Transmission of occult hepatitis B virus by transfusion to adult and pediatric recipients in Taiwan

被引:88
作者
Liu, CJ
Lo, SC
Kao, JH
Tseng, PT
Lai, MY
Ni, YH
Yeh, SH
Chen, PJ
Chen, DS
机构
[1] Natl Taiwan Univ, Coll Med, Grad Inst Clin Med, Taipei 100, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Internal Med, Div Gastroenterol, Taipei 100, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei 100, Taiwan
[4] Natl Taiwan Univ Hosp, Hepatitis Res Ctr, Taipei 100, Taiwan
[5] Natl Taiwan Univ Hosp, Dept Pediat, Taipei 100, Taiwan
[6] Natl Taiwan Univ Hosp, Dept Microbiol, Taipei 100, Taiwan
[7] Natl Taiwan Univ Hosp, Dept Med Res, Taipei 100, Taiwan
关键词
occult hepatitis B virus; transfusion; HBV DNA; anti-HBc;
D O I
10.1016/j.jhep.2005.06.016
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The infectivity of occult hepatitis B virus (HBV), defined as HBsAg-negative but HBV DNA-positive, after transfusion has been low but not negligible. To address this, we investigated the incidence of post-transfusion HBV infection after receiving screened blood units in Taiwan. Methods: Consecutive HBV-naive (anti-HBc-negative) recipients with normal ALT were followed for HBV DNA and serologic markers before and after transfusion. Among 4448 blood recipients, 467 (10.5%) were anti-HBc-negative. Post-transfusion 6-month follow-up was completed for 327. We identified 5 (1.5 %) who developed hepatitis B viremia 1 week after transfusion. Three were children who later seroconverted to anti-HBc but with normal ALT indicating subclinical acute infection, despite all had anti-HBs from previous vaccination. One had transient transfusion-transmitted HBV without seroconversion to anti-HBc and one possibly had occult HBV infection. Our findings suggested the possibility that occult HBV infection was transmissible by transfusion. The incidence of post-transfusion acute HBV infection was 0.9% (100 per million units) in naive recipients in Taiwan, a figure 7 similar to 40-fold higher than in developed countries. Moreover, some vaccinated children with anti-HBs were still susceptible. Conclusions: Therefore, despite active immunization, sensitive screening assays for occult HBV infection such as nucleic acid amplification test could be considered in endemic areas. (c) 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 46
页数:8
相关论文
共 48 条
[31]   Trends in residual risk of transfusion-transmitted viral infections (HIV, HCV, HBV) in France between 1992 and 2002 and impact of Nucleic Acid Testing [J].
Pillonel, J ;
Laperche, S .
TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2004, 11 (02) :81-86
[32]   Infectivity of blood from PCR-positive, HBsAg-negative, anti-HBs-positive cases of resolved hepatitis B infection [J].
Prince, AM ;
Lee, DH ;
Brotman, B .
TRANSFUSION, 2001, 41 (03) :329-332
[33]  
Rawal BD, 1998, TRANSFUSION, V38, p91S
[34]  
Roth WK, 2000, VOX SANG, V78, P257
[35]   Prevention of transfusion-transmitted hepatitis [J].
Sacher, RA ;
Schreiber, GB ;
Kleinman, SH .
LANCET, 2000, 355 (9201) :331-332
[36]   The risk of transfusion-transmitted viral infections [J].
Schreiber, GB ;
Busch, MP ;
Kleinman, SH ;
Korelitz, JJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (26) :1685-1690
[37]   Hepatitis C virus transmission by a blood donation negative in nucleic acid amplification tests for viral RNA [J].
Schüttler, CG ;
Caspari, G ;
Jursch, CA ;
Willems, WR ;
Gerlich, WH ;
Schaefer, S .
LANCET, 2000, 355 (9197) :41-42
[38]   SERUM HEPATITIS-B VIRUS-DNA IN HEALTHY HBSAG-NEGATIVE CHINESE ADULTS EVALUATED BY POLYMERASE CHAIN-REACTION [J].
SHIH, LN ;
SHEU, JC ;
WANG, JT ;
HUANG, GT ;
YANG, PM ;
LEE, HS ;
SUNG, JL ;
WANG, TH ;
CHEN, DS .
JOURNAL OF MEDICAL VIROLOGY, 1990, 32 (04) :257-260
[39]   NAT of the United States and Canadian blood supply [J].
Stramer, SL ;
Caglioti, S ;
Strong, DM .
TRANSFUSION, 2000, 40 (10) :1165-1168
[40]   Detection of HIV-1 and HCV infections among antibody-negative blood donors by nucleic acid-amplification testing [J].
Stramer, SL ;
Glynn, SA ;
Kleinman, SH ;
Strong, DM ;
Caglioti, S ;
Wright, DJ ;
Dodd, RY ;
Busch, MP .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (08) :760-768