Anergic T Cells Are Metabolically Anergic

被引:213
作者
Zheng, Yan [1 ]
Delgoffe, Greg M. [1 ]
Meyer, Christian F. [1 ]
Chan, Waipan [1 ]
Powell, Jonathan D. [1 ]
机构
[1] Johns Hopkins Sch Med, Sidney Kimmel Canc Res Ctr, Baltimore, MD 21231 USA
基金
美国国家卫生研究院;
关键词
ACTIVATED PROTEIN-KINASE; CLONAL ANERGY; MAMMALIAN TARGET; DENDRITIC CELLS; MTOR; EXPRESSION; INDUCTION; TOLERANCE; PATHWAYS; ARREST;
D O I
10.4049/jimmunol.0803510
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Full T cell activation requires TCR engagement (signal 1) in the context of costimulation (signal 2). Costimulation is required for maximal expression of effector cytokines and prevention of T cell anergy. It has become increasingly clear that another major function of costimulation is to up-regulate the metabolic machinery necessary for T cell function. In this report we demonstrate that anergic T cells are metabolically anergic, in that upon full stimulation (signals 1 plus 2) they fail to up-regulate the machinery necessary to support increased metabolism. These findings suggest that one mechanism responsible for the maintenance of T cell anergy is failure to up-regulate the metabolic machinery. Furthermore, we demonstrate that by blocking leucine, glucose, and energy metabolism, T cell activation is mitigated. Additionally, inhibition of these metabolic pathways during T cell activation leads to anergy in Th1-differentiated cells. Overall, our findings extend the role of T cell metabolism in regulating T cell function. The Journal of Immunology, 2009, 183: 6095-6101.
引用
收藏
页码:6095 / 6101
页数:7
相关论文
共 32 条
[1]   The novel cyclophilin binding compound, sanglifehrin A, disassociates G1 cell cycle arrest from tolerance induction [J].
Allen, A ;
Zheng, Y ;
Gardner, L ;
Safford, M ;
Horton, MR ;
Powell, JD .
JOURNAL OF IMMUNOLOGY, 2004, 172 (08) :4797-4803
[2]   Antigen-presenting dendritic cells provide the reducing extracellular microenvironment required for T lymphocyte activation [J].
Angelini, G ;
Gardella, S ;
Ardy, M ;
Ciriolo, MR ;
Filomeni, G ;
Di Trapani, G ;
Clarke, F ;
Sitia, R ;
Rubartelli, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (03) :1491-1496
[3]   REVERSAL OF INVITRO T-CELL CLONAL ANERGY BY IL-2 STIMULATION [J].
BEVERLY, B ;
KANG, SM ;
LENARDO, MJ ;
SCHWARTZ, RH .
INTERNATIONAL IMMUNOLOGY, 1992, 4 (06) :661-671
[4]   Glucose deprivation inhibits multiple key gene expression events and effector functions in CD8+ T cells [J].
Cham, Candace M. ;
Driessens, Gregory ;
O'Keefe, James P. ;
Gajewski, Thomas F. .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2008, 38 (09) :2438-2450
[5]   Infectious tolerance via the consumption of essential amino acids and mTOR signaling [J].
Cobbold, Stephen P. ;
Adams, Elizabeth ;
Farquhar, Claire A. ;
Nolan, Kathleen F. ;
Howie, Duncan ;
Lui, Kathy O. ;
Fairchild, Paul J. ;
Mellor, Andrew L. ;
Ron, David ;
Waldmann, Herman .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (29) :12055-12060
[6]   Clonal anergy is maintained independently of T cell proliferation [J].
Colombetti, S ;
Benigni, F ;
Basso, V ;
Mondino, A .
JOURNAL OF IMMUNOLOGY, 2002, 169 (11) :6178-6186
[7]   Fuel feeds function: Energy metabolism and the T-cell response [J].
Fox, CJ ;
Hammerman, PS ;
Thompson, CB .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (11) :844-852
[8]   Regulation of T lymphocyte metabolism [J].
Frauwirth, KA ;
Thompson, CB .
JOURNAL OF IMMUNOLOGY, 2004, 172 (08) :4661-4665
[9]   Failure at the effector phase: Immune barriers at the level of the melanoma tumor microenvironment [J].
Gajewski, Thomas F. .
CLINICAL CANCER RESEARCH, 2007, 13 (18) :5256-5261
[10]  
Harris Thurl E, 2003, Sci STKE, V2003, pre15