佐剂
免疫系统
病毒学
病毒
CD8型
信使核糖核酸
接种疫苗
翻译(生物学)
疫苗效力
免疫学
生物
基因
生物化学
作者
Zeliang Lou,Yingying Shi,Xuemeng Guo,Zhaolei Jin,Jiaxin Huang,Yilong Hu,Xü Liu,Jiang Zhu,Rong Kuang,Jian You
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-07-16
被引量:1
标识
DOI:10.1021/acsnano.4c04953
摘要
The efficacy and safety of mRNA vaccines both rely on a fine-tuning of specific humoral and cellular immune responses. Instead of adjustments in vaccine component, we proposed a concept of chronological management of adjuvant effect to modulate the adaptive immune potency and preference inspired by natural virus infection. By simulating type I interferon expression dynamics during viral infection, three vaccine strategies employing distinct exposure sequences of adjuvant and mRNA have been developed, namely Precede, Coincide, and Follow. Follow, the strategy of adjuvant administration following mRNA, effectively suppressed tumor progression, which was attributed to enhanced mRNA translation, augmented p-MHC I expression, and elevated CD8+ T cell response. Meanwhile, Follow exhibited improved biosafety, characterized by reduced incidences of cardiac and liver toxicity, owing to its alteration to the vaccination microenvironment between successive injections. Our strategy highlights the importance of fine-tuning adjuvant effect dynamics in optimizing mRNA vaccines for clinical application.
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