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用于重编程人树突状细胞和T细胞的未修饰mRNA的大规模生产

Large-Scale Production of Unmodified mRNA for Reprogramming Human Dendritic Cells and T Cells.

作者信息

Sæbøe-Larssen Stein, Sioud Mouldy

机构信息

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.

出版信息

Methods Mol Biol. 2025;2965:235-244. doi: 10.1007/978-1-0716-4742-4_10.

Abstract

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.

摘要

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。

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本文引用的文献

2
Antigen cross-presentation by dendritic cells: A critical axis in cancer immunotherapy.
Semin Immunol. 2024 Feb;71:101848. doi: 10.1016/j.smim.2023.101848. Epub 2023 Nov 29.
3
Chemical Modifications of mRNA Ends for Therapeutic Applications.
Acc Chem Res. 2023 Oct 17;56(20):2814-2826. doi: 10.1021/acs.accounts.3c00442. Epub 2023 Oct 2.
4
An engineered T7 RNA polymerase that produces mRNA free of immunostimulatory byproducts.
Nat Biotechnol. 2023 Apr;41(4):560-568. doi: 10.1038/s41587-022-01525-6. Epub 2022 Nov 10.
5
Clinical advances and ongoing trials on mRNA vaccines for cancer treatment.
Lancet Oncol. 2022 Oct;23(10):e450-e458. doi: 10.1016/S1470-2045(22)00372-2.
6
Recent Advances in Modified Cap Analogs: Synthesis, Biochemical Properties, and mRNA Based Vaccines.
Chem Rec. 2022 Aug;22(8):e202200005. doi: 10.1002/tcr.202200005. Epub 2022 Apr 14.
7
Modifications of mRNA vaccine structural elements for improving mRNA stability and translation efficiency.
Mol Cell Toxicol. 2022;18(1):1-8. doi: 10.1007/s13273-021-00171-4. Epub 2021 Sep 20.
9
An origin of the immunogenicity of in vitro transcribed RNA.
Nucleic Acids Res. 2018 Jun 1;46(10):5239-5249. doi: 10.1093/nar/gky177.
10
mRNA-based therapeutics--developing a new class of drugs.
Nat Rev Drug Discov. 2014 Oct;13(10):759-80. doi: 10.1038/nrd4278. Epub 2014 Sep 19.

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