| Literature DB >> 29771487 |
Rong Yang1, Jun Xu1, Ligeng Xu1, Xiaoqi Sun1, Qian Chen1, Yuhuan Zhao1, Rui Peng1, Zhuang Liu1.
Abstract
Tumor vaccines for cancer prevention and treatment have attracted tremendous interests in the area of cancer immunotherapy in recent years. In this work, we present a strategy to construct cancer vaccines by encapsulating immune-adjuvant nanoparticles with cancer cell membranes modified by mannose. Poly(d,l-lactide- co-glycolide) nanoparticles are first loaded with toll-like receptor 7 agonist, imiquimod (R837). Those adjuvant nanoparticles (NP-R) are then coated with cancer cell membranes (NP-R@M), whose surface proteins could act as tumor-specific antigens. With further modification with mannose moiety (NP-R@M-M), the obtained nanovaccine shows enhanced uptake by antigen presenting cells such as dendritic cells, which would then be stimulated to the maturation status to trigger antitumor immune responses. With great efficacy to delay tumor development as a prevention vaccine, vaccination with such NP-R@M-M in combination with checkpoint-blockade therapy further demonstrates outstanding therapeutic efficacy to treat established tumors. Therefore, our work presents an innovative way to fabricate cancer nanovaccines, which in principle may be applied for a wide range of tumor types.Entities:
Keywords: cancer cell membrane; cancer immunotherapy; checkpoint blockade; mannose modification; vaccination
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Year: 2018 PMID: 29771487 DOI: 10.1021/acsnano.7b09041
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881