Acidity-mediated induction of FoxP3+ regulatory T cells

被引:17
作者
Rao, Disha [1 ]
Stunnenberg, Johanna A. A. [1 ]
Lacroix, Ruben [1 ]
Dimitriadis, Petros [1 ]
Kaplon, Joanna [2 ]
Verburg, Fabienne [1 ]
van van Royen, Paula T. T. [1 ]
Hoefsmit, Esmee P. [1 ]
Renner, Kathrin [3 ,4 ]
Blank, Christian U. U. [1 ,5 ,6 ]
Peeper, Daniel S. S. [1 ,7 ]
机构
[1] Netherlands Canc Inst, Dept Mol Oncol & Immunol, Plesmanlaan 121, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst, Dept Clin Chem, Amsterdam, Netherlands
[3] Univ Hosp Regensburg, Dept Internal Med Hematol & Med Oncol 3, Regensburg, Germany
[4] Univ Hosp Regensburg, Dept Otorhinolaryngol, Regensburg, Germany
[5] Netherlands Canc Inst, Dept Med Oncol, Amsterdam, Netherlands
[6] Leiden Univ, Med Ctr, Dept Internal Med, Leiden, Netherlands
[7] Oncode Inst, Utrecht, Netherlands
关键词
Lactic acid; Regulatory T cells; Treg metabolism; Tumor microenvironment; LACTIC-ACID; TGF-BETA; TUMOR; METABOLISM; EXPRESSION; CANCER; CHECKPOINT; CONVERSION; RESPONSES; STRESS;
D O I
10.1002/eji.202250258
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Glucose limitation and increased lactic acid levels are consequences of the elevated glycolytic activity of tumor cells, and constitute a metabolic barrier for the function of tumor infiltrating effector immune cells. The immune-suppressive functions of regulatory T cells (Tregs) are unobstructed in lactic-acid rich environments. However, the impact of lactic acid on the induction of Tregs remains unknown. We observed increased TGF beta-mediated induction of Forkhead box P3(+) (FoxP3(+)) cells in the presence of extracellular lactic acid, in a glycolysis-independent, acidity-dependent manner. These CD4(+) FoxP3(+) cells expressed Treg-associated markers, including increased expression of CD39, and were capable of exerting suppressive functions. Corroborating these results in vivo, we observed that neutralizing the tumor pH by systemic administration of sodium bicarbonate (NaBi) decreased Treg abundance. We conclude that acidity augments Treg induction and propose that therapeutic targeting of acidity in the tumor microenvironment (TME) might reduce Treg-mediated immune suppression within tumors.
引用
收藏
页数:15
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