Bacterial outer membrane vesicle-based cancer nanovaccines

被引:0
|
作者
Xiaoyu Gao [1 ,2 ]
Qingqing Feng [1 ]
Jing Wang [3 ]
Xiao Zhao [1 ,2 ,4 ]
机构
[1] CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety & CAS Center for Excellence in Nanoscience,National Center for Nanoscience and Technology of China
[2] University of Chinese Academy of Sciences
[3] Center of Drug Evaluation, National Medical Products Administration
[4] IGDB-NCNST Joint Research Center, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences
基金
中国国家自然科学基金; 北京市自然科学基金; 国家重点研发计划;
关键词
D O I
暂无
中图分类号
R73-36 [治疗实验];
学科分类号
摘要
Tumor vaccines, a type of personalized tumor immunotherapy, have developed rapidly in recent decades. These vaccines evoke tumor antigen-specific T cells to achieve immune recognition and killing of tumor cells. Because the immunogenicity of tumor antigens alone is insufficient, immune adjuvants and nanocarriers are often required to enhance anti-tumor immune responses. At present, vaccine carrier development often integrates nanocarriers and immune adjuvants. Among them, outer membrane vesicles(OMVs) are receiving increasing attention as a delivery platform for tumor vaccines. OMVs are natural nanovesicles derived from Gramnegative bacteria, which have adjuvant function because they contain pathogen associated molecular patterns. Importantly, OMVs can be functionally modified by genetic engineering of bacteria, thus laying a foundation for applications as a delivery platform for tumor nanovaccines. This review summarizes 5 aspects of recent progress in, and future development of, OMV-based tumor nanovaccines: strain selection, heterogeneity, tumor antigen loading, immunogenicity and safety, and mass production of OMVs.
引用
收藏
页码:1290 / 1300
页数:11
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