T regulatory cells metabolism: The influence on functional properties and treatment potential

被引:10
作者
Tomaszewicz, Martyna [1 ,2 ]
Ronowska, Anna [3 ]
Zielinski, Maciej [1 ,2 ]
Jankowska-Kulawy, Agnieszka [3 ]
Trzonkowski, Piotr [1 ,2 ]
机构
[1] Med Univ Gdansk, Fac Med, Dept Med Immunol, Gdanisk, Poland
[2] Poltreg SA, Gdanisk, Poland
[3] Med Univ Gdansk, Fac Med, Dept Lab Med, Gdanisk, Poland
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
metabolism; autoimmunity; glycolysis; fatty acid oxidation; mTOR; ischemia; mitochondria; adenosine; KAPPA-B; ECTONUCLEOTIDASE CD39; MOLECULAR-MECHANISMS; ENERGY-METABOLISM; DENDRITIC CELLS; DOUBLE-BLIND; CANCER; RECEPTOR; MTOR; DIFFERENTIATION;
D O I
10.3389/fimmu.2023.1122063
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4(+)CD25(high)FoxP3(+) regulatory T cells (Tregs) constitute a small but substantial fraction of lymphocytes in the immune system. Tregs control inflammation associated with infections but also when it is improperly directed against its tissues or cells. The ability of Tregs to suppress (inhibit) the immune system is possible due to direct interactions with other cells but also in a paracrine fashion via the secretion of suppressive compounds. Today, attempts are made to use Tregs to treat autoimmune diseases, allergies, and rejection after bone marrow or organ transplantation. There is strong evidence that the metabolic program of Tregs is connected with the phenotype and function of these cells. A modulation towards a particular metabolic stage of Tregs may improve or weaken cells' stability and function. This may be an essential tool to drive the immune system keeping it activated during infections or suppressed when autoimmunity occurs.
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页数:11
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