Safe and Highly Efficient Lipid-Pro-Dexamethasone Nanoparticles for mRNA Delivery and Base Editing

化学 信使核糖核酸 免疫原性 促炎细胞因子 前药 基因传递 遗传增强 纳米颗粒 纳米技术 背景(考古学) 细胞生物学 报告基因 内生 荧光素酶 计算生物学 基因表达 转染 核糖核酸 体内
作者
Yan Zong,Haiping Zhong,Yuqing Wang,Yi Lin,Linxi Zhao,Xiaoyu Wang,Jianan Cai,Haoyang Lin,Yixi Xiao,Tuo Wei,Shutao Guo,Qiang Cheng
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:148 (9): 10225-10240 被引量:1
标识
DOI:10.1021/jacs.6c01708
摘要

The inherent immunogenicity of mRNA lipid nanoparticles (LNPs) poses a major challenge to their application in disease treatment. In this study, we developed a series of innovative dexamethasone (DEX) prodrug ionizable lipids (DPILs) to address the need for safe and effective mRNA delivery, leading to the establishment of the Safe and Highly Efficient Lipid-pro-dexamethasone (SHIELD) LNP platform. The lead formulation, DEX-SPM-CP10 SHIELD LNP, not only markedly decreased the levels of multiple proinflammatory cytokines but also achieved mRNA delivery efficiency comparable to that of the FDA-approved SM-102 LNP. Furthermore, the SHIELD platform demonstrated universality, as incorporating specific ratios of DPILs into various LNPs targeting different organs (such as the liver, lungs, spleen, and pancreas) led to notable reductions in inflammatory responses and enhancements in mRNA expression, highlighting its superiority over strategies that incorporate free DEX. Subsequently, we investigated its application in gene editing therapy by codelivering ABEmax mRNA and sgRNA to edit the EGFP reporter gene and endogenous PCSK9 gene, as well as in protein replacement therapy through multiple injections of mRNA-SHIELD LNPs. All of these results demonstrated excellent delivery efficacy with minimal immunogenicity, fully illustrating the therapeutic potential of this platform. Taken together, the SHIELD platform offers safe and efficient mRNA delivery and has the potential to expand the therapeutic applications of mRNA-based therapies.
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