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作 者:魏征[1] 王志梅[1] 庄静丽[1] 李锋[1] 程韵枫[1] 邹善华[1]
机构地区:[1]复旦大学附属中山医院血液科,上海200032
出 处:《白血病.淋巴瘤》2013年第5期286-290,共5页Journal of Leukemia & Lymphoma
摘 要:目的通过血细胞分析仪检测外周血造血祖细胞(HPC)含量,探寻一种快速预测采集物干细胞含量、判断外周血造血干细胞采集时机的手段,并评价其应用意义。方法对27例化疗联合粒细胞集落刺激因子(G.CSF)进行外周血造血干细胞动员采集者及17例单用G—CSF动员的采集者,利用血细胞分析仪检测外周血HPC计数,血液治疗和移植工程国际组织(ISHAGE)法检测外周血及采集物CD;细胞计数,并进行相关回归分析。对外周血HPC计数预测采集物CD;含量进行受试者工作曲线(ROC)分析。结果无论化疗组或非化疗组,外周血HPC计数与CD;计数均具有线性相关性(r=0.711,P=0.000及r=0.656,P=0.004)。化疗组外周血CD;计数=-0.829+0.648×外周血HPC计数;非化疗组外周血CD;细胞计数=45.033+0.460×外周血HPC计数。化疗组患者外周血HPC计数与采集物CD;细胞量呈线性相关(r=0.602,P=0.001),采集物CD;计数=1.106+0.046×外周血HPC计数。以HPC≥85/μl预测采集物CD;计数≥5×106/kg的灵敏度为78%,特异度为82%。结论在自体干细胞移植动员患者中,外周血HPC计数可部分替代外周血CD5计数预测采集效果,HPC≥85/μl为较好的预测阈值。Objective To evaluate a method of fast detection of the hematopoietic progenitor cell (HPC) in peripheral blood samples and explore for an appropriate cutoff value in prediction of adequate CD3+4 cell in apheresis concentrate. Methods Peripheral blood samples and apheresis concentrate samples were collected from 27 auto-PBSCT patients receiving chemotherapy plus G-CSF mobilization (chemo group) and 17 patients receiving G-CSF alone (non-chemo group). CD;4 cell counts were determined by flow cytometry according to ISHAGE guideline and HPC counts were detected using Sysmex XE-2100 automatic hemocyte analyzer. The correlation between HPC and CD ;4 cell counts in peripheral blood samples and apheresis concentrates were analyzed. Receiver operating characteristic (ROC) curves was used to determine the cutoff value in prediction of adequate CD3+4 cell in apheresis concentrate. Results CD3+4 cell counts in peripheral blood samples can be estimated by HPC counts (r = 0.711, P = 0.000, r = 0.656, P = 0.004). CD3+4 cell counts = -0.829+0.648xHPC counts (in chemo group) or 45.033+0.460×HPC counts (in non-chemo group). HPC counts in the peripheral blood of auto-PBSCT patients were highly correlated with the CD34 cell yield (r = 0.602, P = 0.001), CD3+4 cell counts = 1.106+0.046×HPC counts. When HPC in peripheral blood was 85/1.d, the prediction of adequate CD3+4 cells in the yield of apheresis (≥5×106/kg body weight) would have a sensitivity of 78 % and a specifity of 82 %. Conclusion HPC counts in peripheral blood samples in auto-PBSCT patients can be used to determine the optimal time of apheresis and be used as a good marker to predict the stem cell in the yield.
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