Immunity beyond cancer cells: perspective from tumor tissue

被引:36
作者
Gao, Shengyu [1 ,2 ]
Hsu, Ting-Wei [1 ,3 ,4 ]
Li, Ming O. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Immunol Program, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Louis V Gerstner Jr Grad Sch Biomed Sci, New York, NY 10065 USA
[3] Cornell Univ, Grad Program Biochem & Struct Biol, Cell & Dev Biol, Weill Cornell Grad Sch Med Sci, New York, NY 10065 USA
[4] Cornell Univ, Mol Biol, Weill Cornell Grad Sch Med Sci, New York, NY 10065 USA
来源
TRENDS IN CANCER | 2021年 / 7卷 / 11期
关键词
T-CELL; DEPENDENT MECHANISM; ACQUIRED-RESISTANCE; PROSTATE-CANCER; TH2; CELLS; IL-17; PROMOTES; MICROENVIRONMENT; DIFFERENTIATION; IMMUNOTHERAPY;
D O I
10.1016/j.trecan.2021.06.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Investigation of cancer as a cell-level disease has led to the development of cancer cell-directed therapies including cytotoxic T lymphocyte (CTL)-based immunotherapy; yet, many patients are refractory to these modalities of cancer treatment and acquired resistance frequently occurs. Of note, cancer environment controls the manifestation of cancerous cell phenotype. Helper T (Th) cells orchestrate immune defense responses targeting cancer cells as well as the tumor microenvironment. Recent studies have shown that in addition to interferon (IFN)-gamma-producing Th1 cells, interleukin (IL)-4-producing Th2 cells function as potent anticancer effectors in part by promoting tumor stroma reconfiguration and tumor tissue repair. Such Th cell-mediated tissue-level immunity may be harnessed for novel modalities of cancer environment immunotherapy.
引用
收藏
页码:1010 / 1019
页数:10
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