The Japanese Journal of Pediatric Hematology
Online ISSN : 1884-4723
Print ISSN : 0913-8706
ISSN-L : 0913-8706
Successful Treatment of Severe Aplastic Anemia by Allogeneic Bone Marrow Transplantation from an HbsAg-Positive Sibling with Lamivudine Administration before Bone Marrow Harvest
Koji AMANOKeita TERASHIMAMasanori NAKAMURAYoshifumi TAKASHIMAYasuo HORIKOSHIJun-ichi MIMAYA
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2002 Volume 16 Issue 6 Pages 359-362

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Abstract
An 8-year-old Japanese girl with severe aplastic anemia who did not respond to immunosuppressive therapy underwent allogeneic bone marrow transplantation (BMT) from her HBsAg-positive HLA-identical brother. To decrease his serum HBV-DNA level, lamivudine was administered to him 7 weeks before bone marrow harvest. The pretransplant conditioning regimen consisted of cyclophosphamide and anti-thymocyte globulin, and bone marrow cells (3.38 × 108 cells/kg) were then infused after plasma depletion. In order to neutralize HBV with anti-HbsAb, HB immune globulin was infused on days 0, 1 and 2. The clinical course was uneventful, and hematological recovery occurred rapidly. Her HBsAg status remained persistently negative throughout the posttransplant periods, indicating that HBV has not been transmitted to her. Lamivudine administration to the HBsAg-positive bone marrow donor may be useful to prevent HBV infection.
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