Gardner Alycia, Ruffell Brian
Department of Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA; Cancer Biology PhD Program, University of South Florida, Tampa, FL, USA.
Department of Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA; Breast Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Trends Immunol. 2016 Dec;37(12):855-865. doi: 10.1016/j.it.2016.09.006. Epub 2016 Oct 25.
Dendritic cells (DCs) are central regulators of the adaptive immune response, and as such are necessary for T-cell-mediated cancer immunity. In particular, antitumoral responses depend on a specialized subset of conventional DCs that transport tumor antigens to draining lymph nodes and cross-present antigen to activate cytotoxic T lymphocytes. DC maturation is necessary to provide costimulatory signals to T cells, but while DC maturation occurs within tumors, it is often insufficient to induce potent immunity, particularly in light of suppressive mechanisms within tumors. Bypassing suppressive pathways or directly activating DCs can unleash a T-cell response, and although clinical efficacy has proven elusive, therapeutic targeting of DCs continues to hold translational potential in combinatorial approaches.
树突状细胞(DCs)是适应性免疫反应的核心调节因子,因此对于T细胞介导的癌症免疫至关重要。特别是,抗肿瘤反应依赖于一类特殊的传统DCs,它们将肿瘤抗原转运至引流淋巴结,并交叉呈递抗原以激活细胞毒性T淋巴细胞。DC成熟对于向T细胞提供共刺激信号是必要的,然而,尽管DC成熟在肿瘤内发生,但通常不足以诱导强大的免疫反应,尤其是考虑到肿瘤内的抑制机制。绕过抑制途径或直接激活DCs可引发T细胞反应,尽管临床疗效难以捉摸,但DC的治疗性靶向在联合治疗方法中仍具有转化潜力。