Synthesis of Dendritic Cell-Targeted Polymeric Nanoparticles for Selective Delivery of mRNA Vaccines to Elicit Enhanced Immune Responses

Chi-Huey Wong
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Abstract

ABSTRACT: Recent development of SARS-CoV-2 spike mRNA vaccines to control the pandemic is a breakthrough in the field of vaccine development. mRNA vaccines are generally formulated with lipid nanoparticles (LNPs) which are composed of several lipids with specific ratios; however, they generally lack selective delivery. To develop a simpler method selective delivery of mRNA, we reported here the synthesis of biodegradable copolymers decorated with guanidine and zwitterionic groups and an aryl-trimannoside ligand as polymeric nanoparticles (PNPs) for encapsulation and selective delivery of an mRNA to dendritic cells (DCs). A representative DC-targeted SARS-CoV-2 spike mRNA-PNP vaccine was shown to elicit a stronger protective immune response in mice as compared to the mRNA-LNP and mRNA-PNP vaccines without the selective delivery design. It is anticipated that this technology will be generally applicable to development of DC-targeted mRNA vaccines with enhanced immune response.
树突状细胞靶向聚合纳米颗粒的合成用于mRNA疫苗的选择性递送以引发增强的免疫反应
摘要:近年来,SARS-CoV-2刺突mRNA疫苗的研制是疫苗开发领域的重大突破。mRNA疫苗通常用脂质纳米颗粒(LNPs)配制,LNPs由几种特定比例的脂质组成;然而,它们通常缺乏选择性交付。为了开发一种更简单的选择性递送mRNA的方法,我们在这里报道了用胍和两性离子基团修饰的可生物降解共聚物和芳基三甲苷配体作为聚合物纳米颗粒(PNPs)的合成,用于包裹和选择性递送mRNA到树突状细胞(dc)。与没有选择性递送设计的mRNA-LNP和mRNA-PNP疫苗相比,具有代表性的dc靶向SARS-CoV-2刺突mRNA-PNP疫苗在小鼠中引发了更强的保护性免疫反应。预计该技术将普遍适用于dc靶向mRNA疫苗的开发,增强免疫应答。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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