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EuroFlow standardization of flow cytometer instrument settings and immunophenotyping protocols

机译:EuroFlow流式细胞仪仪器设置和免疫表型协议标准化

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摘要

The EU-supported EuroFlow Consortium aimed at innovation and standardization of immunophenotyping for diagnosis and classification of hematological malignancies by introducing 8-color flow cytometry with fully standardized laboratory procedures and antibody panels in order to achieve maximally comparable results among different laboratories. This required the selection of optimal combinations of compatible fluorochromes and the design and evaluation of adequate standard operating procedures (SOPs) for instrument setup, fluorescence compensation and sample preparation. Additionally, we developed software tools for the evaluation of individual antibody reagents and antibody panels. Each section describes what has been evaluated experimentally versus adopted based on existing data and experience. Multicentric evaluation demonstrated high levels of reproducibility based on strict implementation of the EuroFlow SOPs and antibody panels. Overall, the 6 years of extensive collaborative experiments and the analysis of hundreds of cell samples of patients and healthy controls in the EuroFlow centers have provided for the first time laboratory protocols and software tools for fully standardized 8-color flow cytometric immunophenotyping of normal and malignant leukocytes in bone marrow and blood; this has yielded highly comparable data sets, which can be integrated in a single database.
机译:欧盟支持的EuroFlow联盟旨在通过引入8色流式细胞术,完全标准化的实验室程序和抗体检测试剂盒,对血液学恶性肿瘤的诊断和分类进行免疫表型的创新和标准化,从而在不同实验室之间获得最大的可比性结果。这需要选择兼容的荧光染料的最佳组合,并设计和评估适当的标准操作程序(SOP),以进行仪器设置,荧光补偿和样品制备。此外,我们开发了用于评估单个抗体试剂和抗体面板的软件工具。每个部分都描述了根据现有数据和经验对实验进行评估与采用的评估。基于严格执行EuroFlow SOP和抗体检测小组,多中心评估显示出高水平的可重复性。总体而言,经过6年的广泛合作实验以及对EuroFlow中心的数百例患者和健康对照的细胞样本进行分析,首次为正常和恶性肿瘤的完全标准化8色流式细胞仪免疫分型提供了实验室操作规程和软件工具骨髓和血液中的白细胞;这产生了高度可比的数据集,可以将其集成到单个数据库中。

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