Abstract
We report on a boy with β-thalassemia major who developed early graft failure after double-unit unrelated cord blood transplantation, who subsequently received a myeloablative preconditioning regimen using non-T-cell-depleted PBSCT from his HLA-haploidentical 2-loci-mismatched mother. Neutrophil recovery with full donor chimerism was observed at post-transplantation day +11. Furthermore, GVHD was easy to control. The patient was transfusion-independent with complete donor chimerism eight months post-transplant. The result indicated that fetomaternal microchimerism may be an important attribute of a successful transplant. We suggested that a third allo-HSCT may be taken into consideration for patients with transfusion-dependent thalassemia who experience graft failure, even after two previous transplants.
Original language | English |
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Pages (from-to) | 232-234 |
Number of pages | 3 |
Journal | Pediatric Transplantation |
Volume | 12 |
Issue number | 2 |
DOIs | |
State | Published - 03 2008 |
Keywords
- Haploidentical 2-loci-mismatched mother
- Retransplant
- β-thalassemia major