Related Experiment Video
Updated: Jan 31, 2026

Growth, Purification, and Titration of Oncolytic Herpes Simplex Virus
Published on: May 13, 2021
Therapeutic Effect on Bladder Cancer with a Conditionally Replicating Oncolytic Virus Derived from Type II Herpes
Kwan Joong Joo1,2, Hongtao Li3,4,5, Xiaoliu Zhang3,4,6,7
1Scott Department of Urology, Baylor College of Medicine, Houston, TX, USA.
Purpose:
Despite recent improvements, resistance to traditional immunotherapy or chemotherapy is still common in patients with bladder cancer. We constructed an oncolytic virus from herpes simplex virus type II (HSV-2), which selectively targets tumor cells with an activated Ras signaling pathway. We evaluated the antitumor effect of this oncolytic HSV-2 (FusOn-H2) against bladder cancer, and compared with that of a first generation oncolytic virus derived from HSV-1 (Baco-1).
Materials And Methods:
We established bladder tumor at the orthotopic site in C3H/He mice using the MBT-2 cells. Baco-1 or FusOn-H2 was instilled into the bladder through the urethra respectively. Tumor volume and weight were recorded by the end of the experiment. Animal spleens were also collected to determine if any anti-tumor immunity was elicited during virotherapy in this syngeneic bladder cancer model.
Results:
Two instillations of the oncolytic HSVs into bladder of tumor-bearing mice almost completely eradicated the tumor in majority of tumor bearing mice. The results of tumor-specific cytotoxic T lymphocyte activity assay showed that tumor destruction by oncolytic viruses in vivo, especially by the FusOn-H2, induced potent anti-tumor immune responses.
Conclusion:
Oncolytic virus derived from HSV-2 has potent anti-tumor activity against bladder cancer. Oncolytic effect of this virus in vivo induces tumor specific cellular immunity that further enhances the overall anti-tumor activity. Translating this novel virotherapy into the clinic could present an alternative intravesical therapy strategy for patients with bladder cancer.
Insights
A novel oncolytic virus from herpes simplex virus type II (HSV-2), FusOn-H2, demonstrated potent anti-tumor activity against bladder cancer in mice. This virotherapy also induced significant anti-tumor immunity, offering a promising new treatment strategy.
Area of Science:
- Oncolytic virotherapy
- Cancer immunology
- Herpes simplex virus vectors
Background:
- Bladder cancer remains challenging due to resistance to conventional therapies.
- Oncolytic viruses offer a targeted approach to cancer treatment.
- Herpes simplex virus (HSV) is a promising platform for oncolytic virus development.
Purpose of the Study:
- To evaluate the antitumor efficacy of a novel HSV-2-derived oncolytic virus (FusOn-H2) against bladder cancer.
- To compare FusOn-H2 with an existing HSV-1-derived oncolytic virus (Baco-1).
- To assess the immunogenicity of FusOn-H2 in a preclinical bladder cancer model.
Main Methods:
- An orthotopic bladder cancer model was established in C3H/He mice using MBT-2 cells.
- Oncolytic viruses (Baco-1 or FusOn-H2) were administered via intravesical instillation.
- Tumor volume, weight, and spleen immune cell activity were analyzed post-treatment.
Main Results:
- Intravesical instillation of FusOn-H2 and Baco-1 led to near-complete tumor eradication in most treated mice.
- FusOn-H2 induced potent tumor-specific cytotoxic T lymphocyte responses.
- Oncolytic virotherapy, particularly with FusOn-H2, effectively stimulated anti-tumor immunity.
Conclusions:
- Oncolytic HSV-2 demonstrates significant potential as a treatment for bladder cancer.
- The induced tumor-specific cellular immunity enhances the overall therapeutic effect.
- FusOn-H2 represents a promising intravesical virotherapy strategy for bladder cancer patients.
Related Concept Videos
What are Viruses?
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
Introduction to Virus
Viruses of Archaea
Viruses with RNA Genomes
Intracellular Movement of Viruses and Bacteria

