Tracking epitope-specific T cells

被引:227
作者
Moon, James J. [1 ,2 ]
Chu, H. Hamlet [1 ,2 ]
Hataye, Jason [1 ,2 ]
Pagan, Antonio J. [1 ,2 ]
Pepper, Marion [1 ,2 ]
McLachlan, James B. [1 ,2 ]
Zell, Traci
Jenkins, Marc K. [1 ,2 ]
机构
[1] Univ Minnesota, Sch Med, Dept Microbiol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Ctr Immunol, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
CLASS-II TETRAMERS; EX-VIVO ANALYSIS; IN-VIVO; PRECURSOR FREQUENCY; FUNCTIONAL AVIDITY; PEPTIDE TETRAMERS; ANTIGEN-RECEPTOR; CLONAL EXPANSION; PERIPHERAL-BLOOD; IMMUNE-RESPONSE;
D O I
10.1038/nprot.2009.9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The tracking of antigen-specific T cells in vivo is a useful approach for the study of the adaptive immune response. This protocol describes how populations of T cells specific for a given peptide-major histocompatibility complex (pMHC) epitope can be tracked based solely on T-cell receptor (TCR) specificity as opposed to other indirect methods based on function. The methodology involves the adoptive transfer of TCR transgenic T cells with defined epitope specificity into histocompatible mice and the subsequent detection of these cells through the use of congenic or clonotypic markers. Alternatively, endogenous epitope-specific T cells can be tracked directly through the use of pMHC tetramers. Using magnetic bead-based enrichment and advanced multiparameter flow cytometry, populations as small as five epitope-specific T cells can be detected from the peripheral lymphoid organs of a mouse. The adoptive transfer procedure can be completed within 3 h, whereas analysis of epitope-specific cells from mice can be completed within 6 h.
引用
收藏
页码:565 / 581
页数:17
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