Innate immune mediators in cancer: between defense and resistance

被引:150
作者
Berraondo, Pedro [1 ,2 ]
Minute, Luna [1 ,2 ]
Ajona, Daniel [1 ,3 ,4 ]
Corrales, Leticia [5 ]
Melero, Ignacio [1 ,2 ]
Pio, Ruben [1 ,3 ,4 ]
机构
[1] Navarra Inst Hlth Res IDISNA, Pamplona, Spain
[2] Ctr Appl Med Res CIMA, Program Immunol & Immunotherapy, Pamplona, Spain
[3] CIMA, Program Solid Tumors & Biomarkers, Pamplona, Spain
[4] Univ Navarra, Sch Sci, Dept Biochem & Genet, Pamplona, Spain
[5] Aduro Biotech, Berkeley, CA USA
基金
欧盟地平线“2020”;
关键词
B cells; complement system; dendritic cells; macrophages; myeloid-derived suppressor cells; natural killer cells; STING; NATURAL-KILLER-CELLS; COMPLEMENT FACTOR-H; PHASE-I TRIAL; ACTIVATION PRODUCT C4D; CYCLIC GMP-AMP; T-CELL; DENDRITIC CELLS; LUNG-CANCER; HLA-E; INTRATUMORAL INJECTION;
D O I
10.1111/imr.12464
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Chronic inflammation in the tumor microenvironment and evasion of the antitumor effector immune response are two of the emerging hallmarks required for oncogenesis and cancer progression. The innate immune system not only plays a critical role in perpetuating these tumor-promoting hallmarks but also in developing antitumor adaptive immune responses. Thus, understanding the dual role of the innate system in cancer immunology is required for the design of combined immunotherapy strategies able to tackle established tumors. Here, we review recent advances in the understanding of the role of cell populations and soluble components of the innate immune system in cancer, with a focus on complement, the adapter molecule Stimulator of Interferon Genes, natural killer cells, myeloid cells, and B cells.
引用
收藏
页码:290 / 306
页数:17
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