材料科学
启动(农业)
抗原呈递
表位
癌症免疫疗法
抗原处理
免疫疗法
抗原
癌症
获得性免疫系统
T细胞
细胞
癌症研究
免疫系统
免疫学
生物
生物化学
发芽
植物
遗传学
作者
Yao Jiang,Nishta Krishnan,Jiarong Zhou,Sanam Chekuri,Xiaoli Wei,Ashley V. Kroll,Chun Lai Yu,Yaou Duan,Weiwei Gao,Ronnie H. Fang,Liangfang Zhang
标识
DOI:10.1002/adma.202001808
摘要
Abstract The recent success of immunotherapies has highlighted the power of leveraging the immune system in the fight against cancer. In order for most immune‐based therapies to succeed, T cell subsets with the correct tumor‐targeting specificities must be mobilized. When such specificities are lacking, providing the immune system with tumor antigen material for processing and presentation is a common strategy for stimulating antigen‐specific T cell populations. While straightforward in principle, experience has shown that manipulation of the antigen presentation process can be incredibly complex, necessitating sophisticated strategies that are difficult to translate. Herein, the design of a biomimetic nanoparticle platform is reported that can be used to directly stimulate T cells without the need for professional antigen‐presenting cells. The nanoparticles are fabricated using a cell membrane coating derived from cancer cells engineered to express a co‐stimulatory marker. Combined with the peptide epitopes naturally presented on the membrane surface, the final formulation contains the necessary signals to promote tumor antigen‐specific immune responses, priming T cells that can be used to control tumor growth. The reported approach represents an emerging strategy that can be used to develop multiantigenic, personalized cancer immunotherapies.
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