Phototheranostic Metal-Phenolic Networks with Antiexosomal PD-L1 Enhanced Ferroptosis for Synergistic Immunotherapy
Sun Yat-sen University · University of Macau · +4 more institutions
Abstract
Tumor-derived exosome can suppress dendritic cells (DCs) and T cells functions. Excessive secretion of exosomal programmed death-ligand 1 (PD-L1) results in therapeutic resistance to PD-1/PD-L1 immunotherapy and clinical failure. Restored T cells by antiexosomal PD-L1 tactic can intensify ferroptosis of tumor cells and vice versa. Diminishing exosomal suppression and establishing a nexus of antiexosomal PD-L1 and ferroptosis may rescue the discouraging antitumor immunity. Here, we engineered phototheranostic metal-phenolic networks (PFG MPNs) by an assembly of semiconductor polymers encapsulating ferroptosis inducer (Fe3+) and exosome inhibitor (GW4869). The PFG MPNs elicited superior near-infrared II…
Citation impact
- FWCI
- 23.40
- Percentile
- 100%
- References
- 38
Authors
13Topics & keywords
- Chemistry
- Exosome
- Cancer research
- Immunotherapy
- Microvesicles
- PD-L1
- Immunogenic cell death
- Dendritic cell
- Good health and well-being
Funding
- NNNational Natural Science Foundation of ChinaAwards: 32171318, 32101069
- SAScience and Technology Development FundAwards: 0103/2021/A, 0113/2019/A2, 0109/2018/A3, 0011/2019/AKP
- UDUniversidade de MacauAward: SRG2018-00130-FHS
- STScience, Technology and Innovation Commission of Shenzhen MunicipalityAward: SGDX20201103093600004