Metabolic control of dendritic cell activation and function: recent advances and clinical implications

被引:116
作者
Everts, Bart [1 ,2 ]
Pearce, Edward J. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[2] Leiden Univ, Med Ctr, Dept Parasitol, Leiden, Netherlands
来源
FRONTIERS IN IMMUNOLOGY | 2014年 / 5卷
基金
美国国家卫生研究院;
关键词
metabolism; oxidative phosphorylation; mitochondria; glycolysis; TLR signaling; immunogenic dendritic cells; tolerogenic dendritic cells; immunotherapy; MAMMALIAN TARGET; NITRIC-OXIDE; RAPAMYCIN; DIFFERENTIATION; MTOR; RESVERATROL; INFLAMMATION; MACROPHAGES; INHIBITION; IMPROVES;
D O I
10.3389/fimmu.2014.00203
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) are key regulators of both immunity and tolerance by controlling activation and polarization of effector T helper cell and regulatory T cell responses. Therefore, there is a major focus on developing approaches to manipulate DC function for immunotherapy. It is well known that changes in cellular activation are coupled to profound changes in cellular metabolism. Over the past decade there is a growing appreciation that these metabolic changes also underlie the capacity of immune cells to perform particular functions. This has led to the concept that the manipulation of cellular metabolism can be used to shape innate and adaptive immune responses. While most of our understanding in this area has been gained from studies with T cells and macrophages, evidence is emerging that the activation and function of DCs are also dictated by the type of metabolism these cells commit to. We here discuss these new insights and explore whether targeting of metabolic pathways in DCs could hold promise as a novel approach to manipulate the functional properties of DCs for clinical purposes.
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页数:7
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