尚未得到解答,尤其是关于感染5至10年后疾病的自然史。移植环境中感染的发病机制正在缓慢显现,但需要进一步研究。直接病毒细胞病变和宿主介导的免疫似乎都在肝损伤中起作用。对发病机制的进一步了解将改善HCV感染患者移植前后的管理。

相似文献

1
Hepatitis C infection in the transplant recipient.移植受者中的丙型肝炎感染。
Infect Dis Clin North Am. 1995 Dec;9(4):943-64.
2
Hepatitis C virus infection and organ transplantation.丙型肝炎病毒感染与器官移植
Prog Liver Dis. 1993;11:215-30.
3
Hepatitis C virus and nonliver solid organ transplantation.丙型肝炎病毒与非肝脏实体器官移植。
Transplantation. 2013 Mar 27;95(6):779-86. doi: 10.1097/TP.0b013e318273fec4.
4
Fibrosing cholestatic hepatitis in renal transplant recipients with hepatitis C virus infection.丙型肝炎病毒感染的肾移植受者中的纤维化胆汁淤积性肝炎
Liver Transpl Surg. 1999 Jul;5(4):294-300. doi: 10.1002/lt.500050417.
5
Factors influencing renal function after liver transplantation. Results from the MOST, an international observational study.肝移植后影响肾功能的因素。国际观察性研究MOST的结果。
Dig Liver Dis. 2009 May;41(5):350-6. doi: 10.1016/j.dld.2008.09.018. Epub 2008 Nov 28.
6
Liver transplant for hepatitis C virus: effect of using older donor grafts on short- and medium-term survival.丙型肝炎病毒的肝移植:使用较老供体移植物对短期和中期生存的影响。
Arch Surg. 2008 Jul;143(7):679-85; discussion 685. doi: 10.1001/archsurg.143.7.679.
7
Transplantation of kidneys from HCV-positive donors: a safe strategy?来自丙型肝炎病毒阳性供体的肾脏移植:一种安全的策略?
J Nephrol. 2003 Sep-Oct;16(5):617-25.
8
[Treatment of recurrent HCV infection after liver transplantation].肝移植后复发性丙型肝炎病毒感染的治疗
Acta Med Croatica. 2005;59(5):443-6.
9
Hepatitis C infection and the patient with end-stage renal disease.丙型肝炎感染与终末期肾病患者
Hepatology. 2002 Jul;36(1):3-10. doi: 10.1053/jhep.2002.34613.
10
Hepatitis C virus infection in liver allografts.肝移植受者中的丙型肝炎病毒感染。
Pathol Annu. 1995;30 Pt 2:203-26.

引用本文的文献

1
Infections in solid-organ transplant recipients.实体器官移植受者的感染
Clin Microbiol Rev. 1997 Jan;10(1):86-124. doi: 10.1128/CMR.10.1.86.