成人急性髓性白血病患者白血病干细胞中CD96和CD123的流式细胞术表达及其作为预后指标的价值

IF 0.1 Q4 HEMATOLOGY
R. Ibrahim, H. Hegab, M. Elmonem, Alia M. Saeed
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引用次数: 0

摘要

背景急性粒细胞白血病(AML)是一种与复发或一线药物耐药性相关的疾病。这可归因于静止期白血病干细胞(LSC)。我们旨在确定成人AML患者LSC表面CD96和CD123的表达状态及其与预后的关系。患者和方法2017年6月至2018年2月,共有40名新发AML成年患者和40名年龄匹配和性别匹配的对照组从X中心、Y城市、Y国家招募,并进行1年随访。使用CD34、CD38、CD96和CD123单克隆抗体收集骨髓样本用于流式细胞术分析。对于病例,在诊断时和化疗后第28天采集样本,而对于对照组,采集一次样本。结果AML患者CD96和CD123的表达明显高于对照组。CD96的表达与较高的初始骨髓和外周血母细胞百分比有关。第28天CD96的表达与第0天的表达和诊断时CD123的表达呈正相关,P值分别小于0.001和0.034。与低分化亚型相比,这两种标志物在分化型AML的LSCs上的表达频率高得多(P<0.05)。这两种标记物都与较差的治疗结果有关,CD96阳性和CD123阳性病例在第28天的无进展生存率较低(分别为P=0.035和0.041)。结论CD96和CD123是未来AML治疗药物开发的潜在靶向标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of flow cytometric expressions of CD96 and CD123 on leukemic stem cells in patients with adult acute myeloid leukemia and their utility as prognostic markers
Background Acute myeloid leukemia (AML) is a disease associated with a risk of relapse or refractoriness to the frontline agents. This is attributable to the quiescent leukemic stem cells (LSC). We aimed to determine the expression status of CD96 and CD123 on the surface of LSC in adult patients with AML and their relationship to prognosis. Patients and methods A total of 40 adult patients with de novo AML and 40 age-matched and sex-matched controls were recruited from Center ‘X,’ City ‘Y,’ Country ‘Y’ from June 2017 to February 2018, with 1-year follow-up. Bone marrow samples were collected for flow cytometric analysis using CD34, CD38, CD96, and CD123 monoclonal antibodies. For cases, samples were obtained at diagnosis and on day 28 after chemotherapy, whereas for controls, samples were taken once. Results CD96 and CD123 expressions are significantly higher in patients with AML as compared with controls. CD96 expression is associated with higher initial bone marrow and peripheral blood blast percentages. Day28 CD96 expression is positively correlated with its expression on day 0 and with CD123 expression at diagnosis, with P values of less than 0.001 and 0.034, respectively. Both markers were much more frequently expressed on LSCs in differentiated AML as compared with ill-differentiated subtypes (P<0.05). Both markers are linked to poor therapy outcome, with inferior progression-free survival among CD96-positive and CD123-positive cases at day 28 (P=0.035 and 0.041, respectively). Conclusions CD96 and CD123 represent potential targetable markers for the future development of therapeutic armamentarium for AML.
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