Subcutaneous Nanodisc Vaccination with Neoantigens for Combination Cancer Immunotherapy

被引:68
作者
Kuai, Rui [1 ,2 ]
Sun, Xiaoqi [1 ,2 ]
Yuan, Wenmin [1 ,2 ]
Xu, Yao [1 ,2 ]
Schwendeman, Anna [1 ,2 ]
Moon, James J. [1 ,2 ,3 ]
机构
[1] Univ Michigan, Dept Pharmaceut Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Biointerfaces Inst, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
IMMUNE-RESPONSES; DELIVERY SYSTEMS; MYELOID CELLS; BLOCKADE; VACCINES; IMMUNOGENICITY; NANOPARTICLES; INJECTION; MELANOMA;
D O I
10.1021/acs.bioconjchem.7b00761
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
While cancer immunotherapy provides new exciting treatment options for patients, there is an urgent need for new strategies that can synergize with immune checkpoint blockers and boost the patient response rates. We have developed a personalized vaccine nanodisc platform based on synthetic high-density lipoproteins for co-delivery of immunostimulatory agents and tumor antigens, including tumor-specific neoantigens. Here we examined the route of delivery, safety profiles, and therapeutic efficacy of nanodisc vaccination against established tumors. We report that nanodiscs administered via the subcutaneous (SC) or intramuscular (IM) routes were well tolerated in mice without any signs of toxicity. The SC route significantly enhanced nanoparticle delivery to draining lymph nodes, improved nanodisc uptake by antigen-presenting cells, and generated 7-fold higher frequency of neoantigen-specific T cells, compared with the IM route. Importantly, when mice bearing advanced B16F10 melanoma tumors were treated with nanodiscs plus anti-PD-1 and anti-CTLA-4 IgG therapy, the combination immunotherapy exerted potent antitumor efficacy, leading to eradication of established tumors in similar to 60% of animals. These results demonstrate nanodiscs customized with patient-specific tumor neoepitopes as a safe and powerful vaccine platform for immunotherapy against advanced cancer.
引用
收藏
页码:771 / 775
页数:5
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