Dvorak Christopher C, Horn Biljana N, Puck Jennifer M, Adams Stuart, Veys Paul, Czechowicz Agnieszka, 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):609-16. doi: 10.1111/petr.12310. 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 alemtuzumab monotherapy to overcome NK-cell mediated immunologic barriers to engraftment. We enrolled four patients who received CD34-selected haploidentical cells, two of whom failed to engraft donor T cells. The two patients who engrafted had delayed T-cell reconstitution, despite rapid clearance of circulating alemtuzumab. Although well-tolerated, alemtuzumab failed to overcome immunologic barriers to donor engraftment. Furthermore, alemtuzumab may slow T-cell development in patients with SCID in the setting of a T-cell depleted graft.
对于重症联合免疫缺陷(SCID)婴儿,在异基因造血干细胞移植(HCT)前,理想的预处理方案应避免使用细胞毒性化疗,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,采用阿仑单抗单药治疗,以克服自然杀伤(NK)细胞介导的植入免疫障碍。我们招募了4例接受CD34选择的单倍体相合细胞的患者,其中2例未能植入供体T细胞。尽管循环中的阿仑单抗迅速清除,但成功植入的2例患者T细胞重建延迟。尽管耐受性良好,但阿仑单抗未能克服供体植入的免疫障碍。此外,在T细胞耗竭的移植物情况下,阿仑单抗可能会减缓SCID患者的T细胞发育。