Metabolic control of the Treg/Th17 axis

被引:173
作者
Barbi, Joseph [1 ]
Pardoll, Drew [1 ]
Pan, Fan [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Oncol, Immunol & Hematopoiesis Div,Sidney Kimmel Compreh, Baltimore, MD 21205 USA
关键词
Th17; Treg; metabolism; T-cell differentiation; PROLIFERATOR-ACTIVATED-RECEPTOR; HYPOXIA-INDUCIBLE FACTOR; REGULATORY T-CELLS; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; GAMMA AGONISTS INHIBIT; ACID-BINDING PROTEINS; PPAR-GAMMA; TH17; DIFFERENTIATION; MAMMALIAN TARGET; CUTTING EDGE;
D O I
10.1111/imr.12029
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The interplay of the immune system with other aspects of physiology is continually being revealed and in some cases studied in considerable mechanistic detail. A prime example is the influence of metabolic cues on immune responses. It is well appreciated that upon activation, T cells take on a metabolic profile profoundly distinct from that of their quiescent and anergic counterparts; however, a number of recent breakthroughs have greatly expanded our knowledge of how aspects of cellular metabolism can shape a T-cell response. Particularly important are findings that certain environmental cues can tilt the delicate balance between inflammation and immune tolerance by skewing T-cell fate decisions toward either the T-helper 17 (Th17) or T-regulatory (Treg) cell lineage. Recognizing the unappreciated immune-modifying potential of metabolic factors and particularly those involved in the generation of these functionally opposing T-cell subsets will likely add new and potent therapies to our repertoire for treating immune mediated pathologies. In this review, we summarize and discuss recent findings linking certain metabolic pathways, enzymes, and by-products to shifts in the balance between Th17 and Treg cell populations. These advances highlight numerous opportunities for immune modulation.
引用
收藏
页码:52 / 77
页数:26
相关论文
共 191 条
[1]   Peroxisome proliferator activated receptor γ in colonic epithelial cells protects against experimental inflammatory bowel disease [J].
Adachi, M. ;
Kurotani, R. ;
Morimura, K. ;
Shah, Y. ;
Sanford, M. ;
Madison, B. B. ;
Gumucio, D. L. ;
Marin, H. E. ;
Peters, J. M. ;
Young, H. A. ;
Gonzalez, F. J. .
GUT, 2006, 55 (08) :1104-1113
[2]   IDO Activates Regulatory T Cells and Blocks Their Conversion into Th17-Like T Cells [J].
Baban, Babak ;
Chandler, Phillip R. ;
Sharma, Madhav D. ;
Pihkala, Jeanene ;
Koni, Pandelakis A. ;
Munn, David H. ;
Mellor, Andrew L. .
JOURNAL OF IMMUNOLOGY, 2009, 183 (04) :2475-2483
[3]   Role of regulatory T cells and FOXP3 in human diseases [J].
Bacchetta, Rosa ;
Gambineri, Eleonora ;
Roncarolo, Maria-Grazia .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2007, 120 (02) :227-235
[4]   AMPK agonist downregulates innate and adaptive immune responses in TNBS-induced murine acute and relapsing colitis [J].
Bai, Aiping ;
Ma, Allan G. ;
Yong, Michael ;
Weiss, Carolyn R. ;
Ma, Yanbing ;
Guan, Qingdong ;
Bernstein, Charles N. ;
Peng, Zhikang .
BIOCHEMICAL PHARMACOLOGY, 2010, 80 (11) :1708-1717
[5]   Novel Anti-Inflammatory Action of 5-Aminoimidazole-4-carboxamide Ribonucleoside with Protective Effect in Dextran Sulfate Sodium-Induced Acute and Chronic Colitis [J].
Bai, Aiping ;
Yong, Michael ;
Ma, Allan G. ;
Ma, Yanbing ;
Weiss, Carolyn R. ;
Guan, Qingdong ;
Bernstein, Charles N. ;
Peng, Zhikang .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2010, 333 (03) :717-725
[6]   Regulatory T Cells Reinforce Intestinal Homeostasis [J].
Barnes, Michael J. ;
Powrie, Fiona .
IMMUNITY, 2009, 31 (03) :401-411
[7]   Activation rules: the two-signal theories of immune activation [J].
Baxter, AG ;
Hodgkin, PD .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (06) :439-446
[8]   SREBP in signal transduction: cholesterol metabolism and beyond [J].
Bengoechea-Alonso, Maria T. ;
Ericsson, Johan .
CURRENT OPINION IN CELL BIOLOGY, 2007, 19 (02) :215-222
[9]   Topotecan blocks hypoxia-inducible factor-1α, and vascular endothelial growth factor expression induced by insulin-like growth factor-I in neuroblastoma cells [J].
Beppu, Y ;
Nakamura, K ;
Linehan, WM ;
Rapisarda, A ;
Thiele, CJ .
CANCER RESEARCH, 2005, 65 (11) :4775-4781
[10]  
Bergamini G, 2012, NAT CHEM BIOL, V8, P576, DOI [10.1038/nchembio.957, 10.1038/NCHEMBIO.957]