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高表达CD123的CD34+CD19+细胞为Ph染色体阳性急性淋巴细胞白血病复发预测的新标记 被引量:1

CD34^+ CD19^+ Cells with CD123 Overexpression Are A Novel Prognostic Marker in Ph Chromosome-positive Acute Lymphoblastic Leukemia
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摘要 本研究探讨CD123在成人Ph染色体阳性急性淋巴细胞白血病(Ph chromosome-positive acute lymphoblastic leukemia,Ph+ALL)患者CD34+CD19+细胞上的表达特点及其在复发预测中的作用。2010年1月-2012年4月北京大学血液病研究所经规范化诊治的49例18-60岁初诊Ph+ALL患者纳入本研究,在初诊及治疗后不同时间点通过多色流式细胞术监测CD34+CD19+细胞上CD123的荧光强度及表达比例,同时利用实时定量聚合酶链式反应(real-time quantitative polymerase chain reaction,RQ-PCR)监测BCR-ABL1融合基因变化。与正常B祖细胞相比,获得完全缓解后任意时间点骨髓标本中异常高表达CD123的CD34+CD19+细胞大于10个定义为免疫残留阳性(FCM阳性)。结果表明,①初诊及复发Ph+ALL患者CD34+CD19+细胞上CD123的平均荧光强度(mean fluoresce intensity,MFI)〔8.52(3.71-32.35)vs 8.93(4.79-29.74)vs 1.31(0.21-1.75),P<0.05〕,以及异常高表达CD123的CD34+CD19+细胞比例〔84.63%(55.07%-99.96%)vs 84.50%(57.68%-99.80%)vs 0.99%(0.45%-1.83%),P<0.05〕均显著高于健康供者的正常B祖细胞。入组的全部初诊及复发Ph+ALL患者的CD34+CD19+细胞均高表达CD123。②多色流式细胞术监测异常高表达CD123的CD34+CD19+细胞和RQ-PCR检测BCR-ABL1融合基因的结果之间具有良好的相关性(n=49例,360对,Spearman r=0.90,P<0.0001)。③13例复发患者中有11例在复发前3个月MRD监测表明,在复发前中位时间60(30-73)天均检出FCM阳性。结论:通过多色流式细胞术检测异常高表达CD123的CD34+CD19+细胞可与RQ-PCR检测BCR-ABL1融合基因互为补充,共同应用于Ph+ALL患者的MRD监测以及复发预测。 This study was aimed to investigate the characteristics of CD123 expression on CD34 + CDl9 + cells and its prognostic significance as a novel MRD biomarker in Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) patients.Consecutive newly diagnosed Ph + ALL patients (n =49) in Peking University Institute of Hematology from January 2010 to April 2012 were prospectively enrolled in this study.At diagnosis and different time points during treatment,CD123 expression on CD34 + CD19 + cells was examined by multiparameter flow cytometry (MFC).More than 10 CD34 + CD19 + cells with CDl23 overexpression in bone marrow samples after complete remission were defined as FCM positive (FCM +).The BCR-ABL1 transcript was detected by real-time quantitative polymerase chain reaction (RQ-PCR) concurrently.The results showed that mean fluorescence intensity of CD123 on CD34+ CD19 + cells in newly diagnosed Ph + ALL and relapsed Ph + ALL patients was significantly higher than that of normal B-cell progenitors [8.52 (3.71-32.35) vs 8.93 (4.79-29.74) vs 1.31 (0.21-1.75),P < 0.05].In addition,ratio of the CD34 +CD19 + cells with CD123 overexpression in newly diagnosed Ph + ALL and relapsed Ph+ ALL patients were significantly higher than that of normal B-cell progenitors [84.63% (55.07%-99.96%) vs 84.50% (57.68%-99.80%) vs 0.99% (0.45 %-1.83 %),P < 0.05].CD34 + CD19 + cells with CD123 overexpression were detected in all newly diagnosed and relapsed Ph + ALL patients.A good correlation was found between the MRD results of CD34 + CD19 + cells with CD123 overexpression detected by MFC and that detected by RQ-PCR (n =360 pairs,Spearman r =0.90,P <0.0001).Among 13 cases relapsed during follow up,11 cases of them were detected by FCM+ at a median time of 60 (30-73) days before the recurrence.It is concluded that as a complementary to RQ-PCR,detection of the CD34 +CD19 + cells with CD123 overexpression by MFC promises to be an efficient tool for MRD assessment and risk stratification in human Ph + ALL.
出处 《中国实验血液学杂志》 CAS CSCD 北大核心 2014年第1期6-10,共5页 Journal of Experimental Hematology
基金 国家重大科学仪器设备开发专项(2011YQ03013407) 国家自然科学基金项目(81370638) 北京市科技计划项目(Z111107067311070)
关键词 CD123 CD34+ CD19+细胞 急性淋巴细胞白血病 PH染色体 CD123 CD34 + CD19 + cell acute lymphoblastic leukemia Ph chromosome
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