Human effector and memory CD8+ T cell responses to smallpox and yellow fever vaccines

被引:478
作者
Miller, Joseph D. [1 ,2 ]
van der Most, Robbert G. [1 ,2 ]
Akondy, Rama S. [1 ,2 ]
Glidewell, John T. [1 ,2 ]
Albott, Sophia [1 ,2 ]
Masopust, David [1 ,2 ]
Murali-Krishna, Kaja [1 ,2 ]
Mahar, Patryce L. [1 ,2 ]
Edupuganti, Srilatha [1 ,2 ]
Lalor, Susan [1 ,2 ]
Germon, Stephanie [1 ,2 ]
Del Rio, Carlos [1 ,2 ]
Mulligan, Mark J. [1 ,2 ]
Staprans, Silvija I. [1 ,2 ]
Altman, John D. [1 ,2 ]
Feinberg, Mark B. [1 ,2 ]
Ahmed, Rafi [1 ,2 ]
机构
[1] Emory Univ, Sch Med, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Hope Clin, Atlanta, GA 30322 USA
关键词
D O I
10.1016/j.immuni.2008.02.020
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To explore the human T cell response to acute viral infection, we performed a longitudinal analysis of CD8(+) T cells responding to the live yellow fever virus and smallpox vaccines-two highly successful human vaccines. Our results show that both vaccines generated a brisk primary effector CD8(+) T cell response of substantial magnitude that could be readily quantitated with a simple set of four phenotypic markers. Secondly, the vaccine-induced T cell response was highly specific with minimal bystander effects. Thirdly, virus-specific CD8(+) T cells passed through an obligate effector phase, contracted more than 90% and gradually differentiated into long-lived memory cells. Finally, these memory cells were highly functional and underwent a memory differentiation program distinct from that described for human CD8(+) T cells specific for persistent viruses. These results provide a benchmark for CD8(+) T cell responses induced by two of the most effective vaccines ever developed.
引用
收藏
页码:710 / 722
页数:13
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