免疫原性细胞死亡
免疫系统
癌症研究
全身给药
获得性免疫系统
先天免疫系统
免疫疗法
细胞凋亡
细胞毒性T细胞
免疫
生物
CD8型
免疫学
体内
体外
生物化学
生物技术
作者
Jingyi Wang,Beibei Guo,Zhiwei Sun,Songsong Zhao,Li Cao,Zhiyuan Zhong,Fenghua Meng
标识
DOI:10.1002/adhm.202400784
摘要
Immunotherapy has emerged as a powerful weapon against lung cancer, yet only a fraction of patients respond to the treatment. Poly(I:C) (PIC) effectively triggers both innate and adaptive immunity. It can also induce immunogenic cell death (ICD) in tumor cells. However, its efficacy is hindered by its instability in vivo and limited cellular uptake. To address this, PIC is encapsulated in cRGD-functionalized polymersomes (t-PPIC), which significantly increases its stability and uptake, thus activating dendritic cells (DCs) and inducing apoptosis of lung tumor cells in vitro. In a murine LLC lung tumor model, systemic administration of t-PPIC effectively suppresses tumor growth and leads to survival benefits, with 40% of the mice becoming tumor-free. Notably, t-PPIC provokes stronger apoptosis and ICD in tumor tissue and elicits a more potent stimulation of DCs, recruitment of natural killer (NK) cells, and activation of CD8
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