| Literature DB >> 30529790 |
Wenjun Wang1, Zhida Liu2, Xiaoxiao Zhou1, Zhenqian Guo3, Jing Zhang4, Ping Zhu3, Sheng Yao4, Mingzhao Zhu5.
Abstract
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.Entities:
Keywords: Click vaccine; Ferritin nanoparticle; Neoantigen; SpyTag/SpyCatcher; Therapeutic tumor vaccine
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Year: 2018 PMID: 30529790 DOI: 10.1016/j.nano.2018.11.009
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307