| Literature DB >> 24977650 |
Christopher C Dvorak1, Biljana N Horn, Jennifer M Puck, Agnieszka Czechowicz, Judy A Shizuru, Rose M Ko, Morton J Cowan.
Abstract
For infants with SCID, the ideal conditioning regimen before allogeneic HCT would omit cytotoxic chemotherapy to minimize short- and long-term complications. We performed a prospective pilot trial with G-CSF plus plerixafor given to the host to mobilize HSC from their niches. We enrolled six patients who received CD34-selected haploidentical cells and one who received T-replete matched unrelated BM. All patients receiving G-CSF and plerixafor had generally poor CD34(+) cell and Lin(-) CD34(+) CD38(-) CD90(+) CD45RA(-) HSC mobilization, and developed donor T cells, but no donor myeloid or B-cell engraftment. Although well tolerated, G-CSF plus plerixafor alone failed to overcome physical barriers to donor engraftment.Entities:
Keywords: engraftment; haploidentical; plerixafor; severe combined immunodeficiency
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Year: 2014 PMID: 24977650 PMCID: PMC5413354 DOI: 10.1111/petr.12309
Source DB: PubMed Journal: Pediatr Transplant ISSN: 1397-3142