免疫系统
获得性免疫系统
生物
CD8型
癌症研究
抗原
抗原呈递
癌变
免疫
免疫学
T细胞
癌症
遗传学
作者
Lili Zhou,Shouxin Zhang,Yongqiang Wang,Meirong Zhang,Wenhuan Sun,Tong Dai,Aijun Wang,Xiaojin Wu,Suping Zhang,Shuai Wang,Fangfang Zhou
标识
DOI:10.1002/adbi.201900237
摘要
Abstract Type I interferons (IFN‐Is) are a family of cytokines that exert direct antiviral effects and regulate innate and adaptive immune responses through direct and indirect mechanisms. It is generally believed that IFN‐Is repress tumor development via restricting tumor proliferation and inducing antitumor immune responses. However, recent emerging evidence suggests that IFN‐Is play a dual role in antitumor immunity. That is, in the early stage of tumorigenesis, IFN‐Is promote the antitumor immune response by enhancing antigen presentation in antigen‐presenting cells and activating CD8 + T cells. However, in the late stage of tumor progression, persistent expression of IFN‐Is induces the expression of immunosuppressive factors (PD‐L1, IDO, and IL‐10) on the surface of dendritic cells and other bone marrow cells and inhibits their antitumor immunity. This review outlines these dual functions of IFN‐Is in antitumor immunity and elucidates the involved mechanisms, as well as their applications in tumor therapy.
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