2007
DOI: 10.1038/sj.bmt.1705890
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Hematopoietic stem cell transplantation for primary immunodeficiency disease

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Cited by 66 publications
(54 citation statements)
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“…For nonprimary immunodeficiency patients, at the 12-week evaluation, if the absolute CD4 count was less than 100 cells/mm 3 and there was no evidence of active GVHD, a prophylactic infusion of 3 Â 10 4 cryopreserved donor CD3 þ cells/kg was performed. For primary immunodeficiency patients, DLI could be administered as early as 4 weeks post-HSCT if there were no detectible CD4 þ cells.…”
Section: Donor Pbsc Collection and Manipulationmentioning
confidence: 99%
See 1 more Smart Citation
“…For nonprimary immunodeficiency patients, at the 12-week evaluation, if the absolute CD4 count was less than 100 cells/mm 3 and there was no evidence of active GVHD, a prophylactic infusion of 3 Â 10 4 cryopreserved donor CD3 þ cells/kg was performed. For primary immunodeficiency patients, DLI could be administered as early as 4 weeks post-HSCT if there were no detectible CD4 þ cells.…”
Section: Donor Pbsc Collection and Manipulationmentioning
confidence: 99%
“…3 Haplocompatible donors share a single HLA haplotype with the transplant recipient. Due to the HLA disparities involved, most haplocompatible HSCT protocols utilize ex vivo T-cell depletion to avoid severe GVHD.…”
Section: Introductionmentioning
confidence: 99%
“…Selection of a suitable donor by HLA matching and/or an appropriate conditioning regimen has improved the outcome of HCT for leukemia patients 1 and PID patients. 2,3 Recently, successful outcomes of cord blood transplantation (CBT) and BM transplantation (BMT) have been observed even in HLAmismatched conditions. [4][5][6][7][8] Despite these improved outcomes, transplantation-related morbidities such as graft failure, GVHD and infection are still major problems that affect the prognosis and/or quality of life.…”
Section: Introductionmentioning
confidence: 99%
“…2,4 The optimal approach to hematopoietic SCT in children with PID who lack a matched sibling donor is controversial. 5 Some centers continue to use myeloablative conditioning regimen in children with PID who undergo HLA-mismatched related T-cell-depleted BMT associated with high risk of graft failure. 2,5 However, recent success with reduced-intensity conditioning regimen before unrelated BMT shows that this may provide better engraftment, immune reconstitution and survival for patients with PID than the previous alternative.…”
mentioning
confidence: 99%
“…5 Some centers continue to use myeloablative conditioning regimen in children with PID who undergo HLA-mismatched related T-cell-depleted BMT associated with high risk of graft failure. 2,5 However, recent success with reduced-intensity conditioning regimen before unrelated BMT shows that this may provide better engraftment, immune reconstitution and survival for patients with PID than the previous alternative. 6,7 Very few patients with this pediatric emergency have undergone transplantation choosing umbilical cord blood as a first choice of hematopoietic stem cell source, despite the significantly faster availability of banked cryopreserved umbilical cord blood units and the higher frequency of rare haplotypes compared with BM registries.…”
mentioning
confidence: 99%