Immunologic considerations for generating memory CD8 T cells through vaccination
被引:59
作者:
Butler, Noah S.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USAUniv Iowa, Dept Microbiol, Iowa City, IA 52242 USA
Butler, Noah S.
[1
]
Nolz, Jeffrey C.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USAUniv Iowa, Dept Microbiol, Iowa City, IA 52242 USA
Nolz, Jeffrey C.
[1
]
Harty, John T.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA
Univ Iowa, Dept Pathol, Iowa City, IA 52242 USA
Univ Iowa, Interdisciplinary Grad Program Immunol, Iowa City, IA 52242 USAUniv Iowa, Dept Microbiol, Iowa City, IA 52242 USA
Harty, John T.
[1
,2
,3
]
机构:
[1] Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Pathol, Iowa City, IA 52242 USA
[3] Univ Iowa, Interdisciplinary Grad Program Immunol, Iowa City, IA 52242 USA
Following infection or vaccination, naive CD8 T cells that receive the appropriate integration of antigenic, co-stimulatory and inflammatory signals undergo a programmed series of biological changes that ultimately results in the generation of memory cells. Memory CD8 T cells, in contrast to naive cells, more effectively limit or prevent pathogen re-infection because of both qualitative and quantitative changes that occur following their induction. Unlike vaccination strategies aimed at generating antibody production, the ability to generate protective memory CD8 T cells has proven more complicated and problematic. However, recent experimental results have revealed important principles regarding the molecular and genetic basis for memory CD8 T cell formation, as well as identified ways to manipulate their development through vaccination, resulting in potential new avenues to enhance protective immunity.