articleJournal of the American Chemical SocietyJan 5, 2022Closed access

Phototheranostic Metal-Phenolic Networks with Antiexosomal PD-L1 Enhanced Ferroptosis for Synergistic Immunotherapy

Sun Yat-sen University · University of Macau · +4 more institutions

PubMed
Indexed incrossrefpubmed

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

287
total citations
FWCI
23.40
Percentile
100%
References
38
Citations per year

Authors

13

Topics & keywords

Keywords
  • Chemistry
  • Exosome
  • Cancer research
  • Immunotherapy
  • Microvesicles
  • PD-L1
  • Immunogenic cell death
  • Dendritic cell
UN Sustainable Development Goals
  • Good health and well-being
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