肿瘤微环境
免疫疗法
免疫系统
癌症免疫疗法
树突状细胞
纳米载体
巨噬细胞极化
获得性免疫系统
癌症研究
材料科学
免疫学
T细胞
癌症疫苗
抗原
巨噬细胞
医学
生物
纳米技术
体外
纳米颗粒
生物化学
作者
Feng Liu,Junlin Sun,Wenqian Yu,Qunying Jiang,Min Pan,Zhen Xu,Fengye Mo,Xiaoqing Liu
出处
期刊:Biomaterials
[Elsevier]
日期:2020-02-29
卷期号:242: 119928-119928
被引量:46
标识
DOI:10.1016/j.biomaterials.2020.119928
摘要
Dendritic cell (DC) vaccines hold great potential in cancer immunotherapy, but the suboptimal design of DC vaccines and the immunosuppressive tumor microenvironment largely impair their anti-tumor efficacy. Here, quantum dot (QD) pulsed-DC vaccines integrating with tumor-associated macrophage polarization are developed for amplified anti-tumor immunity. Semiconductor QDs are engineered with diverse functions to act as fluorescence nanoprobes, immunomodulatory adjuvants, and nanocarriers to load tumor antigens and Toll-like receptor 9 agonists. The QD-pulsed DC vaccines enable spatiotemporal tracking of lymphatic drainage and efficacy evaluation of DC immunotherapy, and trigger potent immunoactivation. Specifically, designer DC vaccine plus macrophage polarization elicits potent immune response to stimulate innate and adaptive antitumor immunity and ameliorate the immunosuppressive tumor microenvironment. As a new combination therapy, this strategy greatly boosts antigen-specific T-cell immunity and thus strongly inhibits local tumor growth and tumor metastasis in vivo. This study may provide an applicable treatment for cancer immunotherapy.
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