Abstract
Cancer vaccines have attracted tremendous interest in the field of cancer immunotherapy due to their ability to trigger tumor-specific immune responses to destroy cancer cells. Herein, we demonstrate that dendrimers coordinated with manganese ions (GT-Mn2+) could self-assemble with peptides to form a cancer vaccine, which could be internalized by dendritic cells (DCs) via specific macropinocytosis-dependent and lipid-raft-related pathways and then dissociated gradually to release peptides to achieve efficient antigen cross-presentation and stimulate the cGAS-STING pathway. Additionally, GT-Mn2+ could package multiple neoantigens to form an effective “personalized” cancer vaccine and has exhibited excellent therapeutic effects when used in combination with anti-PD-L1. Thus, our work presents an innovative peptide carrier to construct an effective “personalized” cancer vaccine that shows great promise to achieve effective cancer immunotherapy for different patients in clinic.
| Original language | English |
|---|---|
| Pages (from-to) | 3574-3597 |
| Number of pages | 24 |
| Journal | Matter |
| Volume | 6 |
| Issue number | 10 |
| DOIs | |
| State | Published - 4 Oct 2023 |
Keywords
- MAP6: Development
- Mn
- cGAS-STING pathway
- cancer vaccine
- dendrimer
- immune checkpoint blockade