Koido Shigeo, Gong Jianlin
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Jikei University School of Medicine, 163-1 Kashiwa-shita, Kashiwa, Chiba, 277-8564, Japan,
Methods Mol Biol. 2015;1313:185-91. doi: 10.1007/978-1-4939-2703-6_13.
We have developed cell fusion vaccines generated with dendritic cells (DCs) and whole tumor cells to induce antigen-specific antitumor immunity. This approach allows DCs to be exposed to the entire repertoire of tumor-associated antigens (TAAs) originally expressed by the tumor cell, to process them endogenously, and to present antigenic epitopes thought the MHC class I and class II pathways to activate both CD8+ and CD4+ T cells, respectively. The therapeutic efficacy of DC/tumor fusion cell vaccines requires the improved immunogenicity of both cells. Here, we describe the strategy to generate DC/tumor fusion cells.
我们已经研发出了由树突状细胞(DCs)和完整肿瘤细胞生成的细胞融合疫苗,以诱导抗原特异性抗肿瘤免疫。这种方法使DCs能够接触到肿瘤细胞最初表达的全部肿瘤相关抗原(TAAs),在内源性地处理这些抗原,并通过MHC I类和II类途径呈递抗原表位,从而分别激活CD8+和CD4+ T细胞。DC/肿瘤融合细胞疫苗的治疗效果需要提高两种细胞的免疫原性。在此,我们描述了生成DC/肿瘤融合细胞的策略。