Faculty, Staff and Student Publications
Publication Date
10-19-2023
Journal
Nature Communications
Abstract
The recent success of mRNA therapeutics against pathogenic infections has increased interest in their use for other human diseases including cancer. However, the precise delivery of the genetic cargo to cells and tissues of interest remains challenging. Here, we show an adaptive strategy that enables the docking of different targeting ligands onto the surface of mRNA-loaded small extracellular vesicles (sEVs). This is achieved by using a microfluidic electroporation approach in which a combination of nano- and milli-second pulses produces large amounts of IFN-γ mRNA-loaded sEVs with CD64 overexpressed on their surface. The CD64 molecule serves as an adaptor to dock targeting ligands, such as anti-CD71 and anti-programmed cell death-ligand 1 (PD-L1) antibodies. The resulting immunogenic sEVs (imsEV) preferentially target glioblastoma cells and generate potent antitumour activities in vivo, including against tumours intrinsically resistant to immunotherapy. Together, these results provide an adaptive approach to engineering mRNA-loaded sEVs with targeting functionality and pave the way for their adoption in cancer immunotherapy applications.
Keywords
Humans, RNA, Messenger, Immunotherapy, Extracellular Vesicles, Glioblastoma, Electroporation
Included in
Bioinformatics Commons, Biomedical Informatics Commons, Immunotherapy Commons, Medical Cell Biology Commons, Medical Genetics Commons, Oncology Commons
Comments
Supplementary Materials
PMID: 37857647