Current therapeutic strategies for recurrent hepatitis B virus infection after liver transplantation

被引:15
作者
Jiang, Li [1 ]
Yan, Lu-Nan [1 ]
机构
[1] Sichuan Univ, W China Hosp, Dept Liver & Vasc Surg, Liver Transplantat Ctr, Chengdu 610041, Sichuan Prov, Peoples R China
关键词
Therapy; Hepatitis B virus; Recurrent hepatitis B virus infection; Antiviral drugs; Liver transplantation; ADEFOVIR DIPIVOXIL THERAPY; TENOFOVIR DISOPROXIL FUMARATE; ANTIGEN-POSITIVE PATIENTS; IN-VITRO SUSCEPTIBILITY; LAMIVUDINE THERAPY; DE-NOVO; IMMUNE GLOBULIN; ENTECAVIR RESISTANCE; POLYMERASE MUTATIONS; FOLLOW-UP;
D O I
10.3748/wjg.v16.i20.2468
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatitis B virus (HBV)-related liver disease is the leading indication for liver transplantation (LT) in Asia, especially in China. With the introduction of hepatitis B immunoglobulin (HBIG) and oral antiviral drugs, the recurrent HBV infection rate after LT has been evidently reduced. However, complete eradication of recurrent HBV infection after LT is almost impossible. Recurrent graft infection may lead to rapid disease progression and is a frequent cause of death within the first year after LT. At present, the availability of new oral medications, especially nucleoside or nucleotide analogues such as adefovir dipivoxil, entecavir and tenofovir disoproxil fumarate, further strengthens our ability to treat recurrent HBV infection after LT. Moreover, since combined treatment with HBIG and antiviral agents after liver re-transplantation may play an important role in improving the prognosis of recurrent HBV infection, irreversible graft dysfunction secondary to recurrent HBV infection in spite of oral medications should no longer be considered an absolute contraindication for liver re-transplantation. Published reviews focusing on the therapeutic strategies for recurrent HBV infection after LT are very limited. In this article, the current therapeutic strategies for recurrent HBV infection after LT and evolving new trends are reviewed to guide clinical doctors to choose an optimal treatment plan in different clinical settings. (C) 2010 Baishideng. All rights reserved.
引用
收藏
页码:2468 / 2475
页数:8
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