Dendritic cell‐targeted delivery of antigens using extracellular vesicles for anti‐cancer immunotherapy

Author:

Dang Xuan T. T.12,Phung Cao Dai12,Lim Claudine Ming Hui12,Jayasinghe Migara Kavishka12,Ang Jorgen3,Tran Thai456,Schwarz Herbert46,Le Minh T. N.12678ORCID

Affiliation:

1. Department of Pharmacology, Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore

2. Institute for Digital Medicine, Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore

3. School of Applied Science Republic Polytechnic Woodlands Singapore

4. Department of Physiology, Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore

5. Infectious Disease Translational Research Program National University of Singapore Singapore Singapore

6. Immunology Programme National University of Singapore Singapore Singapore

7. Department of Surgery, Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore

8. Institute of Molecular and Cell Biology Agency for Science, Technology, Technology and Research Singapore Singapore

Abstract

AbstractNeoantigen 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.

Funder

National University of Singapore

Publisher

Wiley

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