Flow-cytometric detection of vaccinia-induced memory effector CD4+, CD8+, and γδTCR+ T cells capable of antigen-specific expansion and effector functions

被引:33
作者
Abate, G
Eslick, J
Newman, FK
Frey, SE
Belshe, RB
Monath, TP
Hoft, DF
机构
[1] St Louis Univ, Dept Internal Med, St Louis, MO 63110 USA
[2] St Louis Univ, Dept Mol Microbiol & Immunol, St Louis, MO 63110 USA
[3] Acambis Inc, Cambridge, MA USA
关键词
D O I
10.1086/444423
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We developed a carboxyfluorescein succinimidyl ester ( CFSE)-based flow-cytometric assay that can detect different subsets of vaccinia-specific T cells capable of both antigen-specific expansion and protective effector functions. Proliferation and effector functions were detected by CFSE dilution and intracellular staining, respectively. Absolute numbers of CD4+/CFSE10/interferon (IFN)-gamma(+), CD8(+)/CFSE10/IFN-gamma(+), CD8(+)/CFSE10/granzyme A(+), and CD8(+)/CFSE10/CD107a(+) T cells present after in vitro stimulation with live vaccinia were significantly higher in immunized individuals (P < .05). These CD4(+) and CD8(+) T cell increases were 12 log higher than P <= .05 increases detectable by standard lymphoproliferation and cytotoxicity assays. Vaccinia-specific CD8(+)/CFSE10/ IFN-gamma(+) and granzyme A(+) T cell responses were significantly correlated with the results of standard Cr-51-release cytolytic assays (P < .05). Furthermore, vaccinia induced antigen-specific memory gamma delta T cells. We demonstrate P < .05 that vaccinia induces robust memory effector CD4(+), CD8(+), and gd T cells, all of which are relevant for protection against smallpox. CFSE-based flow-cytometric assays will be useful in evaluating cell-mediated immune responses induced by new smallpox vaccines.
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收藏
页码:1362 / 1371
页数:10
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