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Updated: Sep 9, 2025

Growth, Purification, and Titration of Oncolytic Herpes Simplex Virus
Published on: May 13, 2021
Oncolytic Herpes Simplex Virus Therapy: Latest Advances, Core Challenges, and Future Outlook
Yiyang Zheng1, Yusheng Pei1, Chunyan Dong1
1State Key Laboratory of Drug Regulatory Sciences, National Institutes for Food and Drug Control, Beijing 102629, China.
Abstract:
Oncolytic virus (OV) immunotherapy, particularly with oncolytic herpes simplex virus (oHSV), has become a promising new strategy in cancer treatment. This field has achieved significant clinical milestones, highlighted by the FDA approval of Talimogene laherparepvec (T-VEC) for melanoma in 2015 and the approval of Teserpaturev/G47Δ for malignant glioma in Japan in 2021. This review synthesizes the key preclinical and clinical advancements in oHSV therapy over the last decade, critically analyzing the core challenges in target selection, genetic modification, administration routes, and targeted delivery. Key findings indicate that arming oHSV with immunomodulatory transgenes, such as cytokines and antibodies, and combining it with immune checkpoint inhibitors are critical strategies for enhancing therapeutic efficacy. Future research will focus on precision engineering using CRISPR/Cas9, the development of novel delivery vehicles like nanoparticles and mesenchymal stem cells (MSCs), and biomarker-guided personalized medicine, aiming to provide safer and more effective solutions for refractory cancers. This review synthesizes oHSV advances and analyzes novel delivery and gene-editing strategies.
Insights
Oncolytic herpes simplex virus (oHSV) therapy shows promise in cancer treatment, with key strategies including genetic modification and combination therapies. Future research focuses on precision engineering and novel delivery systems for improved efficacy in refractory cancers.
Area of Science:
- Oncology
- Virology
- Immunotherapy
Background:
- Oncolytic virus (OV) therapy, specifically oncolytic herpes simplex virus (oHSV), is an emerging cancer treatment strategy.
- Clinical milestones include FDA approval of Talimogene laherparepvec (T-VEC) and Teserpaturev/G47Δ.
Purpose of the Study:
- Synthesize preclinical and clinical advancements in oHSV therapy over the past decade.
- Analyze challenges in target selection, genetic modification, administration, and delivery.
- Review novel delivery vehicles and gene-editing strategies for oHSV.
Main Methods:
- Literature review of preclinical and clinical studies on oHSV therapy.
- Analysis of genetic modification techniques and delivery systems.
- Evaluation of combination strategies with immunomodulatory transgenes and immune checkpoint inhibitors.
Main Results:
- Arming oHSV with immunomodulatory transgenes (cytokines, antibodies) enhances therapeutic efficacy.
- Combining oHSV with immune checkpoint inhibitors is a critical strategy for improved outcomes.
- Novel delivery vehicles like nanoparticles and mesenchymal stem cells (MSCs) show potential.
Conclusions:
- oHSV therapy is a promising strategy for refractory cancers.
- Precision engineering with CRISPR/Cas9 and biomarker-guided personalized medicine are future research directions.
- Developing safer and more effective oHSV-based treatments is the primary goal.
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