Defining the molecular blueprint that drives CD8+ T cell differentiation in response to infection

被引:15
作者
Russ, Brendan E. [1 ]
Denton, Alice E. [2 ]
Hatton, Lauren [1 ]
Croom, Hayley [1 ]
Olson, Matthew R. [1 ]
Turner, Stephen J. [1 ]
机构
[1] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3010, Australia
[2] Univ Cambridge, Cambridge Res Inst, Dept Med, Cambridge, England
来源
FRONTIERS IN IMMUNOLOGY | 2012年 / 3卷
关键词
cytotoxic T cells; memory T cells; transcription factors; epigenetics; histone modifications; TRANSCRIPTION FACTOR; EFFECTOR FUNCTION; CUTTING EDGE; CHROMATIN SIGNATURES; EARLY ESTABLISHMENT; RECALL RESPONSES; CLONAL EXPANSION; DENDRITIC CELLS; RNA-POLYMERASE; CENTRAL MEMORY;
D O I
10.3389/fimmu.2012.00371
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A cardinal feature of adaptive, cytotoxic T lymphocyte (CTL)-mediated immunity is the ability of naive CTLs to undergo a program of differentiation and proliferation upon activation resulting in the acquisition of lineage-specific T cell functions and eventual establishment of immunological memory. In this review, we examine the molecular factors that shape both the acquisition and maintenance of lineage-specific effector function in virus-specific CTL during both the effector and memory phases of immunity.
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页数:11
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