启动(农业)
T细胞
抗原
CD8型
交叉展示
树突状细胞
抗原呈递
免疫学
抗原提呈细胞
C-C趋化因子受体7型
细胞毒性T细胞
细胞生物学
癌症研究
生物
免疫系统
趋化因子
趋化因子受体
体外
发芽
植物
生物化学
作者
Edward W. Roberts,Miranda L. Broz,Mikhail Binnewies,Mark B. Headley,Amanda E. Nelson,Denise M. Wolf,Tsuneyasu Kaisho,Dusan Bogunovic,Nina Bhardwaj,Matthew F. Krummel
出处
期刊:Cancer Cell
[Elsevier]
日期:2016-07-16
卷期号:30 (2): 324-336
被引量:947
标识
DOI:10.1016/j.ccell.2016.06.003
摘要
Intratumoral dendritic cells (DC) bearing CD103 in mice or CD141 in humans drive intratumoral CD8+ T cell activation. Using multiple strategies, we identified a critical role for these DC in trafficking tumor antigen to lymph nodes (LN), resulting in both direct CD8+ T cell stimulation and antigen hand-off to resident myeloid cells. These effects all required CCR7. Live imaging demonstrated direct presentation to T cells in LN, and CCR7 loss specifically in these cells resulted in defective LN T cell priming and increased tumor outgrowth. CCR7 expression levels in human tumors correlate with signatures of CD141+ DC, intratumoral T cells, and better clinical outcomes. This work identifies an ongoing pathway to T cell priming, which should be harnessed for tumor therapies.
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