Targeting Metabolic Pathways of Myeloid Cells Improves Cancer Immunotherapy

被引:19
|
作者
Li, Jianying [1 ,2 ]
Bolyard, Chelsea [1 ,2 ]
Xin, Gang [1 ,2 ,3 ]
Li, Zihai [1 ,2 ,4 ]
机构
[1] Ohio State Univ, Comprehens Canc Center, Arthur G James Canc Hosp, Pelotonia Inst Immuno Oncol, Columbus, OH 43210 USA
[2] Ohio State Univ, Richard J Solove Res Inst, Columbus, OH 43210 USA
[3] Ohio State Univ, Coll Med, Dept Microbial Infect & Immun, Columbus, OH USA
[4] Ohio State Univ, Dept Med Oncol, Coll Med, Columbus, OH USA
基金
美国国家卫生研究院;
关键词
myeloid cells; immunometabolism; immunotherapy; tumor-associated macrophages; tumor-infiltrating myeloid cells; tumor-associated dendritic cells; myeloid-derived suppressor cells; tumor-associated neutrophils; TUMOR-ASSOCIATED MACROPHAGES; SUPPRESSOR-CELLS; NITRIC-OXIDE; MURINE MACROPHAGES; IMMUNE SUPPRESSION; IDO EXPRESSION; L-ARGININE; ACTIVATION; MICROENVIRONMENT; GROWTH;
D O I
10.3389/fcell.2021.747863
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tumor-infiltrating myeloid cells are a prominent pro-tumorigenic immune cell population that limit host anti-tumor immunity and present a significant obstacle for many cancer immunotherapies. Targeting the mechanisms regulating myeloid cell function within the tumor microenvironment may overcome immunotherapy resistance in some cancers. Recent discoveries in the emerging field of immunometabolism reveal that the metabolic profiles of intratumoral myeloid cells are rewired to adapt to the nutrition-limited tumor microenvironment, and this shapes their pro-tumor phenotypes. Interestingly, metabolic modulation can shift these myeloid cells toward the immune-stimulating anti-tumor phenotype. In this review, we will highlight the roles of specific metabolic pathways in the activation and function of myeloid cells, and discuss the therapeutic value of metabolically reprogramming myeloid cells to augment and improve outcomes with cancer immunotherapy.
引用
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页数:13
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