Sensitive and viable identification of antigen-specific CD8+T cells by a flow cytometric assay for degranulation

被引:1290
作者
Betts, MR [1 ]
Brenchley, JM [1 ]
Price, DA [1 ]
De Rosa, SC [1 ]
Douek, DC [1 ]
Roederer, M [1 ]
Koup, RA [1 ]
机构
[1] NIAID, Immunol Lab, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
关键词
degranulation; T lymphocyte; intraceflular cytokine; CD107a; CD107b;
D O I
10.1016/S0022-1759(03)00265-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Flow cytometric detection of antigen-specific CD8+ T cells has previously been limited to MHC-class I tetramer staining or intracellular cytokine production, neither of which measure the cytolytic potential of these cells. Here we present a novel technique to enumerate antigen-specific CD8+ T cells using a marker expressed on the cell surface following activation induced degranulation, a necessary precursor of cytolysis. This assay measures the exposure of CD107a and b, present in the membrane of cytotoxic granules, onto the cell surface as a result of degranulation. Acquisition of cell surface CD107a and In is associated with loss of intracellular perform and is inhibited by colchicine, indicating that exposure of CD107a and b to the cell surface is dependent on degranulation. CD107a and b are expressed on the cell surface of CD8+ T cells following activation with cognate peptide, concordant with production of intracellular IFNgamma. Finally, CD107-expressing CD8+ T cells are shown to mediate cytolytic activity in an antigen-specific manner. Measurement of CD107a and b expression can also be combined with MHC-class I tetramer labeling and intracellular cytokine staining to provide a more complete assessment of the functionality of CD8+ T cells expressing cognate T cell receptors (TCR). (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:65 / 78
页数:14
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