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Immunologic considerations for generating memory CD8 T cells through vaccination
被引:59
|作者:
Butler, Noah S.
[1
]
Nolz, Jeffrey C.
[1
]
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
关键词:
HUMAN-IMMUNODEFICIENCY-VIRUS;
IL-7;
RECEPTOR-ALPHA;
CLONAL EXPANSION;
CUTTING EDGE;
SECONDARY RESPONSES;
NONLYMPHOID TISSUE;
IN-VIVO;
EFFECTOR;
IMMUNITY;
EXPRESSION;
D O I:
10.1111/j.1462-5822.2011.01594.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
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.
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页码:925 / 933
页数:9
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