Hønnåshagen Turid Kirsti, Skoge Lisbeth Johanne, Sæbøe-Larssen Stein, Håkenstad Hege, Kvalheim Gunnar, 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;2965:245-258. doi: 10.1007/978-1-0716-4742-4_11.
Dendritic cells (DCs) are the most potent antigen-presenting cells (APCs) and play a crucial role in antitumor immunity. Consequently, various strategies have been explored to utilize DCs as therapeutic vaccines, leveraging their ability to target tumor cells. A variety of antigen formulations were tested to evaluate their efficacy in vaccination, including purified tumor-associated antigens, synthetic polypeptides, and mRNA encoding tumor-associated antigens or neoantigens. In this protocol, we describe the ex vivo generation of dendritic cells from peripheral blood mononuclear cells and loading with in vitro transcribed mRNA for vaccination purposes under Good and Manufacturing Practices.
树突状细胞(DCs)是最有效的抗原呈递细胞(APCs),在抗肿瘤免疫中发挥着关键作用。因此,人们探索了各种策略来利用DCs作为治疗性疫苗,利用它们靶向肿瘤细胞的能力。测试了多种抗原制剂以评估其在疫苗接种中的功效,包括纯化的肿瘤相关抗原、合成多肽以及编码肿瘤相关抗原或新抗原的mRNA。在本方案中,我们描述了在良好生产规范下,从外周血单核细胞体外生成树突状细胞并加载体外转录的mRNA用于疫苗接种的方法。