New tools to identify regulatory T cells

被引:17
作者
Graca, L
机构
[1] Univ Lisbon, Fac Med, Inst Mol Med, Cellular Immunol Unit, P-1649028 Lisbon, Portugal
[2] Inst Gulbenkian Ciencias, Oeiras, Portugal
关键词
regulatory T cells; Foxp3; tolerance; monoclonal antibodies;
D O I
10.1002/eji.200526303
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The lack of tools for direct identification of regulatory T cells (T-reg cells) at the single-cell level has been one of the major hurdles for the study of T-reg cells and their involvement in human disease. The identification of the transcription factor Foxp3 as a molecular correlate for T-reg function offered the opportunity to directly identify T-reg cells, but until recently adequate reagents were not available. The tools promising the solution for this problem have emerged through the development of transgenic mice in which Foxp3 expression drives the production of fluorescent proteins, as well as the development of mAb that are able to identify Foxp3(+) cells by histology or flow cytometry. With these new tools, the mAb in particular, it will become possible for the first time to directly probe the participation of Foxp3(+) T-reg cells in human pathology in a quantitative fashion.
引用
收藏
页码:1678 / 1680
页数:3
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