| Literature DB >> 25636378 |
Jennifer Cuellar-Rodriguez1, Alexandra F Freeman1, Jennifer Grossman2, Helen Su3, Mark Parta4, Heardley Murdock3, Nirali Shah5, Catherine Bollard6, Heidi H Kong7, Niki Moutsopoulos8, Kelly Stone9, Juan Gea-Banacloche10, Steven M Holland1, Dennis D Hickstein11.
Abstract
We performed allogeneic hematopoietic stem cell transplantation in 6 patients with mutations in the dedicator-of-cytokinesis-8 (DOCK8) gene using a myeloablative conditioning regimen consisting of busulfan 3.2 mg/kg/day i.v. for 4 days and fludarabine 40 mg/m(2)/day for 4 days. Three patients received allografts from matched related donors and 3 patients from matched unrelated donors. Two patients received peripheral blood stem cells and 4 patients bone marrow hematopoietic stem cells. Tacrolimus and short-course methotrexate on days 1, 3, 6, and 11 were used for graft-versus-host-disease (GVHD) prophylaxis. All 6 patients are alive at a median follow-up of 22.5 months (range, 14 to 35). All patients achieved rapid and high levels of donor engraftment and complete reversal of the clinical and immunologic phenotype. Adverse events consisted of acute skin GVHD in 2 patients and post-transplant pulmonary infiltrates in a patient with extensive bronchiectasis pretransplant. Thus, a uniform myeloablative conditioning regimen followed by allogeneic hematopoietic stem cell transplantation in DOCK8 deficiency results in reconstitution of immunologic function and reversal of the clinical phenotype with a low incidence of regimen-related toxicity. Published by Elsevier Inc.Entities:
Keywords: Allogeneic; DOCK8 deficiency; Transplantation
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Year: 2015 PMID: 25636378 PMCID: PMC4426076 DOI: 10.1016/j.bbmt.2015.01.022
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742