| Literature DB >> 18468462 |
Joseph D Miller1, Robbert G van der Most, Rama S Akondy, John T Glidewell, Sophia Albott, David Masopust, Kaja Murali-Krishna, Patryce L Mahar, Srilatha Edupuganti, Susan Lalor, Stephanie Germon, Carlos Del Rio, Mark J Mulligan, Silvija I Staprans, John D Altman, Mark B Feinberg, Rafi Ahmed.
Abstract
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.Entities:
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Year: 2008 PMID: 18468462 DOI: 10.1016/j.immuni.2008.02.020
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745