细胞毒性T细胞
肿瘤微环境
启动(农业)
CD8型
免疫学
树突状细胞
免疫系统
癌症研究
生物
免疫
癌症
获得性免疫系统
T细胞
体外
发芽
植物
生物化学
遗传学
作者
Morten Hansen,Mads Hald Andersen
标识
DOI:10.1007/s00281-016-0592-y
摘要
Though present in low numbers, dendritic cells (DCs) are recognized as major players in the control of cancer by adaptive immunity. The roles of cytotoxic CD8+ T-cells and Th1 helper CD4+ T-cells are well-documented in murine models of cancer and associated with a profound prognostic impact when infiltrating human tumors, but less information is known about how these T-cells gain access to the tumor or how they are primed to become tumor-specific. Here, we highlight recent findings that demonstrate a vital role of CD103+ DCs, which have been shown to be experts in cross-priming and the induction of anti-tumor immunity. We also focus on two different mediators that impair the function of tumor-associated DCs: prostaglandin E2 and β-catenin. Both of these mediators seem to be important for the exclusion of T-cells in the tumor microenvironment and may represent key pathways to target in optimized treatment regimens against cancer.
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