Ferritin nanoparticle-based SpyTag/SpyCatcher-enabled click vaccine for tumor immunotherapy

被引:87
|
作者
Wang, Wenjun [1 ,2 ]
Liu, Zhida [1 ,3 ]
Zhou, Xiaoxiao [1 ,2 ]
Guo, Zhenqian [4 ]
Zhang, Jing [5 ]
Zhu, Ping [4 ]
Yao, Sheng [5 ]
Zhu, Mingzhao [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Biophys, Key Lab Infect & Immun, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
[3] Univ Texas Southwestern Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
[4] Chinese Acad Sci, Inst Biophys, Natl Lab Biomacromol, Beijing, Peoples R China
[5] TopAlliance Biosci, Oncol & Cellular Therapy, Rockville, MD USA
基金
中国国家自然科学基金;
关键词
Ferritin nanoparticle; SpyTag/SpyCatcher; Click vaccine; Therapeutic tumor vaccine; Neoantigen; T-CELLS; THERAPY; DELIVERY; PROTEIN;
D O I
10.1016/j.nano.2018.11.009
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
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 CD8 alpha(+) 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 minor immunotherapy. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:69 / 78
页数:10
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