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Dendritic cell-targeted delivery of antigens using extracellular vesicles for anti-cancer immunotherapy.
Dang, Xuan T T; Phung, Cao Dai; Lim, Claudine Ming Hui; Jayasinghe, Migara Kavishka; Ang, Jorgen; Tran, Thai; Schwarz, Herbert; Le, Minh T N.
Affiliation
  • Dang XTT; Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Phung CD; Institute for Digital Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Lim CMH; Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Jayasinghe MK; Institute for Digital Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Ang J; Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Tran T; Institute for Digital Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Schwarz H; Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Le MTN; Institute for Digital Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Cell Prolif ; 57(7): e13622, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38509634
ABSTRACT
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dendritic Cells / Ovalbumin / Cancer Vaccines / Extracellular Vesicles / Immunotherapy / Antigens, Neoplasm Limits: Animals / Humans Language: En Journal: Cell Prolif / Cell prolif / Cell proliferation Year: 2024 Type: Article Affiliation country: Singapore

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dendritic Cells / Ovalbumin / Cancer Vaccines / Extracellular Vesicles / Immunotherapy / Antigens, Neoplasm Limits: Animals / Humans Language: En Journal: Cell Prolif / Cell prolif / Cell proliferation Year: 2024 Type: Article Affiliation country: Singapore