Dendritic cell-targeted delivery of antigens using extracellular vesicles for anti-cancer immunotherapy.
Xuan T T DangCao Dai PhungClaudine Ming Hui LimMigara Kavishka JayasingheJorgen AngThai TranHerbert SchwarzMinh T N LePublished in: Cell proliferation (2024)
Neoantigen delivery using extracellular vesicles (EVs) has gained extensive interest in recent years. EVs derived from tumour cells or immune cells have been used to deliver tumour antigens or antitumor stimulation signals. However, potential DNA contamination from the host cell and the cost of large-scale EV production hinder their therapeutic applications in clinical settings. Here, we develop an antigen delivery platform for cancer vaccines from red blood cell-derived EVs (RBCEVs) targeting splenic DEC-205 + dendritic cells (DCs) to boost the antitumor effect. By loading ovalbumin (OVA) protein onto RBCEVs and delivering the protein to DCs, we were able to stimulate and present antigenic OVA peptide onto major histocompatibility complex (MHC) class I, subsequently priming activated antigen-reactive T cells. Importantly, targeted delivery of OVA using RBCEVs engineered with anti-DEC-205 antibody robustly enhanced antigen presentation of DCs and T cell activation. This platform is potentially useful for producing personalised cancer vaccines in clinical settings.
Keyphrases
- dendritic cells
- papillary thyroid
- regulatory t cells
- immune response
- squamous cell
- high throughput
- induced apoptosis
- risk assessment
- lymph node metastasis
- single cell
- drinking water
- binding protein
- circulating tumor
- stem cells
- amino acid
- cancer therapy
- cell free
- human health
- young adults
- cell therapy
- climate change
- case report
- childhood cancer
- nucleic acid