CpG寡核苷酸
免疫疗法
癌症研究
免疫系统
化学免疫疗法
癌症免疫疗法
CpG站点
免疫原性细胞死亡
肿瘤微环境
抗原呈递
抗原
免疫学
细胞毒性T细胞
树突状细胞
生物
T细胞
体外
DNA甲基化
基因
基因表达
生物化学
作者
Haihui Wang,Xiaohui Zhu,Han Xiao,Yongfei Liu,Zhangcheng Fu,Yihang Ding,Chunsen Li,Chunhua Lü,Xian-kun Tu
标识
DOI:10.1016/j.matdes.2022.111159
摘要
Induction of antigen-specific immune response by maturing dendritic cells (DCs) is a promising strategy for anti-tumor immunotherapy. However, the immunosuppressive tumor microenvironment (TME) and the ineffective tumor-associated antigen (TAAs) presentation of DCs have hindered the efficacy of immunotherapy. Herein, we developed an immunostimulatory nanosphere by direct self-assembly of cyanine5 labeled CPG oligodeoxynucleotide and doxorubicin (Cy5-CPG/DOX). The introduction of Cy5 into CPG could increase the interaction of Cy5-CPG and DOX, accelerating the formation of Cy5-CPG/DOX nanosphere. In vivo, DOX can effectively downregulate the level of regulatory T cells to reverse and abrogate immunosuppressive. Meanwhile, DOX induce immunogenic cell death to produce TAAs, which combined with Cy5-CPG promote the maturation of DCs, improving the TAAs presentation ability of DCs. Thus, the Cy5-CPG/DOX could awaken the innate immune system, sensitizing tumors to immune checkpoint inhibitors mediated by the programmed death-ligand 1 (PD-L1) antibody. In this way, the Cy5-CPG/DOX combined with PD-L1 can decrease the exhaustion of cytotoxic T lymphocytes, eliciting a durable systemic anti-tumor immunity to eradicate cancer. Our work establishes a stable approach for constructing immunostimulatory nanodrug, promoting the development of progressive therapeutic systems.
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