体内
信使核糖核酸
原位
生物
免疫系统
胶体金
分子生物学
离体
体外
黑色素瘤
计算生物学
纳米颗粒
纳米技术
限制
纳米医学
免疫调节
化学
细胞生物学
链霉亲和素
材料科学
作者
A. Cris Hamilton,Ajay S. Thatte,Jiayi Xu,Zhangyi Luo,Hannah C. Safford,Kelsey L. Swingle,Jenna Muscat‐Rivera,Michael Kegel,Xuexiang Han,Ryann A Joseph,Amanda M. Murray,Hannah C. Geisler,Ricardo Whitaker,Lulu Xue,Roman Spektor,Jilian R. Melamed,Drew Weissman,Michael J. Mitchell
标识
DOI:10.1002/adma.202514370
摘要
Interest continues to grow in the use of mRNA vaccines and therapeutics. While effective for immunization against infectious diseases, lipid nanoparticle (LNP) formulations used for other mRNA delivery applications suffer from off-target accumulation, poor immune transfection, and reactogenicity, limiting their application to immunoengineering. Development of new mRNA LNPs is severely bottlenecked by the LNP discovery process, which is historically low-throughput due to reliance on low-plex measurements. Here, we develop a high-throughput in vivo mRNA LNP screening platform based on barcoded mRNA (b-mRNA). Using this b-mRNA screening platform to simultaneously evaluate 122 LNPs, we identify novel LNP formulations capable of potent hepatic and extrahepatic transfection. We evaluate a lead LNP candidate for in situ immune modulation in a syngeneic mouse model of melanoma and demonstrate a significant reduction in tumor burden and extended survival compared to mice treated with a gold standard mRNA LNP formulation. We employ novel biochemical characterization techniques to analyze nanoparticle protein corona formation with single-particle resolution and gain insight into the influence of protein adsorption on hepatic and splenic transfection. Together, our results demonstrate the value of advanced LNP screening and characterization techniques for the development of next-generation mRNA LNPs for immunoengineering.
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