免疫原性
信使核糖核酸
免疫系统
体内
粒径
固体脂质纳米粒
化学
免疫学
病毒学
生物
生物化学
生物技术
基因
物理化学
作者
Kimberly J. Hassett,Jaclyn S. Higgins,Angela Woods,Becca R. Levy,Yan Xia,Chiaowen Joyce Hsiao,Edward P. Acosta,Örn Almarsson,Melissa J. Moore,Luis A. Brito
标识
DOI:10.1016/j.jconrel.2021.05.021
摘要
Lipid nanoparticles (LNP) are effective delivery vehicles for messenger RNA (mRNA) and have shown promise for vaccine applications. Yet there are no published reports detailing how LNP biophysical properties can impact vaccine performance. In our hands, a retrospective analysis of mRNA LNP vaccine in vivo studies revealed a relationship between LNP particle size and immunogenicity in mice using LNPs of various compositions. To further investigate this, we designed a series of studies to systematically change LNP particle size without altering lipid composition and evaluated biophysical properties and immunogenicity of the resulting LNPs. While small diameter LNPs were substantially less immunogenic in mice, all particle sizes tested yielded a robust immune response in non-human primates (NHP).
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