肿瘤微环境
免疫系统
细胞毒性T细胞
树突状细胞
生物
免疫疗法
癌症
癌症研究
趋化因子
癌细胞
免疫学
癌症免疫疗法
体外
遗传学
生物化学
作者
Jan P. Böttcher,Caetano Reis e Sousa
标识
DOI:10.1016/j.trecan.2018.09.001
摘要
Dendritic cells (DCs) are key orchestrators of immune responses. A specific DC subset, conventional type 1 DCs (cDC1s), has been recently associated with human cancer patient survival and, in preclinical models, is critical for the spontaneous rejection of immunogenic cancers and for the success of T cell-based immunotherapies. The unique role of cDC1 reflects the ability to initiate de novo T cell responses after migrating to tumor-draining lymph nodes, as well as to attract T cells, secrete cytokines, and present tumor antigens within the tumor microenvironment, enhancing local cytotoxic T cell function. Strategies aimed at increasing cDC1 abundance in tumors and enhancing their functionality provide attractive new avenues to boost anti-tumor immunity and overcome resistance to cancer immunotherapies.
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