钙网蛋白
癌症研究
免疫疗法
肺癌
纳米医学
癌症免疫疗法
刘易斯肺癌
癌症
医学
免疫系统
内质网
化学
免疫学
生物
细胞生物学
材料科学
病理
内科学
纳米技术
转移
纳米颗粒
作者
Yuedong Guo,Qunqun Bao,Ping Hu,Jianlin Shi
标识
DOI:10.1038/s41467-023-42972-2
摘要
Pro-tumoral macrophages in lung tumors present a significant challenge in immunotherapy. Here, we introduce a pH-responsive nanomedicine approach for activating anti-tumoral macrophages and dendritic cells. Using a layered double hydroxide nanosheet carrier, we co-deliver a T-type calcium channel inhibitor (TTA-Q6) and a CD47 inhibitor (RRX-001) into lung tumors. In the tumor acidic environment, TTA-Q6 is released, disrupting cancer cell calcium uptake, causing endoplasmic reticulum stress and inducing calreticulin transfer to the cell surface. Surface calreticulin activates macrophages and triggers dendritic cell maturation, promoting effective antigen presentation and therefore activating antitumor T cells. Simultaneously, RRX-001 reduces CD47 protein levels, aiding in preventing immune escape by calreticulin-rich cancer cells. In lung tumor models in male mice, this combined approach shows anti-tumor effects and immunity against tumor re-exposure, highlighting its potential for lung cancer immunotherapy.
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