Dvorak Christopher C, Horn Biljana N, Puck Jennifer M, Czechowicz Agnieszka, Shizuru Judy A, Ko Rose M, Cowan Morton J
Division of Pediatric Allergy, Immunology and Blood and Marrow Transplant, University of California San Francisco Benioff Children's Hospital, San Francisco, CA, USA.
Pediatr Transplant. 2014 Sep;18(6):602-8. doi: 10.1111/petr.12309. Epub 2014 Jun 30.
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.
对于重症联合免疫缺陷(SCID)婴儿,异基因造血干细胞移植(HCT)前的理想预处理方案应省略细胞毒性化疗,以尽量减少短期和长期并发症。我们进行了一项前瞻性试点试验,给予宿主粒细胞集落刺激因子(G-CSF)加普乐沙福,以从其龛位动员造血干细胞(HSC)。我们招募了6名接受CD34选择的单倍体相合细胞的患者和1名接受T细胞充足的匹配无关骨髓的患者。所有接受G-CSF和普乐沙福的患者,其CD34(+)细胞和Lin(-) CD34(+) CD38(-) CD90(+) CD45RA(-) HSC的动员情况总体较差,并产生了供体T细胞,但没有供体髓系或B细胞植入。尽管耐受性良好,但单独使用G-CSF加普乐沙福未能克服供体植入的物理障碍。