电穿孔
佐剂
免疫疗法
癌症免疫疗法
材料科学
体内
癌症研究
癌症
不可逆电穿孔
免疫原性细胞死亡
CpG寡核苷酸
癌细胞
医学
免疫学
化学
生物
内科学
生物化学
DNA甲基化
生物技术
基因表达
基因
作者
Jun‐Hyeok Han,Yun Young Lee,Ha Eun Shin,Jieun Han,Jeon Min Kang,Chi‐Pin James Wang,Jung‐Hoon Park,Se−Na Kim,Jong-Hwi Yoon,Ho‐Keun Kwon,Dae-Hwan Park,Tae‐Eun Park,Young Bin Choy,Dong‐Hyun Kim,Tae‐Hyung Kim,Junhong Min,Ik-Hwan Kim,Chun Gwon Park,Dong Keun Han,Wooram Park
出处
期刊:Biomaterials
[Elsevier]
日期:2022-08-25
卷期号:289: 121762-121762
被引量:15
标识
DOI:10.1016/j.biomaterials.2022.121762
摘要
Cancer immunotherapy is a next-generation treatment strategy; however, its side effects limit its clinical translation. Here, a novel combination of a multi-functional nano-adjuvant (M-NA) prepared with an iron oxide/gold core and a cationic polymer shell via multilayer synthesis with CpG oligodeoxynucleotide (CpG-ODN) electrostatically complexed on its surface, and irreversible electroporation (IRE) technique was developed for effective image-guided in situ cancer vaccination. The M-NA can be retained long-term in the dense tumoral extracellular matrix after intratumoral injection and internalized by antigen-presenting cells (APCs). The IRE can induce immunogenic cell death. Indeed, in a mouse tumor model, the M-NA showed longer tumor retention time than free CpG-ODN. Compared with other treatments, the combined treatment significantly inhibited tumor growth with 100% survival rate for ∼60 days. The therapy induced the activation of cytotoxic lymphocytes and the maturation of APCs in vivo. This treatment could be effective in image-guided local cancer immunotherapy.
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