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作 者:唐暐[1] 王苓[1] 赵维莅[1] 沈志祥[1] 胡炯[1]
机构地区:[1]上海交通大学医学院附属瑞金医院血液科,200025
出 处:《白血病.淋巴瘤》2010年第5期265-268,共4页Journal of Leukemia & Lymphoma
摘 要:目的 研究外周血CD34^+细胞数对采集结果 的意义,并探索可用于临床指导外周干细胞采集时机选择的参考阈值.方法 2007年1月至2009年12月共57例次自体造血干细胞移植动员采集患者,以环磷酰胺(CTX)化疗+粒细胞集落刺激因子(G-CSF)(5~10μg/kg)动员,COBE分离仪(Spectra Version 6)行外周血造血干细胞采集,应用流式细胞术监测外周血中CD34^+细胞绝对计数.结果 采集产品单个核细胞(MNC)中位数4.6×10^8/kg(0.3×10^8/kg~10.5×10^8/kg),CD34^+细胞中位数2.4×10^6/kg(0.16 × 10^6/kg~34.9×10^6/kg),外周血CD34^+细胞数是产品MNC和CD34^+细胞总量唯一相关指标,外周血白细胞(WBC)与采集产品MNC和CD34^+细胞数无关.进一步分析提示外周血CD34^+计数≥15/μl,单次采集效率提高,CD34^+细胞采集量达1×10^6/kg和2×10^6/kg比例为81%和60%,采集产品MNC和CD34^+总数明显提高.提示外周血CD34^+细胞数15/μl可作为启动采集.ROC分析发现外周血CD34^+细胞25(26.5~28.6)/μl,单次采集足量CD34^+细胞概率最大.结论 外周血CD34^+细胞计数是外周血自体干细胞采集重要的相关指标,CD34^+细胞15/μl可作为采集时机选择的阈值.Objective Autologous hematopoietic stem cell transplantation (Auto-HSCT) has been widely used in hematological malignancies.To mobilize and harvest sufficient number of peripheral CD34^+ cells is one of key issues for auto-HSCT. Peripheral CD34^+ cell numeration has been used as an indicator for apheresis while we mostly rely on the peripheral WBC or MNC count. In this study, we try to evaluate the association of peripheral CD34^+ count to the CD34^+ cells number in the apheresis product and to find out a potential threshold. Methods From Jan 2007 to Dec 2009, a total of 57 apherosis for auto-HSCT were analysed. All patients were mobilized by cyclophophamide (CTX) plus G-CSF(5-10μg/kg) regimen. The apheresis were performed with COBE SPECTRA VERSION 6 and CD34^+ count of both peripheral and apheresis products were analysed by flow cytometry. Results The median number of MNC in apheresis products was 4.6(0.3-10.5)×10^8kg with median CD34^+ cells at 2.4(0.16-34.9)×10^6kg. The peripheral CD34^+ count was the only parameter associated with the MNC and CD34^+ cell numbers in the apheresis products while the WBC number was irrelevant to the results of apheresis. Our data showed that when the peripheral CD34^+ count reach 15/μl, the efficacy of a single apheresis significantly improved with 81 % and 60 % reached 1 and 2×10^6CD34^+ cells/kg respectively and the total number of MNC and CD34^+ cells were significantly superior to apheresis with peripheral CD34^+ cells 〈15/μl, thus indicated that CD34^+ ≥15 /μl can be used as the threshold for apheresis. Furthermore, the ROC analysis demonstrated that CD34^+ cells ≥25(26.5-28.6) /μl is the best indicator level for a successful single apheresis. Conclusion Our study clearly showed that peripheral CD34^+ cell count is a key indicator of apherosis. CD34^+ cells at 15/μl can be used as the threshold to start apheresis in the clinical setting.
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