The Effect of the Tumor Microenvironment and Tumor-Derived Metabolites on Dendritic Cell Function

被引:32
|
作者
Lee, Jun-Ho [1 ,2 ]
Choi, So-Yeon [1 ]
Jung, Nam-Chul [2 ]
Song, Jie-Young [3 ]
Seo, Han Geuk [4 ]
Lee, Hyun Soo [2 ]
Lim, Dae-Seog [1 ]
机构
[1] CHA Univ, Dept Biotechnol, 335 Pangyo Ro, Seongnam 13488, Gyeonggi Do, South Korea
[2] Pharos Vaccine Inc, 545 Dunchon Daero, Seongnam 13215, Gyeonggi Do, South Korea
[3] Korea Inst Radiol & Med Sci, Dept Radiat Canc Sci, 75 Nowon Ro, Seoul 01812, South Korea
[4] Konkuk Univ, Sanghuh Coll Life Sci, Dept Food Sci & Biotechnol Anim Prod, 120 Neungdong Ro, Seoul 05029, South Korea
来源
JOURNAL OF CANCER | 2020年 / 11卷 / 04期
基金
新加坡国家研究基金会;
关键词
dendritic cells; tumor microenvironment; exogenous factor; metabolite; HUMAN SERUM-ALBUMIN; CANCER-IMMUNOTHERAPY; EPITHELIAL-CELLS; T-CELLS; DYSFUNCTION; GENERATION; CD39; CD73; EXPRESSION; VACCINES;
D O I
10.7150/jca.38785
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Dendritic cells (DCs) have a critical effect on the outcome of adaptive immune responses against growing tumors. Recent studies on the metabolism on DCs provide new insights on the functioning of these critical controllers of innate and adaptive immunity. DCs within the tumor microenvironment (TME) often exist in an inactive state, which is thought to limit the adaptive immune response elicited by the growing tumor. Tumor-derived factors in the TME are known to suppress DC activation and result in functional alterations in DC phenotype. We are now beginning to appreciate that many of these factors can also induce changes in immune cell metabolism. In this review, we discuss the functional alternation of DC phenotype by tumor metabolites.
引用
收藏
页码:769 / 775
页数:7
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