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用于传染病的核苷修饰mRNA疫苗的生产与评估。

Production and Evaluation of Nucleoside-Modified mRNA Vaccines for Infectious Diseases.

作者信息

Vadovics Máté, Muramatsu Hiromi, Sárközy András, Pardi Norbert

机构信息

Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Methods Mol Biol. 2024;2786:167-181. doi: 10.1007/978-1-0716-3770-8_7.

Abstract

Lipid nanoparticle (LNP)-encapsulated nucleoside-modified mRNA vaccines have demonstrated potency in multiple preclinical models against various pathogens and have recently received considerable attention due to the success of the two safe and effective COVID-19 mRNA vaccines developed by Moderna and Pfizer-BioNTech. The use of nucleoside modification in mRNA vaccines seems to be critical to achieve a sufficient level of safety and immunogenicity in humans, as illustrated by the results of clinical trials using either nucleoside-modified or unmodified mRNA-based vaccine platforms. It is well documented that the incorporation of modified nucleosides in the mRNA and stringent mRNA purification after in vitro transcription render it less inflammatory and highly translatable; these two features are likely key for mRNA vaccine safety and potency. Formulation of the mRNA into LNPs is important because LNPs protect mRNA from rapid degradation, enabling efficient delivery and high levels of protein production for extended periods of time. Additionally, recent studies have provided evidence that certain LNPs with ionizable cationic lipids (iLNPs) possess adjuvant activity that fosters the induction of strong humoral and cellular immune responses by mRNA-iLNP vaccines.In this chapter we describe the production of iLNP-encapsulated, nucleoside-modified, and purified mRNA and the evaluation of antigen-specific T cell and antibody responses elicited by this vaccine form.

摘要

脂质纳米颗粒(LNP)包裹的核苷修饰mRNA疫苗已在多种针对不同病原体的临床前模型中显示出效力,并且由于Moderna和辉瑞- BioNTech研发的两款安全有效的新冠mRNA疫苗取得成功,最近受到了广泛关注。在mRNA疫苗中使用核苷修饰对于在人体中实现足够的安全性和免疫原性似乎至关重要,使用核苷修饰或未修饰的mRNA疫苗平台进行的临床试验结果就说明了这一点。有充分的文献记载,在mRNA中掺入修饰核苷以及体外转录后进行严格的mRNA纯化,使其炎症性降低且具有高度可翻译性;这两个特性可能是mRNA疫苗安全性和效力的关键。将mRNA制成LNP很重要,因为LNP可保护mRNA不被快速降解,从而实现高效递送并在较长时间内高水平表达蛋白质。此外,最近的研究提供了证据,表明某些含有可电离阳离子脂质的LNP(iLNP)具有佐剂活性,可促进mRNA-iLNP疫苗诱导强烈的体液免疫和细胞免疫反应。在本章中,我们描述了iLNP包裹、核苷修饰和纯化的mRNA的生产,以及这种疫苗形式引发的抗原特异性T细胞和抗体反应的评估。

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