TLR7型
树突状细胞
肿瘤微环境
免疫疗法
癌症研究
免疫系统
免疫学
医学
肿瘤细胞
先天免疫系统
Toll样受体
作者
Hongyu Chu,Yuezhan Shan,Zongyu Liu,Mengmeng Sun,Weidong Zhao,Xiao Xie,Kun Wang,Chenguang Yang,Xuedong Fang,Na Shen,Zhaohui Tang
标识
DOI:10.1002/adma.202412974
摘要
Intratumoral dendritic cells (DCs) are pivotal in tumor treatment due to their immature and pro-tumoral state induced by the tumor microenvironment. Clinically, these immature DCs correlate with disease progression and recurrence, adversely affecting prognosis. Activation of DCs by the TLR7/8 agonist imidazoquinoline (IMDQ) has yielded promising results, but they are limited by systemic inflammation risks, and high programmed death ligand 1 (PDL1) expression on DCs impedes CD8+ T cell activity. Thus, the study introduces an antibody-polymeric IMDQ complex (αPDL1-PLG-IMDQ) with an ultrahigh drug-to-antibody ratio, where αPDL1 is conjugated to Fc-binding peptides on polymeric IMDQ. This complex targets high PDL1-expressing intratumoral DCs with high probability, inducing PDL1-mediated endocytosis to deliver IMDQ to TLR7/8 within endosomes, effectively activating DCs (CD11c+MHC II+: 2.33% versus 1.09%, CD11c+CD86+: 2.49% versus 1.00% on tumors compared to phosphate-buffered saline treatment) and priming T cells. It also blocks PDL1/PD1 interactions, enhancing tumor-specific T-cell activation and memory. Notably, αPDL1-PLG-IMDQ achieved a 97% tumor inhibition rate, prevented tumor regrowth in rechallenge experiments, and reduced lung metastases of tumors by 83%. These findings underscore its potential for intratumoral DC-targeted immunotherapy and novel systemic IMDQ and checkpoint inhibitor combinations.
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