| Literature DB >> 31260255 |
Yi Wang1,2, Yao-Xin Lin1,3, Jie Wang1,2, Sheng-Lin Qiao1,2, Yu-Ying Liu4, Wen-Qian Dong4, Junqing Wang3, Hong-Wei An1,5, Chao Yang1, Muhetaerjiang Mamuti1,2, Lei Wang1, Bo Huang4, Hao Wang1,2.
Abstract
Cellular immunotherapeutics aim to employ immune cells as anticancer agents. Ex vivo engineering of dendritic cells (DCs), the initial role of an immune response, benefits tumor elimination by boosting specific antitumor responses. However, directly activating DCs in vivo is less efficient and therefore quite challenging. Here, we designed a nanoactivator that manufactures DCs through autophagy upregulating in vivo directly, which lead to a high-efficiency antigen presention of DCs and antigen-specific T cells generation. The nanoactivator significantly enhances tumor antigen cross-presentation and subsequent T cell priming. Consequently, in vivo experiments show that the nanoactivators successfully reduce tumor growth and prolong murine survival. Taken together, these results indicate in situ DCs manipulation by autophagy induction is a promising strategy for antigen presentation enhancement and tumor elimination.Entities:
Keywords: antigen presentation; autophagy; cancer immunotherapy; dendritic cell; nanoparticles
Year: 2019 PMID: 31260255 DOI: 10.1021/acsnano.9b00143
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881