Exosomes-based particles as inhalable COVID-19 vaccines

Lu Fan , Li Wang , Xiaoju Wang , Hongbo Zhang
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引用次数: 2

Abstract

Coronavirus disease 2019 (COVID-19), a severely spreading pandemic, has dramatically brought physiological and economical burdens to people. Although the injectable vaccines have some achievements for coronavirus defense, they still generate accompanied pain, untoward reaction and cannot take part in mucosal immunity. Inhalable vaccines, as a safe, facile and efficient strategy, have been presented to protect body from virus by inducing robust mucosal immunity. Here, we give a perspective of an inhalable COVID-19 vaccine composed of lung-derived exosomes (a type of virus-like particle) conjugated with viral receptor-binding domain. The lung-derived exosomes act as carriers, such inhalable particles successfully reach at lung and reveal wider distribution and longer retention on respiratory mucosa. In addition, such vaccines induce the high production of specific antibodies and T cells in lung, significantly protecting host against coronavirus invasion. It is conceived that inhalable virus-like particles with long-term stability wound open a new avenue for vaccines delivery and further achieve vaccine popularization to against with COVID-19 pandemic.

基于外泌体的颗粒作为可吸入性COVID-19疫苗
2019冠状病毒病(新冠肺炎)是一种严重传播的流行病,给人们带来了巨大的生理和经济负担。尽管注射疫苗在冠状病毒防御方面取得了一些成就,但它们仍然会产生伴随的疼痛、不良反应,并且不能参与粘膜免疫。可吸入疫苗作为一种安全、简便、有效的策略,已被提出通过诱导强大的粘膜免疫来保护身体免受病毒感染。在此,我们对可吸入的新冠肺炎疫苗进行了展望,该疫苗由肺来源的外泌体(一种病毒样颗粒)与病毒受体结合结构域结合而成。肺来源的外泌体作为载体,这种可吸入颗粒成功到达肺部,并在呼吸道粘膜上显示出更宽的分布和更长的滞留时间。此外,此类疫苗可诱导肺部产生大量特异性抗体和T细胞,显著保护宿主免受冠状病毒入侵。认为具有长期稳定性的可吸入病毒样颗粒物将为疫苗的提供开辟新的途径,并进一步实现针对新冠肺炎大流行的疫苗普及。
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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CiteScore
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