Miller Joseph D, van der Most Robbert G, Akondy Rama S, Glidewell John T, Albott Sophia, Masopust David, Murali-Krishna Kaja, Mahar Patryce L, Edupuganti Srilatha, Lalor Susan, Germon Stephanie, Del Rio Carlos, Mulligan Mark J, Staprans Silvija I, Altman John D, Feinberg Mark B, Ahmed Rafi
Emory Vaccine Center and the Hope Clinic, Emory University School of Medicine, Atlanta, GA 30322, USA.
Immunity. 2008 May;28(5):710-22. doi: 10.1016/j.immuni.2008.02.020. Epub 2008 May 8.
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.
为了探究人类T细胞对急性病毒感染的反应,我们对针对活黄热病病毒和天花疫苗(两种非常成功的人类疫苗)的CD8(+) T细胞进行了纵向分析。我们的结果表明,两种疫苗都产生了强烈的初级效应CD8(+) T细胞反应,其规模相当大,可用一组简单的四个表型标志物轻松定量。其次,疫苗诱导的T细胞反应具有高度特异性,旁观者效应最小。第三,病毒特异性CD8(+) T细胞经历了一个必经的效应阶段,收缩超过90%,并逐渐分化为长寿记忆细胞。最后,这些记忆细胞功能高度活跃,经历了一个与针对持续性病毒的人类CD8(+) T细胞所描述的记忆分化程序不同的程序。这些结果为有史以来开发的两种最有效疫苗所诱导的CD8(+) T细胞反应提供了一个基准。