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纳米颗粒助力 COVID-19 mRNA 疫苗的成功,微针平台为大流行疫苗应对带来新希望。

The Nanoparticle-Enabled Success of COVID-19 mRNA Vaccines and the Promise of Microneedle Platforms for Pandemic Vaccine Response.

机构信息

Fischell Department of Bioengineering, University of Maryland, College Park, Maryland, USA.

出版信息

DNA Cell Biol. 2022 Jan;41(1):25-29. doi: 10.1089/dna.2021.0538. Epub 2021 Dec 24.

Abstract

The coronavirus disease 2019 (COVID-19) public health crisis has reached critical mass, but interdisciplinary research efforts have provided the global community with the first effective medical intervention to fight the pandemic-COVID-19 vaccines. Two of the vaccines approved for use in the United States and Europe deliver nucleic acid in the form of mRNA, the success of which would not be possible without biomaterials. Lipid nanoparticle (LNP)-based mRNA vaccines, discussed in this perspective, protect nucleic acids from degradation and deliver cargo directly to the intracellular compartment of cells where it is translated into the antigenic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein that triggers protective immune responses. Despite success of LNP-based mRNA vaccines thus far, the pandemic has highlighted the need for emerging technologies that enable rapid development and increased accessibility to vaccination. Microneedle arrays, also discussed in this study, provide features that could lower barriers to vaccine access in resource-poor regions. The ability to exchange antigens within arrays could also facilitate swift vaccine deployment as public health needs evolve (e.g., in response to SARS-CoV-2 variants or entirely new pathogens). Therefore, the COVID-19 pandemic has spotlighted the readiness and value of biomaterials for the prevention and management of disease outbreaks.

摘要

2019 年冠状病毒病(COVID-19)公共卫生危机已达到临界点,但跨学科研究努力为全球社会提供了对抗这一大流行病的首个有效医学干预措施——COVID-19 疫苗。在美国和欧洲批准使用的两种疫苗以信使 RNA(mRNA)的形式递送核酸,如果没有生物材料,这是不可能成功的。本文讨论了基于脂质纳米颗粒(LNP)的 mRNA 疫苗,它可以保护核酸免受降解,并将货物直接递送到细胞的细胞内区室,在那里它被翻译成触发保护性免疫反应的抗原性严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突蛋白。尽管迄今为止基于 LNP 的 mRNA 疫苗取得了成功,但大流行突出表明需要新兴技术来实现疫苗的快速开发和增加可及性。本文还讨论了微针阵列,它提供了一些特性,可以降低资源匮乏地区疫苗接种的障碍。在阵列内交换抗原的能力也可以促进迅速部署疫苗,以应对公共卫生需求的变化(例如,应对 SARS-CoV-2 变体或全新的病原体)。因此,COVID-19 大流行凸显了生物材料在预防和管理疾病爆发方面的准备情况和价值。

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