Molero T, Roemer B, Perera Alvarez M del Mar, Lemes A, Iñigo S de la Iglesia, Palacios G, Scott C S
Servicio de Hematologia y Hemoterapia, Hospital de Gran Canaria Dr Negrín, Barranco de la Ballena, Las Palmas, Gran Canaria, Spain.
Clin Lab Haematol. 2005 Aug;27(4):224-34. doi: 10.1111/j.1365-2257.2005.00695.x.
This communication details a method for the quantitative and qualitative analysis of blood T-, B- and NK-cell populations using the Abbott Cell-Dyn CD4000 haematology analyser. A series of 66 ethylenediaminetetraacetic acid (EDTA)-anticoagulated samples with lymphocyte counts between 0.2 and 33.3 x 10(9)/l were selected and analysed with CD3, CD19, Ia and CD56 monoclonal reagents. The flow cytometry reference method utilized a lymphocyte gate defined by optical scatter, with phenotypic analyses referencing to this gate and the absolute lymphocyte count. The CD4000 method analysed all leucocyte events, set primary gates for specific immunophenotypic fractions, and then determined population counts by reference to the white blood cell (WBC) count. Comparisons of CD3+ T-cell and CD19+ B-cell numbers showed high coefficients of correlation (R(2) > 0.95) and agreement (y = 1.01x) between the CD4000 and flow cytometry reference methods. Lower coefficients of correlation were obtained for CD3-CD56+ (R(2) = 0.52) and CD3+CD56+ (R(2) = 0.83) components. No major discrepancies were observed, and the CD4000 procedures additionally provided qualitative insights into the possibility of T-cell activation. The potential to undertake immediate analysis of EDTA-anticoagulated blood samples to determine the nature of abnormal lymphocyte morphology or numbers represents a considerable advance in the capability of haematology laboratories.
本通讯详细介绍了一种使用雅培Cell-Dyn CD4000血液分析仪对血液T细胞、B细胞和NK细胞群体进行定量和定性分析的方法。选取了66份乙二胺四乙酸(EDTA)抗凝样本,淋巴细胞计数在0.2至33.3×10⁹/L之间,并用CD3、CD19、Ia和CD56单克隆试剂进行分析。流式细胞术参考方法利用光学散射定义淋巴细胞门,表型分析以此门和绝对淋巴细胞计数为参照。CD4000方法分析所有白细胞事件,为特定免疫表型组分设置初级门,然后参照白细胞(WBC)计数确定群体计数。CD3⁺T细胞和CD19⁺B细胞数量的比较显示,CD4000方法与流式细胞术参考方法之间具有高度相关性系数(R²>0.95)和一致性(y = 1.01x)。CD3⁻CD56⁺(R² = 0.52)和CD3⁺CD56⁺(R² = 0.83)组分的相关性系数较低。未观察到重大差异,并且CD4000程序还提供了关于T细胞活化可能性的定性见解。对EDTA抗凝血液样本进行即时分析以确定异常淋巴细胞形态或数量性质的潜力代表了血液学实验室能力的显著进步。