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作 者:袁海龙[1] 李玲[1] 曲建华[1] 温丙昭[1] 江明[1] 郝建萍[1] 陈瑢[1] 郭新红[1] 哈力达·亚森[1] 王善征[1] 丁凌录[1]
机构地区:[1]新疆医科大学第一附属医院血液科、新疆血液病研究所,乌鲁木齐830054
出 处:《中华血液学杂志》2009年第2期82-86,共5页Chinese Journal of Hematology
基 金:基金项目:新疆维吾尔自治区高技术研究与发展计划(200511109)
摘 要:目的探讨亲属间HLA单倍体相合外周血干细胞移植(PBSCT)治疗恶性血液病的疗效。方法恶性血液病患者36例,中位年龄25(11~48)岁,供受者人类白细胞抗原(HLA)配型1个位点不合者7例,2~3个位点不合者29例。移植方案采用清髓性预处理及联合免疫抑制剂预防移植物抗宿主病(GVHD)进行非体外去T细胞的PBSCT,移植的CD34^+细胞中位数为11(4.16~21.00)×10^6/kg。结果36例患者均获得完全、持久供者造血干细胞植入,发生急性GVHD(aGVHD)15例(41.7%),均为Ⅰ-Ⅱ度;存随访时间超过18个月的29例患者中发生慢性GVHD(cGVHD)17例(58.6%)。移植后T、B、NK细胞亚群下降及恢复与HLA位点全相合移植患者差异无统计学意义。36例患者中位随访时间为15(4~69)个月,复发5例,累计复发率为13.9%。现无自血病存活30例,2年预期总无白血病生存率(LFS)为82.2%。结论应用清髓性预处理联合多种免疫抑制剂进行非体外去T细胞亲属间HLA单倍体相合PBSCT是治疗恶性血液病安全有效的方案。Objective To analyze the clinical outcome of human leukocyte antigen (HLA) hapoidentical peripheral blood stem cell transplantation (PBSCT) from related donors for hematological malignancies. Methods Thirty-six patients with hematological malignancies, with a median age of 25 ( 11 - 48 ) years, were transplanted with PBSC from an HLA-haploidentical family donors: 7 were 1 locus mismatched and 29 were 2 -3 loci mismatched. The recipients received myeloablative conditioning regimen, in combination with different immunosuppressants according to the degree of HLA disparity followed by non-T-cell depleted PBSCT. The median number of CD34^+ cells were 11 (4.16 - 21.00) × 10^6/kg. Results All patients achieved sustained,full donor-type engraftment. Fifteen patients(41.7% ) developed grade Ⅰ - Ⅱ aGVHD. Among 29 patients followed up more than 18 months,17 (58.6%) developed cGVHD. There was no statistical difference in decrease and recovery of T, B and NK cell subsets after transplantation between HLA haploidentical group and HLA identical PBSCT group. The median follow-up duration was 15 (4 -69) momths. Five patients ( 13.9% ) relapsed. The 2-year probability of leukemia-free survival (LFS) was 82.2%. Conclusion Non-T-cell depleted HLA-haploidentical PBSCT is safe and feasible for patients with hematological malignancies after myeloablative conditioning regimen combined with intensive immunosuppressants.
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