Hepatitis B virus infection after renal transplantation in the presence of antibody to hepatitis B surface antigen immunity

被引:16
作者
Kim, KH
Ahn, SH
Chung, HY
Paik, YH
Lee, KS
Kim, YS
Chon, CY
Moon, YM
Han, KH
机构
[1] Yonsei Univ, Coll Med, Dept Internal Med, Seoul 120752, South Korea
[2] Yonsei Med Res Ctr, Seoul, South Korea
[3] Brain Korea 21 Project Med Sci, Seoul, South Korea
[4] Yonsei Univ, Coll Med, Dept Surg, Inst Gastroenterol, Seoul 120752, South Korea
关键词
'a' determinant mutants; antibody to hepatitis B surface antigen immunity; hepatitis B virus infection; renal transplantation;
D O I
10.1111/j.1440-1746.2003.03303.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aim: Hepatitis B virus (HBV) infection has been known to be hampered by immunity against hepatitis B surface antigen (HBsAg). However, HBV with mutations within the common antigenic epitope of HBsAg, the 'a' determinant region, can escape from humoral immunity. Moreover, HBV infection by 'a' determinant mutants in chronic HBV patients has been reported after renal transplantation. In the present study, the authors investigated HBV infection after renal transplantation despite passive immunization or resolved HBV infection. Methods: A total of 1682 patients who underwent a renal transplant between 1979 and 1998 at the Severance Hospital, Yonsei University College of Medicine, Korea, were enrolled. The sequence of the HBV genome was analyzed from two patients with antibody to HBsAg (anti-HBs) immunity. Results: Of 1682 patients who were HBsAg negative before transplantation, 21 patients were found to be HBsAg positive, with elevated aspartate aminotransferase and alanine aminotransferase levels after transplantation. Interestingly, six of 21 (28.6%) patients were anti-HBs positive before the transplantation. Sequence analysis of the cloned HBV from two of six patients with anti-HBs immunity showed no evidence of significant mutations within the 'a' determinant region, suggesting a wild-type of HBV. Their donors were not exposed to HBV before transplantation (all HBV markers were negative). Seven deaths of 21 patients were ascribed to HBV-related complications. Conclusions: Regardless of anti-HBs immunity, HBV infection occurred in immunosuppressed patients in a high endemic area. The molecular mechanism and clinical impact of HBV infection after renal transplantation in patients with anti-HBs immunity should be further reappraised. (C) 2004 Blackwell Publishing Asia Pty Ltd.
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收藏
页码:847 / 853
页数:7
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