Technical advancement in regulatory T cell isolation and characterization using CD127 expression in patients with malignant glioma treated with autologous dendritic cell vaccination

被引:18
作者
Ardon, H. [1 ,2 ]
Verbinnen, B. [2 ]
Maes, W. [2 ]
Beez, T. [2 ,3 ]
Van Cool, S. [2 ,4 ]
De Vleeschouwer, S. [1 ,2 ]
机构
[1] Univ Hosp Leuven, Dept Neurosurg, B-3000 Louvain, Belgium
[2] Univ Hosp Leuven, Expt Immunol Lab, B-3000 Louvain, Belgium
[3] Univ Hosp Heinrich Heine, Inst Transplantat Diagnost & Cell Therapeut, Dusseldorf, Germany
[4] Univ Hosp Leuven, Dept Paediat, B-3000 Louvain, Belgium
关键词
Glioma; DC vaccination; Monitoring; Treg; Foxp3; CD127; FOXP3;
D O I
10.1016/j.jim.2009.10.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have successfully treated over two hundred high-grade glioma (HGG) patients with immunotherapy consisting of vaccination with autologous dendritic cells (DCs) loaded with autologous tumour lysate. It has been documented that regulatory T cells (Treg) can counteract anti-tumour immune responses. Therefore, monitoring of Treg in these patients is essential. Up till now, Treg have been characterized based on the expression of the transcription factor Foxp3. Here, we validated IL-7 receptor alpha subunit (CD127)dim expression as a marker for human Treg within HGG patients, as a less laborious assay for routine use in tumour vaccination trials. We noted a strong positive correlation between Foxp3 expression and CD127dim expression in CD4 + CD25+ and CD4+ cells. The suppressive function of CD4 + CD127dim cells was assessed in an allogeneic mixed lymphocyte reaction (MLR). We conclude that CD127 staining is a fast, well-suited and reproducible Treg monitoring tool in HGG patients treated with immunotherapy. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 173
页数:5
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