Reporting this week in the journal Nature Communications, the researchers described how a polio-rhinovirus chimera (PVSRIPO), modified to express a mutate tumor antigen found in DMG, is able to infect and induce the activity of dendritic cells.
Dendritic cells prime tumor antigen-specific T-cells to migrate to the tumor site, attack tumor cells, delay tumor growth and enhance survival in animal tumor models. But their activity can be difficult to control.
"Polioviruses have several advantages for generating antigen-specific CD8 T-cells as a potential cancer vaccine vector," said senior author Matthias Gromeier, M.D., who developed the poliovirus-based therapy as a member of Duke's Preston Robert Tisch Brain Tumor Center.
"They have naturally evolved to have a relationship with the human immune system, activating dendritic cells, inducing CD8 T-cell immunity and eliciting inflammation. As a result, they lack interference with innate or adaptive immunity."
Gromeier said the vaccine approach continues to be tested with the goal of initiating a phase 1 clinical trial.
"We are hopeful that this approach could be tested as a potential therapy for DMG tumors, which exact a terrible burden on children and their families," Gromeier said.
In addition to Gromeier, study authors Mubeen M. Mosaheb, Elena Y. Dobrikova, Michael C. Brown, Yuanfan Yang, Jana Cable, Hideho Okada, Smita K. Nair, Darell D. Bigner and David M. Ashley.
The work received support from the Public Health Service (R01 NS108773, F32 CA224593), a Defeat DIPG Research Grant and the V Foundation.
Authors Gromeier, Dobrikova, Brown, Nair, Bigner and Ashley are co-inventors of intellectual property for the PVSRIPO therapy that was licensed to Istari Oncology.
Mubeen M Mosaheb, Elena Y Dobrikova, Michael C Brown, Yuanfan Yang, Jana Cable, Hideho Okada, Smita K Nair, Darell D Bigner, David M Ashley, Matthias Gromeier.
Genetically stable poliovirus vectors activate dendritic cells and prime antitumor CD8 T cell immunity.
Nature Communications volume 11, Article number: 524, 2020. doi: 10.1038/s41467-019-13939-z.