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
[21]   Vitamin D Suppresses Th17 Cytokine Production by Inducing C/EBP Homologous Protein (CHOP) Expression [J].
Chang, Seon Hee ;
Chung, Yeonseok ;
Dong, Chen .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (50) :38751-38755
[22]   Insulin Resistance and Altered Systemic Glucose Metabolism in Mice Lacking Nur77 [J].
Chao, Lily C. ;
Wroblewski, Kevin ;
Zhang, Zidong ;
Pei, Liming ;
Vergnes, Laurent ;
Ilkayeva, Olga R. ;
Ding, Shi Ying ;
Reue, Karen ;
Watt, Matthew J. ;
Newgard, Christopher B. ;
Pilch, Paul F. ;
Hevener, Andrea L. ;
Tontonoz, Peter .
DIABETES, 2009, 58 (12) :2788-2796
[23]   Nur77 activated by hypoxia-inducible factor-1α overproduces proopiomelanocortin in von Hippel-Lindau-mutated renal cell carcinoma [J].
Choi, JW ;
Park, SC ;
Kang, GH ;
Liu, JO ;
Youn, HD .
CANCER RESEARCH, 2004, 64 (01) :35-39
[24]   PPAR-γ is a major driver of the accumulation and phenotype of adipose tissue Treg cells [J].
Cipolletta, Daniela ;
Feuerer, Markus ;
Li, Amy ;
Kamei, Nozomu ;
Lee, Jongsoon ;
Shoelson, Steven E. ;
Benoist, Christophe ;
Mathis, Diane .
NATURE, 2012, 486 (7404) :549-U151
[25]   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
[26]   Hypoxia: an alarm signal during intestinal inflammation [J].
Colgan, Sean P. ;
Taylor, Cormac T. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2010, 7 (05) :281-287
[27]   Innate IL-17-producing cells: the sentinels of the immune system [J].
Cua, Daniel J. ;
Tato, Cristina M. .
NATURE REVIEWS IMMUNOLOGY, 2010, 10 (07) :479-489
[28]   Liver X receptor (LXR) mediates negative regulation of mouse and human Th17 differentiation [J].
Cui, Guoliang ;
Qin, Xia ;
Wu, Lili ;
Zhang, Yuebo ;
Sheng, Xiaoyan ;
Yu, Qiwen ;
Sheng, Hongguang ;
Xi, Beili ;
Zhang, Jingwu Z. ;
Zang, Ying Qin .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (02) :658-670
[29]   The Link between the PDL1 Costimulatory Pathway and Th17 in Fetomaternal Tolerance [J].
D'Addio, Francesca ;
Riella, Leonardo V. ;
Mfarrej, Bechara G. ;
Chabtini, Lola ;
Adams, La Tonya ;
Yeung, Melissa ;
Yagita, Hideo ;
Azuma, Miyuki ;
Sayegh, Mohamed H. ;
Guleria, Indira .
JOURNAL OF IMMUNOLOGY, 2011, 187 (09) :4530-4541
[30]   The interplay between MYC and HIF in the Warburg effect [J].
Dang, C. V. .
ONCOGENES MEET METABOLISM: FROM DEREGULATED GENES TO A BROADER UNDERSTANDING OF TUMOUR PHYSIOLOGY, 2008, 4 :35-53