Ex vivo characterization of allo-MHC-restricted T cells specific for a single MHC-peptide complex

被引:21
作者
Pittet, MJ
Gati, A
Le Gal, FA
Bioley, G
Guillaume, P
de Smedt, M
Plum, J
Speiser, DE
Cerottini, JC
Dietrich, PY
Romero, P
Zippelius, A
机构
[1] Univ Hosp Zurich, Dept Oncol, CH-8091 Zurich, Switzerland
[2] Univ Hosp, Ludwig Inst Canc Res, Div Clin Oncoimmunol, Lausanne, Switzerland
[3] Univ Hosp, Lab Tumor Immunol, Div Oncol, Geneva, Switzerland
[4] Univ Lausanne, Lausanne Branch, Ludwig Inst Canc Res, Epalinges, Switzerland
[5] Univ Hosp, Dept Clin Chem Microbiol & Immunol, Ghent, Belgium
关键词
D O I
10.4049/jimmunol.176.4.2330
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Alloreactive T cells are thought to be a potentially rich source of high-avidity T cells with therapeutic potential since tolerance to self-Ags is restricted to self-MHC recognition. Given the particularly high frequency of alloreactive T cells in the peripheral immune system, we used numerous MHC class I multimers to directly visualize and isolate viral and tumor Ag-specific alloreactive CD8 T cells. In fact, all but one specificities screened were undetectable in ex vivo labeling. In this study, we report the occurrence of CD8 T cells specifically labeled with allo-HLA-A*0201/Melan-A/MART-1(26-35) multimers at frequencies that are in the range of 10(-4) CD8 T cells and are thus detectable ex vivo by flow cytometry. We report the thymic generation and shaping of tumor Ag-specific, alloreactive T cells as well as their fate once seeded in the periphery. We show that these cells resemble their counterparts in HLA-A*0201-positive individuals, based on their structural and functional attributes. The Journal of Immunology, 2006, 176: 2330-2336.
引用
收藏
页码:2330 / 2336
页数:7
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