Zeidan Magda A, Kamal Howyda M, El Shabrawy Deena A, Esh Asmaa M H, Sattar Reeham H Abdel-
Clinical Pathology Department, Faculty of Medicine, Benha, Egypt.
Clinical Pathology Department, Faculty of Medicine, Benha, Egypt.
Blood Cells Mol Dis. 2016 Jul;59:113-8. doi: 10.1016/j.bcmd.2016.05.005. Epub 2016 May 9.
MRD is seen as the major cause of disease relapse. So, it gives important feedback about conventional treatment success and helps in selecting therapeutic alternatives. We aimed to compare the expression of CD34/CD123 on normal B-cell precursors in bone marrow ("hematogones") and on leukemic blasts in B-acute lymphoblastic leukemias (B-ALL) pediatric cases by flowcytometric analysis. Our study conducted on 20 children as a control and 30 B-ALL children cases at diagnosis and after 28days of induction therapy. We found that the less mature hematogones (dim CD45+) that express CD34 lack CD123 expression, whereas the more mature hematogones (moderate CD45+) lack CD34 but always express CD123. In contrast with this discordant pattern of CD34 and CD123 expression in hematogones, blasts in 24 of 30 cases (80%) of B-ALL showed concordant expression pattern of the 2 antigens: 63% (19 of 30) cases expressed both antigens, whereas 17% (5 of 30) expressed neither. Our study concluded that these distinct patterns of CD34/CD123 expression on hematogones (discordant) and B-ALL blasts (concordant) are useful in differentiating small populations of residual blasts from hematogones after induction therapy to detect MRD.
微小残留病(MRD)被视为疾病复发的主要原因。因此,它能为传统治疗的成功提供重要反馈,并有助于选择治疗方案。我们旨在通过流式细胞术分析,比较骨髓中正常B细胞前体(“造血细胞”)和B急性淋巴细胞白血病(B-ALL)儿科病例中白血病原始细胞上CD34/CD123的表达。我们对20名儿童作为对照以及30例B-ALL儿童病例在诊断时和诱导治疗28天后进行了研究。我们发现,表达CD34的较不成熟造血细胞(CD45弱阳性)缺乏CD123表达,而较成熟的造血细胞(CD45中等阳性)缺乏CD34但总是表达CD123。与造血细胞中CD34和CD123表达的这种不一致模式相反,30例B-ALL病例中有24例(80%)的原始细胞显示这两种抗原的一致表达模式:63%(30例中的19例)病例表达两种抗原,而17%(30例中的5例)既不表达。我们的研究得出结论,造血细胞(不一致)和B-ALL原始细胞(一致)上CD34/CD123表达的这些不同模式,有助于在诱导治疗后区分少量残留原始细胞与造血细胞以检测MRD。