Toren A, Nagler A, Amariglio N, Neumann Y, Golan H, Bilori B, Kaplinsky C, Mandel M, Biniaminov M, Levanon M, Rosenthal E, Davidson J, Brok-Simoni F, Rechavi G
The Department of Pediatric Hemato/Oncology and BMT, and the Institute of Hematology, the Chaim Sheba Medical Center, Tel-Hashomer, Israel.
Bone Marrow Transplant. 1999 Feb;23(4):405-8. doi: 10.1038/sj.bmt.1701578.
A 2-month-old girl with severe combined immunodeficiency (SCID), presented with mild staphylococcal skin infection, lymphopenia, low T cell number, absence of B cells, high number of NK cells, and a negligible response to mitogens. Since her older brother died as a result of SCID 2 years earlier, cord blood was harvested from a sister born 2 1/2 years earlier, who was normal and fully matched both by serology and molecular typing. In view of her clinical condition and in spite of a high number of NK cells with normal activity, HUCBT without preparative conditioning was performed. No G-CSF was administered. Engraftment with mixed chimerism was evident 3 weeks post transplantation. There were no peritransplantation complications. Eighteen months post transplantation, the girl is in excellent condition, blood counts are normal, T cell engraftment is complete, B cell engraftment is proceeding gradually, and the mitogen stimulation tests are normal. Due to the unique nature of HUCB hematopoietic cells, engraftment without conditioning may be possible in patients with SCID with fully matched donors. This is the first HUCBT performed without conditioning.
一名患有严重联合免疫缺陷(SCID)的2个月大女孩,出现轻度葡萄球菌皮肤感染、淋巴细胞减少、T细胞数量低、B细胞缺失、NK细胞数量高以及对丝裂原反应可忽略不计。由于她的哥哥2年前因SCID死亡,从2年半前出生的一个姐姐那里采集了脐血,该姐姐正常,血清学和分子分型均完全匹配。鉴于她的临床状况,尽管NK细胞数量多且活性正常,但未进行预处理就进行了脐血造血干细胞移植(HUCBT)。未给予粒细胞集落刺激因子(G-CSF)。移植后3周明显出现混合嵌合体植入。没有移植相关并发症。移植后18个月,女孩状况良好,血细胞计数正常,T细胞植入完全,B细胞植入正在逐渐进行,丝裂原刺激试验正常。由于脐血造血细胞的独特性质,对于有完全匹配供体的SCID患者,不进行预处理也可能实现植入。这是首次未进行预处理的脐血造血干细胞移植。