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本文引用的文献

1
The energy sensor AMPK regulates T cell metabolic adaptation and effector responses in vivo.能量传感器 AMPK 调节体内 T 细胞代谢适应性和效应器反应。
Immunity. 2015 Jan 20;42(1):41-54. doi: 10.1016/j.immuni.2014.12.030. Epub 2015 Jan 2.
2
Akt inhibition enhances expansion of potent tumor-specific lymphocytes with memory cell characteristics.Akt 抑制增强了具有记忆细胞特征的强效肿瘤特异性淋巴细胞的扩增。
Cancer Res. 2015 Jan 15;75(2):296-305. doi: 10.1158/0008-5472.CAN-14-2277. Epub 2014 Nov 28.
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De novo fatty acid synthesis controls the fate between regulatory T and T helper 17 cells.从头合成脂肪酸控制调节性 T 细胞和辅助性 T 细胞 17 命运的抉择。
Nat Med. 2014 Nov;20(11):1327-33. doi: 10.1038/nm.3704. Epub 2014 Oct 5.
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Bispecific antibody platforms for cancer immunotherapy.双特异性抗体平台在癌症免疫治疗中的应用。
Crit Rev Oncol Hematol. 2014 Dec;92(3):153-65. doi: 10.1016/j.critrevonc.2014.08.003. Epub 2014 Aug 20.
5
Serendipity and the discovery of novel compounds that restore mitochondrial plasticity.意外发现与恢复线粒体可塑性的新型化合物的发现
Clin Pharmacol Ther. 2014 Dec;96(6):672-83. doi: 10.1038/clpt.2014.174. Epub 2014 Sep 4.
6
Anaplerotic metabolism of alloreactive T cells provides a metabolic approach to treat graft-versus-host disease.同种异体反应性T细胞的回补代谢为治疗移植物抗宿主病提供了一种代谢方法。
J Pharmacol Exp Ther. 2014 Nov;351(2):298-307. doi: 10.1124/jpet.114.218099. Epub 2014 Aug 14.
7
The Intercellular Metabolic Interplay between Tumor and Immune Cells.肿瘤细胞与免疫细胞的细胞间代谢相互作用。
Front Immunol. 2014 Jul 28;5:358. doi: 10.3389/fimmu.2014.00358. eCollection 2014.
8
Mechanistic target of rapamycin inhibition extends cellular lifespan in dendritic cells by preserving mitochondrial function.雷帕霉素作用机制靶点的抑制通过维持线粒体功能来延长树突状细胞的细胞寿命。
J Immunol. 2014 Sep 15;193(6):2821-30. doi: 10.4049/jimmunol.1302498. Epub 2014 Aug 8.
9
Biochemical signaling of PD-1 on T cells and its functional implications.T细胞上PD-1的生化信号传导及其功能意义。
Cancer J. 2014 Jul-Aug;20(4):265-71. doi: 10.1097/PPO.0000000000000059.
10
The growing landscape of lysine acetylation links metabolism and cell signalling.赖氨酸乙酰化修饰将代谢与细胞信号联系起来的研究现状。
Nat Rev Mol Cell Biol. 2014 Aug;15(8):536-50. doi: 10.1038/nrm3841.

靶向T细胞代谢进行治疗。

Targeting T cell metabolism for therapy.

作者信息

O'Sullivan David, Pearce Erika L

机构信息

Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, 63110, USA.

Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, 63110, USA.

出版信息

Trends Immunol. 2015 Feb;36(2):71-80. doi: 10.1016/j.it.2014.12.004. Epub 2015 Jan 15.

DOI:10.1016/j.it.2014.12.004
PMID:25601541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4323623/
Abstract

In the past several years a wealth of evidence has emerged illustrating how metabolism supports many aspects of T cell biology, as well as how metabolic changes drive T cell differentiation and fate. We outline developing principles in the regulation of T cell metabolism, and discuss how these processes are affected in settings of inflammation and cancer. In this context we discuss how metabolic pathways might be manipulated for the treatment of human disease, including how metabolism may be targeted to prevent T cell dysfunction in inhospitable microenvironments, to generate more effective adoptive cellular immunotherapies in cancer, and to direct T cell differentiation and function towards non-pathogenic phenotypes in settings of autoimmunity.

摘要

在过去几年中,大量证据表明新陈代谢如何支持T细胞生物学的多个方面,以及代谢变化如何驱动T细胞分化和命运。我们概述了T细胞代谢调节中的发展原则,并讨论了这些过程在炎症和癌症环境中是如何受到影响的。在此背景下,我们讨论了如何操纵代谢途径来治疗人类疾病,包括如何针对代谢以防止T细胞在恶劣微环境中功能失调,如何在癌症中产生更有效的过继性细胞免疫疗法,以及如何在自身免疫环境中将T细胞分化和功能导向非致病性表型。