Analysis of FOXP3 protein expression in human CD4+CD25+ regulatory T cells at the single-cell level

被引:489
作者
Roncador, G
Brown, PJ
Maestre, L
Hue, S
Martínez-Torrecuadrada, JL
Ling, KL
Pratap, S
Toms, C
Fox, BC
Cerundolo, V
Powrie, F
Banham, AH
机构
[1] Ctr Nacl Invest Oncol, Biotechnol Program, Monoclonal Antibodies Unit, Madrid, Spain
[2] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
[3] CNIO, Biotechnol Program, Prot Technol Unit, Madrid, Spain
[4] Univ Oxford, Weatherall Inst Mol Med, Oxford, England
基金
英国医学研究理事会;
关键词
FOXP3; regulatory T cell; monoclonal antibody; lymphoma;
D O I
10.1002/eji.200526189
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The transcription factor FOXP3 plays a key role in CD4(+)CD25(+) regulatory T cell function and represents a specific marker for these cells. Despite its strong association with regulatory T cell function, in humans little is known about the frequency of CD4+CD25+ cells that express FOXP3 protein nor the distribution of these cells in vivo. Here we report the characterization of seven anti-FOXP3 monoclonal antibodies enabling the detection of endogenous human FOXP3 protein by flow cytometry and immunohistochemistry. Flow-cytometric analysis showed that FOXP3 was expressed by the majority of CD4(+)CD25(high) T cells in peripheral blood. By contrast, less than half of the CD4(+)CD25(int) population were FOXP3(+), providing an explanation for observations in human T cells that regulatory activity is enriched within the CD4(+)CD25(high) pool. Although FOXP3 expression was primarily restricted to CD4(+)CD25(+) cells, it was induced following activation of both CD4(+) and CD8(+) T cell clones. These findings indicate that the frequency of FOXP3(+) cells correlates with the level of expression of CD25 in naturally arising regulatory T cells and that FOXP3 protein is expressed by some activated CD4(+) and CD8(+) T cell clones. These reagents represent valuable research tools to further investigate FOXP3 function and are applicable for routine clinical use.
引用
收藏
页码:1681 / 1691
页数:11
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