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Updated: Jan 18, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Therapeutic vaccination for glioblastoma elicited by retargeted oncolytic herpes virus
Francesca Piaggio1, Chiara Riviera2, Francesco Alessandrini3
1IRCCS Ospedale Policlinico San Martino, Genoa, Italy francesca.piaggio@aomliguria.it paolo.malatesta@unige.it tatiana.gianni3@unibo.it.
Background:
Glioblastoma is an aggressive tumor with poor prognosis and limited treatment options due to its resistance to chemotherapy and radiotherapy, high heterogeneity, and ability to evade the immune system. Nevertheless, immunotherapy and oncolytic virotherapy are emerging as promising strategies. This study aimed to evaluate the therapeutic efficacy of an engineered oncolytic Herpes Simplex Virus for glioblastoma treatment.
Methods:
We investigated the efficacy of R-115, a retargeted oncolytic Herpes Simplex Virus directed against the human epidermal growth factor receptor 2 (HER2) and engineered to express murine interleukin-12, in an immunocompetent glioblastoma model that recapitulates HER2 tumor heterogeneity. We tested the translatability and reliability of R-115 by assessing overall survival in HER2+ or HER2+/HER2- mixed tumors treated with different schedules. We assessed the potential of the treatment to elicit an antitumor vaccination effect by rechallenging previously treated mice with HER2-negative cells in the absence of any further therapy. Additionally, we characterized both the immune and tumor components by analyzing immune cells' proliferation, activation and the resulting tumor cells reduction.
Results:
R-115 exhibited potent cytotoxic and immune-stimulatory effects, significantly prolonging survival and eradicating tumors in approximately 25% of treated mice independently from tumor composition and treatment schedule. Furthermore, it induced long-term immune memory, enabling the eradication of secondary transplanted tumors, effectively acting as a tumor-agnostic vaccination. Notably, in addition to the direct oncolysis mediated by the virus, R-115 treatment induced an immune response even against HER2-negative glioblastoma cells, potentially via cross-presentation or epitope spreading.
Conclusions:
Our findings candidate R-115 as a promising alternative to standard glioblastoma treatments and support further investigation to advance its clinical application.
Insights
An engineered oncolytic virus, R-115, shows promise for glioblastoma treatment by prolonging survival and inducing immune memory. This therapy demonstrated efficacy against HER2-positive and mixed tumors, suggesting potential as a vaccination strategy.
Area of Science:
- Oncolytic virotherapy
- Immunotherapy
- Glioblastoma research
Background:
- Glioblastoma is an aggressive brain tumor with poor prognosis.
- Current treatments are limited by resistance and tumor heterogeneity.
- Immunotherapy and oncolytic virotherapy offer promising new strategies.
Purpose of the Study:
- To evaluate the therapeutic efficacy of R-115, an engineered oncolytic Herpes Simplex Virus.
- To assess R-115 in an immunocompetent glioblastoma model with HER2 heterogeneity.
- To investigate R-115's potential for inducing antitumor immune memory.
Main Methods:
- Investigated R-115, a retargeted oncolytic Herpes Simplex Virus targeting HER2 and expressing IL-12.
- Assessed overall survival in HER2+/HER2- mixed glioblastoma models.
- Evaluated antitumor vaccination effect by rechallenging mice with HER2-negative cells.
- Analyzed immune cell proliferation, activation, and tumor cell reduction.
Main Results:
- R-115 significantly prolonged survival and eradicated tumors in 25% of mice.
- Treatment efficacy was independent of tumor composition and schedule.
- R-115 induced long-term immune memory, eradicating secondary tumors.
- An immune response against HER2-negative cells was observed, suggesting cross-presentation or epitope spreading.
Conclusions:
- R-115 is a promising candidate for glioblastoma treatment.
- The virus demonstrated both direct cytotoxic and immune-stimulatory effects.
- Further clinical investigation of R-115 is warranted.
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