Opposing Roles of Type I Interferons in Cancer Immunity

被引:114
|
作者
Boukhaled, Giselle M. [1 ,2 ]
Harding, Shane [1 ,2 ,3 ,4 ]
Brooks, David G. [1 ,2 ]
机构
[1] Univ Hlth Network Toronto, Princess Margaret Canc Ctr, Toronto, ON M5G 2M9, Canada
[2] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Med Biophys, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Dept Radiat Oncol, Toronto, ON M5S 1A8, Canada
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
type I interferon; IFN-I; cancer immunology; hallmarks of cancer; immunotherapy; IFN-stimulated gene; ISG; CD8; T-CELLS; ENDOTHELIAL GROWTH-FACTOR; EPITHELIAL-MESENCHYMAL TRANSITION; DENDRITIC CELLS; CHECKPOINT BLOCKADE; PD-1; BLOCKADE; STAGE-III; INDOLEAMINE 2,3-DIOXYGENASE; MAINTENANCE TREATMENT; COLORECTAL-CANCER;
D O I
10.1146/annurev-pathol-031920-093932
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The immune system is tasked with identifying malignant cells to eliminate or prevent cancer spread. This involves a complex orchestration of many immune cell types that together recognize different aspects of tumor transformation and growth. In response, tumors have developed mechanisms to circumvent immune attack. Type I interferons (IFN-Is) are a class of proinflammatory cytokines produced in response to viruses and other environmental stressors. IFN-Is are also emerging as essential drivers of antitumor immunity, potently stimulating the ability of immune cells to eliminate tumor cells. However, a more complicated role for IFN-Is has arisen, as prolonged stimulation can promote feedback inhibitory mechanisms that contribute to immune exhaustion and other deleterious effects that directly or indirectly permit cancer cells to escape immune clearance. We review the fundamental and opposing functions of IFN-Is that modulate tumor growth and impact immune function and ultimately how these functions can be harnessed for the design of new cancer therapies.
引用
收藏
页码:167 / 198
页数:32
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