Co-transfusion of haplo-identical hematopoietic and mesenchymal stromal cells to treat a patient with severe aplastic

Abstract A 3-year-old girl with severe aplastic anemia (SAA) that was unresponsive to steroid, cyclosporine and filgrastim treatments received bone marrow (BM) mesenchymal stromal cells (MSC; 1.25 × 106 /kg), granulocyte colony-stimulating factor (G-CSF)-mobilized BM and peripheral blood stem cell g...

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Veröffentlicht in:Cytotherapy (Oxford, England) England), 2010-07, Vol.12 (4), p.563-565
Hauptverfasser: Wang, Hengxiang, Wang, Zhidong, Xue, Mei, Liu, Jing, Yan, Hongmin, Guo, Zikuan
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Sprache:eng
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Zusammenfassung:Abstract A 3-year-old girl with severe aplastic anemia (SAA) that was unresponsive to steroid, cyclosporine and filgrastim treatments received bone marrow (BM) mesenchymal stromal cells (MSC; 1.25 × 106 /kg), granulocyte colony-stimulating factor (G-CSF)-mobilized BM and peripheral blood stem cell grafts from her father. Prior to stem cell transplantation, she had experienced repeated bacterial infections and received 44 blood transfusions during 8 months after diagnosis. The conditioning regimen consisted of fludarabine, cyclophosphamide and busulfan, and prophylaxis of acute graft-versus-host disease (GvHD) was performed by administration of anti-CD25 monoclonal antibody, cyclosporine A, methotrexate, mycophenolate mofetil and anti-thymocyte globulin. The patient achieved rapid hematopoietic engraftment of donor origin and no acute or chronic GvHD was observed. She is now alive with a good performance status, and the dose of cyclosporine A is being tapered. The novel regimen described here might be a suitable option for children with SAA who lack immediate access to HLA-matched sources.
ISSN:1465-3249
1477-2566
DOI:10.3109/14653241003695059