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普乐沙福辅助治疗在重度联合免疫缺陷的低强度预处理异基因造血细胞移植中的试验。

A trial of plerixafor adjunctive therapy in allogeneic hematopoietic cell transplantation with minimal conditioning for severe combined immunodeficiency.

作者信息

Dvorak Christopher C, Horn Biljana N, Puck Jennifer M, Czechowicz Agnieszka, Shizuru Judy A, Ko Rose M, Cowan Morton J

机构信息

Division of Pediatric Allergy, Immunology and Blood and Marrow Transplant, University of California San Francisco Benioff Children's Hospital, San Francisco, CA, USA.

出版信息

Pediatr Transplant. 2014 Sep;18(6):602-8. doi: 10.1111/petr.12309. Epub 2014 Jun 30.

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.

摘要

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。

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