肿瘤微环境
免疫
癌症免疫疗法
免疫疗法
癌症
树突状细胞
癌症研究
医学
启动(农业)
免疫系统
人口
免疫学
生物
内科学
发芽
环境卫生
植物
作者
Ben Wylie,Christophe Macri,Justine D. Mintern,Jason Waithman
出处
期刊:Cancers
[Multidisciplinary Digital Publishing Institute]
日期:2019-04-11
卷期号:11 (4): 521-521
被引量:72
标识
DOI:10.3390/cancers11040521
摘要
Inducing effective anti-tumor immunity has become a major therapeutic strategy against cancer. Dendritic cells (DC) are a heterogenous population of antigen presenting cells that infiltrate tumors. While DC play a critical role in the priming and maintenance of local immunity, their functions are often diminished, or suppressed, by factors encountered in the tumor microenvironment. Furthermore, DC populations with immunosuppressive activities are also recruited to tumors, limiting T cell infiltration and promoting tumor growth. Anti-cancer therapies can impact the function of tumor-associated DC and/or alter their phenotype. Therefore, the design of effective anti-cancer therapies for clinical translation should consider how best to boost tumor-associated DC function to drive anti-tumor immunity. In this review, we discuss the different subsets of tumor-infiltrating DC and their role in anti-tumor immunity. Moreover, we describe strategies to enhance DC function within tumors and harness these cells for effective tumor immunotherapy.
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