Molecular pathways regulating CD4+ T cell differentiation, anergy and memory with implications for vaccines

被引:33
作者
Ahlers, Jeffrey D. [1 ]
Belyakov, Igor M. [2 ]
机构
[1] NIAID, NIH, Bethesda, MD 20817 USA
[2] Midwest Res Inst, Frederick, MD 21702 USA
关键词
HUMAN DENDRITIC CELLS; ARYL-HYDROCARBON RECEPTOR; GROWTH-FACTOR-BETA; HUMAN TH17 CELLS; ROR-GAMMA-T; IN-VIVO; TRANSCRIPTION FACTOR; CUTTING EDGE; LINEAGE COMMITMENT; HELPER-CELLS;
D O I
10.1016/j.molmed.2010.07.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
CD4(+) T cells occupy a central role in the induction and regulation of adaptive immune responses. Activated CD4(+) T helper (Th) cells exert immediate effector functions by producing cytokines and chemokines, providing help for the induction of CD8(+) cytotoxic T lymphocyte responses and memory, and providing help for immunoglobulin class switching, affinity maturation of antibody and B cell memory. Inherent in naive CD4(+) T cells is the flexibility to adopt alternate lineage potentials, which depend upon regulatory mechanisms that change with tissue microenvironment and upon infection. Here, we discuss lineage instructive programs that regulate CD4(+) T cell differentiation and memory and how to translate this knowledge into vaccines and immunotherapies that promote protective immune responses.
引用
收藏
页码:478 / 491
页数:14
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