Laser-Activatable In Situ Vaccine Enhances Cancer-Immunity Cycle

© 2023 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 35(2023), 52 vom: 10. Dez., Seite e2307193
1. Verfasser: Wang, Zhenyu (VerfasserIn)
Weitere Verfasser: You, Tingting, Su, Qianyi, Deng, Wenjia, Li, JiaBao, Hu, Saixiang, Shi, Shengjun, Zou, Zhaowei, Xiao, Jisheng, Duan, Xiaopin
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2023
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article caner-immunity cycle immunotherapies in situ vaccine photodynamic therapy photothermal therapy B7-H1 Antigen Vaccines
Beschreibung
Zusammenfassung:© 2023 Wiley-VCH GmbH.
The immune response in cancer reflects a series of carefully regulated events; however, current tumor immunotherapies typically address a single key aspect to enhance anti-tumor immunity. In the present study, a nanoplatform (Fe3 O4 IR820@CpG)-based immunotherapy strategy that targets the multiple key steps in cancer-immunity cycle is developed: 1) promotes the release of tumor-derived proteins (TDPs), including tumor-associated antigens and pro-immunostimulatory factors), in addition to the direct killing effect, by photothermal (PTT) and photodynamic therapy (PDT); 2) captures the released TDPs and delivers them, together with CpG (a Toll-like receptor 9 agonist) to antigen-presenting cells (APCs) to promote antigen presentation and T cell activation; 3) enhances the tumor-killing ability of T cells by combining with anti-programmed death ligand 1 antibody (α-PD-L1), which collectively advances the outstanding of the anti-tumor effects on colorectal, liver and breast cancers. The broad-spectrum anti-tumor activity of Fe3 O4 @IR820@CpG with α-PD-L1 demonstrates that optimally manipulating anti-cancer immunity not singly but as a group provides promising clinical strategies
Beschreibung:Date Completed 28.12.2023
Date Revised 06.01.2024
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202307193