Mapping T cell epitopes by flow cytometry

被引:63
作者
Hoffmeister, B
Kiecker, F
Tesfa, L
Volk, HD
Picker, LJ
Kern, F
机构
[1] Humboldt Univ, Charite, Dept Med Immunol, D-10117 Berlin, Germany
[2] Oregon Hlth Sci Univ, Vaccine & Gene Therapy Inst, Portland, OR 97201 USA
关键词
VACCINATION; INFECTION; SUBSETS;
D O I
10.1016/S1046-2023(02)00349-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Epitope mapping by flow cytometry is a very modern approach that not only identifies T-cell epitopes but simultaneously allows for detailed analysis of the responding T-cell subsets including lineage, activation marker expression, and other markers of interest. The most frequently used approach is based on the identification of intracellular cytokines in secretion-inhibited activated T cells following stimulation with peptides or peptide pools. A more recently developed assay analyzes T-cell proliferation by measuring the decrease in carboxyfluorescein diacetate succinimidyl ester staining in proliferated cells. This article includes information on peptide configuration, a section on the design and efficient application of peptide pools, and working laboratory protocols for both assays. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:270 / 281
页数:12
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