聚乙烯亚胺
抗原
卵清蛋白
材料科学
先天免疫系统
电化学疗法
免疫系统
癌症研究
免疫学
医学
生物
电穿孔
基因
生物化学
转染
作者
Jiayu Zhao,Yudi Xu,Sheng Ma,Yibo Wang,Zichao Huang,Haoyuan Qu,Haochen Yao,Yu Zhang,Guanglu Wu,Leaf Huang,Wantong Song,Zhaohui Tang,Xuesi Chen
标识
DOI:10.1002/adma.202109254
摘要
In recent years, significant evolutions have been made in applying nanotechnologies for prophylactic and therapeutic cancer vaccine design. However, the clinical translation of nanovaccines is still limited owing to their complicated compositions and difficulties in the spatiotemporal coordination of antigen-presenting cell activation and antigen cross-presentation. Herein, a minimalist binary nanovaccine (BiVax) is designed that integrates innate stimulating activity into the carrier to elicit robust antitumor immunity. The authors started by making a series of azole molecules end-capped polyethylenimine (PEI-M), and were surprised to find that over 60% of the PEI-M polymers have innate stimulating activity via activation of the stimulator of interferon genes pathway. PEI-4BImi, a PEI-M obtained from a series of polymers, elicits robust antitumor immune responses when used as a subcutaneously injected nanovaccine by simply mixing with ovalbumin antigens, and this BiVax system performs much better than the traditional ternary vaccine system, as well as, commercialized aluminum-containing adjuvants. This system also enables the fast preparation of personalized BiVax by compositing PEI-4BImi with autologous tumor cell membrane protein antigens, and a 60% postoperative cure rate is observed when combined with immune checkpoint inhibitors.
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