CK Exogene, Inc., Seongnam, Gyeonggi do, Republic of Korea.
Methods Mol Biol. 2023;2668:301-311. doi: 10.1007/978-1-0716-3203-1_20.
Extracellular vesicles (EVs) enable cell-to-cell communication and, by delivering antigens, can stimulate the immune response strongly. Approved in use SARS-CoV-2 vaccine, candidates immunize with the viral spike protein delivered via viral vectors, translated by injected mRNAs, or as a pure protein. Here, we outline a novel methodological approach for generating SARS-CoV-2 vaccine using exosome that delivers antigens from the SARS-CoV-2 structural proteins. Engineered EVs can be loaded with viral antigens, thus acting as antigens presenting EVs, eliciting strong and targeted CD8(+) T cell and B cell, offering a unique approach to vaccine development. Engineered EVs thus portray a safe, adaptable, and effective approach for a virus-free vaccine development.
细胞外囊泡 (EVs) 能够实现细胞间通讯,并通过递送抗原强烈刺激免疫反应。已批准使用的 SARS-CoV-2 疫苗,候选疫苗通过病毒载体、注射的 mRNA 或纯蛋白递送来免疫病毒刺突蛋白。在这里,我们概述了一种使用外泌体生成 SARS-CoV-2 疫苗的新方法,该方法可传递来自 SARS-CoV-2 结构蛋白的抗原。工程 EV 可加载病毒抗原,从而充当抗原呈递 EV,引发强烈且靶向的 CD8(+) T 细胞和 B 细胞反应,为疫苗开发提供了一种独特的方法。因此,工程 EV 为无病毒疫苗开发描绘了一种安全、适应性强且有效的方法。