Type I interferon-mediated tumor immunity and its role in immunotherapy

被引:196
作者
Yu, Renren [1 ,2 ]
Zhu, Bo [1 ,3 ]
Chen, Degao [1 ]
机构
[1] Third Mil Med Univ, Inst Canc, Xinqiao Hosp, Chongqing 400037, Peoples R China
[2] Wenzhou Med Univ, Affiliated Hosp 1, Dept Oncol, Wenzhou 325000, Peoples R China
[3] Third Mil Med Univ, Xinqiao Hosp, Chongqing Key Lab Immunotherapy, Chongqing 400037, Peoples R China
基金
中国国家自然科学基金;
关键词
IFN-alpha; IFN-beta; Tumor immunity; cGAS; STING; Radiation therapy; Oncolytic virotherapy; REGULATORY T-CELLS; CYCLIC GMP-AMP; ANTITUMOR IMMUNITY; PD-1; BLOCKADE; STING PATHWAY; IFN; CANCER; DNA; ALPHA; RESPONSES;
D O I
10.1007/s00018-022-04219-z
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
Immune checkpoint blockade (ICB) therapies have achieved remarkable clinical responses in patients with many different types of cancer; however, most patients who receive ICB monotherapy fail to achieve long-term responses, and some tumors become immunotherapy-resistant and even hyperprogressive. Type I interferons (IFNs) have been demonstrated to inhibit tumor growth directly and indirectly by acting upon tumor and immune cells, respectively. Furthermore, accumulating evidence indicates that endo- and exogenously enhancing type I IFNs have a synergistic effect on anti-tumor immunity. Therefore, clinical trials studying new treatment strategies that combine type I IFN inducers with ICB are currently in progress. Here, we review the cellular sources of type I IFNs and their roles in the immune regulation of the tumor microenvironment. In addition, we highlight immunotherapies based on type I IFNs and combination therapy between type I IFN inducers and ICBs.
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页数:24
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