Abstract
A sibling cord blood (CB) transplantation was performed in a boy with Wiskott–Aldrich syndrome. The CB (31 × 106 CD34+ cells) derived from a newborn sister with neonatal alloimmune thrombocytopenia (NAIT) with 40000 platelets/μl, caused by a maternal anti-HPA-5b and HLA-A2 antibody. Maternal serum did not inhibit clonogenicity after in vitro testing of megakaryopoiesis. Accordingly, this CB was accepted for sibling transplantation. The transplantation showed a good course with fast and sustained hematopoietic reconstitution (granulocytes >500/μl on day +16, platelets >50 000/μl on day +30). This case demonstrates a successful CB transplantation from a donor suffering from NAIT. Bone Marrow Transplantation (2001) 28, 803–806.
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We thank Marion Behr, Anja Pohlmeyer and Astrid Kraemer for excellent technical assistance.
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Cassens, U., Garritsen, H., Kelsch, R. et al. Platelet glycoprotein complex Ia/IIa antibodies cause neonatal alloimmune thrombocytopenia but do not inhibit megakaryopoiesis and platelet recovery after allogeneic cord blood stem cell transplantation. Bone Marrow Transplant 28, 803–806 (2001). https://doi.org/10.1038/sj.bmt.1703235
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DOI: https://doi.org/10.1038/sj.bmt.1703235