Abstract
Allogeneic BMT for severe aplastic anemia is associated with a significant rate of graft rejection, especially in patients who have been previously transfused. We report a child with aplastic anemia who rejected donor marrow twice despite adequate immunosuppression as part of the conditioning therapy but engrafted successfully following combined administration of three modalities of immunosuppression: antithymocyte globulin, total lymphoid irradiation and the monoclonal antibody Cannpath-1G. Restriction fragment length polymorphism studies > 1 year after BMT show full donor hematopoiesis with no evidence of autologous recovery.
Original language | English (US) |
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Pages (from-to) | 97-99 |
Number of pages | 3 |
Journal | Bone Marrow Transplantation |
Volume | 13 |
Issue number | 1 |
State | Published - Feb 23 1994 |
ASJC Scopus subject areas
- Hematology
- Transplantation