机构:
Univ Iowa, Grad Program Immunol, Dept Microbiol & Interdisciplinary, Iowa City, IA 52242 USAUniv Iowa, Grad Program Immunol, Dept Microbiol & Interdisciplinary, Iowa City, IA 52242 USA
Harty, John T.
[1
]
Badovinac, Vladimir P.
论文数: 0引用数: 0
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机构:
Univ Iowa, Dept Pathol, Iowa City, IA 52242 USAUniv Iowa, Grad Program Immunol, Dept Microbiol & Interdisciplinary, Iowa City, IA 52242 USA
Badovinac, Vladimir P.
[2
]
机构:
[1] Univ Iowa, Grad Program Immunol, Dept Microbiol & Interdisciplinary, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Pathol, Iowa City, IA 52242 USA
The ability to develop and sustain populations of memory T cells after infection or immunization is a hallmark of the adaptive immune response and a basis for protective vaccination against infectious disease. Technical advances that allow direct ex vivo identification and characterization of antigen-specific CD8(+) T cells at various stages of the response to infection or vaccination in mouse models have fuelled efforts to characterize the factors that control memory CD8(+) T-cell generation. Here, we dissect the input signals that shape the characteristics of the memory CD8(+) T-cell response and discuss how manipulation of these signals has the potential to reshape CD8(+) T-cell memory and improve the efficacy of vaccination.