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June 2003 • Volume 37 • Number 6
Original Articles: Viral Hepatitis
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| Abstract | TOP |
The shortage of donor organs occasionally mandates the use of hepatic
allografts from anti-HBc (+) donors. HBIG and/or lamivudine are recommended for
the prevention of de novo HBV infection in naive patients, but there are
attendant problems, such as mutant strain emergence and high cost. Active
immunization presents a better alternative than the use of HBIG or lamivudine,
if it can be proven to be effective. Accordingly, we investigated the outcome of
HBV vaccination in pediatric hepatic transplant recipients. Between July 1999
and October 2001, 19 pediatric recipients were administered HBV vaccinations
after liver transplantation at Seoul National University Hospital. Nine patients
received a graft from anti-HBc (+) donors and 10 from anti-HBc (–) donors. When
steroid was withdrawn, recombinant HBV vaccine was administered. The median
follow-up period after vaccination was 10.0 ± 5.2 months. Seventeen of the 19
patients showed a positive response to vaccination. In 9 patients who received
grafts from anti-HBc (+) donors, 2 patients showed no response, 4 patients low
response (peak HBsAb titer <1,000 IU/L), and 3 patients high response (peak
HBsAb titer
1,000 IU/L).
De novo HBV infection developed in 1 of 2 patients who showed no response to
vaccination. In 10 patients who received grafts from anti-HBc (–) donors, 5
showed a low response and 5 a high response. In conclusion, HBV vaccination in
pediatric patients after liver transplantation appeared to exhibit some
effectiveness at protecting young children that received a graft from anti-HBc
(+) donors from de novo HBV infection. (HEPATOLOGY
2003;37:1329-1334.)
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| Publishing and Reprint Information | TOP |
| Copyright © 2003 by the American Association for the Study of Liver Diseases. All rights reserved. |


Hepatology is published
for the American Association for the
Study of Liver Diseases by
W.B. Saunders Company
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