Persistent T cell activation and cytotoxicity against glioblastoma following single oncolytic virus treatment in a clinical trial
Summary
A recent first-in-human clinical trial demonstrated that survival in glioblastoma (GBM) patients following rQNestin34.5v.2 oncolytic virus treatment was associated with immune activation signatures. This study was registered at ClinicalTrials.gov (NCT03152318). Here, we provide in situ evidence of ongoing T cell-mediated cytotoxicity against tumor cells at late time points following single treatment, with deep and persistent T cell infiltration into tumor regions. Shorter distances between
Content
# Persistent T cell activation and cytotoxicity against glioblastoma following single oncolytic virus treatment in a clinical trial
*Published: 2026 Mar 5*
A recent first-in-human clinical trial demonstrated that survival in
glioblastoma (GBM) patients following rQNestin34.5v.2 oncolytic virus treatment
was associated with immune activation signatures. This study was registered at
ClinicalTrials.gov (NCT03152318). Here, we provide in situ evidence of ongoing T
cell-mediated cytotoxicity against tumor cells at late time points following
single treatment, with deep and persistent T cell infiltration into tumor
regions. Shorter distances between cleaved caspase-3+ tumor cells and granzyme
B+ T cells were associated with longer progression-free survival following
treatment. Pre-existing tumor-infiltrating T cells expanded locally upon
treatment, correlating with longer overall patient survival. T cells with an
early activation program closely interacted with tumor cells and were strongly
enriched upon treatment. Viral remnants were restricted to necrotic regions,
while T cells infiltrated deeply into live tumor regions. These data demonstrate
that single oncolytic virus treatment can expand pre-existing T cell clones and
trigger persistent T cell-mediated immunity against GBM.
DOI: 10.1016/j.cell.2025.12.055