Researchers at Mass General Brigham, USA, have modified a herpes simplex virus (HSV-1) that stimulates the immune system to attack glioblastoma cells.
A single dose of the modified virus increased T-cell, natural killer cell, and myeloid cell responses in the tumour microenvironment and increased the overall survival in preclinical models.
Results are published in Nature Cancer.
Glioblastoma is among the most aggressive and treatment-resistant brain tumours.
Previous attempts to stimulate the immune system to attack tumour cells in the brain have shown limited benefit, in part because glioblastoma cells release multiple molecules that dampen immune responses.
To overcome the barriers, researchers modified an HSV-1 virus to recognise markers found only on glioblastoma cells.
They engineered the virus to express five different immunomodulatory molecules to help reprogram the tumour environment, including IL-12, anti-PD1, a bispecific T cell engager, 15-hydroxyprostaglandin dehydrogenase, and anti-TREM2.
Researchers also added safety mutations, or “off-switches,” that prevent the virus from spreading to neurons or healthy central nervous system cells.
So that the reach of the virus could be visualised on A PET scan, the team inserted a gene that expresses a protein capable of trapping a PET-tracer molecule.
Mice treated with the virus showed increased infiltration of tumour-fighting T cells, as well as reduced T-cell exhaustion markers.
Mice injected with the virus also lived longer than glioblastoma-harbouring mice not injected with the virus.
“We engineered a safe and traceable oncolytic virus with strong cytotoxic and immunostimulatory activities for glioblastoma immunotherapy,” said Francisco J.
Quintana, PhD, of the Mass General Brigham Department of Neurology, is and senior author on the federally funded study.
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“This platform offers a multipronged approach—precise tumour targeting, local delivery of immunotherapeutic payloads, and a built-in safety system to protect normal brain cells.”
Future research will focus on evaluating the safety and efficacy of the oncolytic virus in human trials as well as adapting the viral platform to remodel the tumour microenvironment in other cancers.
Source: Mass General Brigham
