Promising Targets for Cancer Immunotherapy: TLRs, RLRs, and STING-Mediated Innate Immune Pathways

被引:129
|
作者
Li, Kai [1 ]
Qu, Shuai [1 ]
Chen, Xi [1 ]
Wu, Qiong [1 ]
Shi, Ming [1 ,2 ]
机构
[1] Harbin Inst Technol, Sch Life Sci & Technol, Harbin 150080, Peoples R China
[2] Harbin Inst Technol, Room 310,Bldg 2E,Sci Pk,2 Yikuang St, Harbin 150080, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
cancer immunotherapy; innate immunity; Toll-like Receptors; RIG-I-like Receptors; Stimulator of Interferon Genes; TOLL-LIKE RECEPTOR; CYTOSOLIC DNA SENSOR; RIG-I ACTIVATION; CYCLIC GMP-AMP; CELL-DEATH; DENDRITIC CELLS; ANTITUMOR IMMUNITY; GENE INDUCTION; AGONIST; T-CELLS;
D O I
10.3390/ijms18020404
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Malignant cancers employ diverse and intricate immune evasion strategies, which lead to inadequately effective responses of many clinical cancer therapies. However, emerging data suggest that activation of the tolerant innate immune system in cancer patients is able, at least partially, to counteract tumor-induced immunosuppression, which indicates triggering of the innate immune response as a novel immunotherapeutic strategy may result in improved therapeutic outcomes for cancer patients. The promising innate immune targets include Toll-like Receptors (TLRs), RIG-I-like Receptors (RLRs), and Stimulator of Interferon Genes (STING). This review discusses the antitumor properties of TLRs, RLRs, and STING-mediated innate immune pathways, as well as the promising innate immune targets for potential application in cancer immunotherapy.
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收藏
页数:19
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