抗原
铁蛋白
CTL公司*
细胞毒性T细胞
癌症免疫疗法
佐剂
免疫疗法
肿瘤抗原
癌症研究
免疫检查点
CD8型
免疫系统
医学
免疫学
化学
生物化学
内科学
体外
作者
Wenjun Wang,Zhida Liu,Xiaoxiao Zhou,Zhenqian Guo,Jing Zhang,Ping Zhu,Sheng Yao,Mingzhao Zhu
标识
DOI:10.1016/j.nano.2018.11.009
摘要
Recently, tumor neoantigens have been attractive for development of personal therapeutic vaccines. However, how to instantly deliver multiple neoantigens for efficient anti-tumor immunity is still challenging. Here, we established a SpyCatcher-modified ferritin nanoparticle platform, which permits convenient and stable covalent conjugation with tumor specific antigens containing SpyTag in a click-link manner. These ferritin nanoparticles are rapidly drained to lymph nodes and target dendritic cells, especially CD8α+ population, upon subcutaneous immunization. Ferritin nanoparticles carrying HPV16 oncogene E7 peptide antigen or MC38 tumor derived mutant neoantigens elicit about 2-3 folds enhanced antigen-specific cytotoxic T lymphocyte (CTL) response than soluble peptide antigens and significantly suppress the growth of E7-related or MC38 tumors. The anti-tumor effect was further enhanced in combination with PD-1 checkpoint blockade. Together, our study provides a ferritin nanoparticle-based, SpyTag/SpyCatcher-enabled click vaccine platform, especially for personalized tumor immunotherapy.
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