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阿仑单抗辅助治疗用于严重联合免疫缺陷的低强度预处理异基因造血细胞移植的试验。

A trial of alemtuzumab 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, Adams Stuart, Veys Paul, Czechowicz Agnieszka, 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):609-16. doi: 10.1111/petr.12310. 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 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.

摘要

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。

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Radiosensitive severe combined immunodeficiency disease.辐射敏感型严重联合免疫缺陷病。
Immunol Allergy Clin North Am. 2010 Feb;30(1):125-42. doi: 10.1016/j.iac.2009.10.004.

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