Enumeration of antigen-specific CD8+ T lymphocytes by single-platform, HLA tetramer-based flow cytometry:: A European multicenter evaluation

被引:20
|
作者
Heijnen, IAFM [1 ]
Barnett, D
Arroz, MJ
Barry, SM
Bonneville, M
Brando, B
D'hautcourt, JL
Kern, F
Tötterman, TH
Marijt, EWA
Bossy, D
Preijers, FWMB
Rothe, G
Gratama, JW
机构
[1] Kantonsspital Aarau, Dept Lab Med, Div Immunol, CH-5001 Aarau, Switzerland
[2] Royal Hallamshire Hosp, Dept Hematol, Sheffield, S Yorkshire, England
[3] Hosp Egas Moniz SA, Flow Cytometry Unit, Lisbon, Portugal
[4] Royal Free Hosp, Dept Clin Immunol, London, England
[5] Inst Biol, INSERM Unite 463, Nantes, France
[6] Osped Niguarda Ca Granda, Transplant Immunol & Hematol Lab, Milan, Italy
[7] Hop Warquignies, Lab Cytometr, Boussu, Belgium
[8] Univ Hosp Charite, Inst Med Immunol, Berlin, Germany
[9] Univ Uppsala Hosp, Dept Clin Immunol, Uppsala, Sweden
[10] Leiden Univ, Med Ctr, Dept Hematol, Leiden, Netherlands
[11] Beckman Coulter, Immunom Operat, Marseille, France
[12] Radboud Univ Nijmegen Med Ctr, Cent Hematol Lab, Nijmegen, Netherlands
[13] Univ Regensburg, Inst Clin Chem & Lab Med, Regensburg, Germany
[14] Erasmus MC, Dept Internal Oncol, Lab Clin & Tumor Immunol, Rotterdam, Netherlands
关键词
tetramer; flow cytometry; CD8 T cells; multicenter evaluation; standardization;
D O I
10.1002/cyto.b.20028
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: HLA class I peptide tetramers represent powerful diagnostic tools for detection and monitoring of antigen-specific CD8(+) T cells. The impetus for the current multicenter study is the critical need to standardize tetramer flow cytometry if it is to be implemented as a routine diagnostic assay. Hence, the European Working Group on Clinical Cell Analysis set out to develop and evaluate a single-platform tetramer-based method that used cytomegalovirus (CMV) as the antigenic model. Methods: Absolute numbers of CMV-specific CD8(+) T cells were obtained by combining the percentage of tetramer-binding cells with the absolute CD8(+) T-cell count. Six send-outs of stabilized blood from healthy individuals or CMV-carrying donors with CMV-specific CD8(+) T-cell counts of 3 to 10 cells/mul were distributed to 7 to 16 clinical sites. These sites were requested to enumerate CD8(+) T cells and, in the case of CMV-positive donors, CMV-specific subsets on three separate occasions using the standard method.
引用
收藏
页码:1 / 13
页数:13
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