共 72 条
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.
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页码:565 / 581
页数:17
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