病毒学
抗原
外体
免疫系统
2019年冠状病毒病(COVID-19)
生物
细胞外小泡
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
CD8型
微泡
胞外囊泡
计算生物学
细胞生物学
免疫学
医学
基因
小RNA
遗传学
传染病(医学专业)
病理
疾病
作者
Jae‐Young Kim,Nikita Thapa
标识
DOI:10.1007/978-1-0716-3203-1_20
摘要
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.
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