Semi-automated and standardized cytometric procedures for multi-panel and multi-parametric whole blood immunophenotyping

被引:35
作者
Hasan, Milena [1 ]
Beitz, Benoit [1 ]
Rouilly, Vincent [1 ,2 ]
Libri, Valentina [1 ]
Urrutia, Alejandra [1 ,3 ,4 ]
Duffy, Darragh [1 ,3 ,4 ]
Cassard, Lydie [1 ]
Di Santo, James P. [5 ]
Mottez, Estelle [1 ]
Quintana-Murci, Lluis [6 ,7 ]
Albert, Matthew L. [1 ,3 ,4 ,8 ]
Rogge, Lars [1 ,9 ]
机构
[1] Inst Pasteur, Ctr Human Immunol, F-75724 Paris 15, France
[2] Inst Pasteur, Ctr Bioinformat, F-75724 Paris 15, France
[3] INSERM, U818, F-75654 Paris 13, France
[4] Inst Pasteur, Dept Immunol, Lab Dendrit Cell Immunobiol, F-75724 Paris 15, France
[5] Inst Pasteur, Dept Immunol, Lab Innate Immun, F-75724 Paris 15, France
[6] Inst Pasteur, Dept Genomes & Genet, Lab Human Evolutionary Genet, F-75724 Paris 15, France
[7] CNRS, URA3012, F-75700 Paris, France
[8] INSERM, UMS20, F-75654 Paris 13, France
[9] Inst Pasteur, Dept Immunol, Immunoregulat Lab, F-75724 Paris 15, France
关键词
Immunophenotyping; Cytometry; Whole blood; Automation; Standardization; CYTOKINE FLOW-CYTOMETRY; T-CELL SUBSETS; INFORMATION; LYMPHOCYTES; SEPARATION; MEMORY;
D O I
10.1016/j.clim.2014.12.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunophenotyping by multi-parametric flow cytometry is the cornerstone technology for enumeration and characterization of immune cell populations in health and disease. Standardized procedures are essential to allow for inter-individual comparisons in the context of population based or clinical studies. Herein we report the approach taken by the Milieu Interieur Consortium, highlighting the standardized and automated procedures used for immunophenotyping of human whole blood samples. We optimized eight-color antibody panels and procedures for staining and lysis of whole blood samples, and implemented pre-analytic steps with a semi-automated workflow using a robotic system. We report on four panels that were designed to enumerate and phenotype major immune cell populations (PMN, T, B, NK cells, monocytes and DC). This work establishes a foundation for defining reference values in healthy donors. Our approach provides robust protocols for affordable, semi-automated eight-color cytometric immunophenotyping that can be used in population-based studies and clinical trial settings. (C) 2015 The Authors. Published by Elsevier Inc.
引用
收藏
页码:261 / 276
页数:16
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