| Literature DB >> 35410368 |
Chao Liu1, Xue Liu1, Xinchu Xiang1, Xin Pang1, Siyuan Chen1, Yunming Zhang1, En Ren1, Lili Zhang1, Xuan Liu1, Peng Lv1, Xiaoyong Wang1,2, Wenxin Luo1,2, Ningshao Xia1,2, Xiaoyuan Chen3, Gang Liu4,5,6.
Abstract
The strategy of combining a vaccine with immune checkpoint inhibitors has been widely investigated in cancer management, but the complete response rate for this strategy is still unresolved. We describe a genetically engineered cell membrane nanovesicle that integrates antigen self-presentation and immunosuppression reversal (ASPIRE) for cancer immunotherapy. The ASPIRE nanovaccine is derived from recombinant adenovirus-infected dendritic cells in which specific peptide-major histocompatibility complex class I (pMHC-I), anti-PD1 antibody and B7 co-stimulatory molecules are simultaneously anchored by a programmed process. ASPIRE can markedly improve antigen delivery to lymphoid organs and generate broad-spectrum T-cell responses that eliminate established tumours. This work presents a powerful vaccine formula that can directly activate both native T cells and exhausted T cells, and suggests a general strategy for personalized cancer immunotherapy.Entities:
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Year: 2022 PMID: 35410368 DOI: 10.1038/s41565-022-01098-0
Source DB: PubMed Journal: Nat Nanotechnol ISSN: 1748-3387 Impact factor: 40.523