Sæbøe-Larssen Stein, Sioud Mouldy
Section for Cellular Therapy, Department of Oncology, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
Division of Cancer Medicine, Department of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
Methods Mol Biol. 2025;2965:235-244. doi: 10.1007/978-1-0716-4742-4_10.
Harnessing the potential of mRNAs to express proteins of interest has emerged as a powerful tool in biotechnology and medicine, particularly in the development of vaccines. Such mRNAs can be in-vitro transcribed (IVT) in a controlled laboratory environment using a DNA template that encodes the protein of interest. Key components required include the DNA template, T7 RNA polymerase, ribonucleoside triphosphates, and necessary cofactors. The resulting mRNA is then purified and can be loaded directly into target cells ex vivo or formulated into lipid nanoparticles for in vivo delivery as, e.g. a vaccine. IVT-produced mRNA vaccines offer rapid development, high efficacy, and a versatile platform, as demonstrated by the success of COVID-19 vaccines. In this chapter, we describe the production and purification of unmodified IVT mRNA for ex vivo generation of dendritic cell (DC) mRNA vaccines or T cells engineered with chimeric antigen receptors.
利用信使核糖核酸(mRNA)表达感兴趣蛋白质的潜力已成为生物技术和医学领域的一项强大工具,尤其是在疫苗开发方面。此类mRNA可在受控的实验室环境中使用编码感兴趣蛋白质的DNA模板进行体外转录(IVT)。所需的关键组件包括DNA模板、T7 RNA聚合酶、核糖核苷三磷酸和必要的辅助因子。然后对产生的mRNA进行纯化,它可以直接在体外加载到靶细胞中,或者配制成脂质纳米颗粒用于体内递送,例如作为疫苗。正如新冠病毒疫苗的成功所证明的那样,IVT生产的mRNA疫苗具有开发迅速、效力高和平台通用性强的特点。在本章中,我们描述了未修饰的IVT mRNA的生产和纯化方法,用于体外生成树突状细胞(DC)mRNA疫苗或用嵌合抗原受体工程改造的T细胞。