Centre de Thérapie Cellulaire et Génique, Institut Paoli-Calmettes, Marseille, France.
Cytotherapy. 2009;11(6):804-6, 806.e1. doi: 10.3109/14653240903092628.
Guidelines for flow cytometric enumeration of CD34(+) hematopoietic stem cells (HSC) recommend the use of a single-platform assay. The SCE kit has recently been commercialized by BD Biosciences. Results obtained with this newly available kit were compared with CD34(+) cell enumerations obtained in parallel with already commercialized diagnostic kits; fresh peripheral blood, apheresis, cord blood (CB) and bone marrow (BM) samples, as well as thawed apheresis and CB samples, were assayed. The SCE kit produced data for CD34(+) enumeration that correlate well with data produced with the older assays (r(2) > or = 0.9). Practical advantages were the ability to enumerate viable CD34 cells in all kinds of HSC products, the absence of bead pipetting (which decreases results precision) and a gating strategy complying with international recommendations. A major disadvantage was the absence of specific software for data analyses and presentation of results.
流式细胞术计数 CD34(+)造血干细胞(HSC)的指南建议使用单一平台检测。BD Biosciences 公司最近已将 SCE 试剂盒商业化。使用该新试剂盒获得的结果与同时使用已商业化的诊断试剂盒平行获得的 CD34(+)细胞计数进行了比较;新鲜外周血、单采、脐血(CB)和骨髓(BM)样本以及解冻的单采和 CB 样本均进行了检测。SCE 试剂盒产生的 CD34(+)计数数据与较旧的检测方法(r(2)≥0.9)产生的数据相关性良好。实际优势在于能够对各种 HSC 产品中的有活力的 CD34 细胞进行计数,无需进行珠子移液(这会降低结果的精密度),并且采用符合国际建议的门控策略。主要缺点是缺乏用于数据分析和结果表示的专用软件。