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Growth, Purification, and Titration of Oncolytic Herpes Simplex Virus
Published on: May 13, 2021
HSV-1 Oncolytic Viruses from Bench to Bedside: An Overview of Current Clinical Trials
Marilin S Koch1, Sean E Lawler1, E Antonio Chiocca1
1Harvey Cushing Neurooncology Research Laboratories, Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Abstract:
Herpes simplex virus 1 (HSV-1) provides a genetic chassis for several oncolytic viruses (OVs) currently in clinical trials. Oncolytic HSV1 (oHSV) have been engineered to reduce neurovirulence and enhance anti-tumor lytic activity and immunogenicity to make them attractive candidates in a range of oncology indications. Successful clinical data resulted in the FDA-approval of the oHSV talimogene laherparepvec (T-Vec) in 2015, and several other variants are currently undergoing clinical assessment and may expand the landscape of future oncologic therapy options. This review offers a detailed overview of the latest results from clinical trials as well as an outlook on newly developed HSV-1 oncolytic variants with improved tumor selectivity, replication, and immunostimulatory capacity and related clinical studies.
Insights
Oncolytic Herpes simplex virus 1 (oHSV) therapies show promise in cancer treatment. Engineered oHSV variants are advancing in clinical trials, offering new oncology options with enhanced tumor targeting and immune response.
Area of Science:
- Virology
- Oncology
- Immunotherapy
Background:
- Herpes simplex virus 1 (HSV-1) serves as a genetic foundation for oncolytic viruses (OVs) in cancer therapy.
- Engineered oHSV variants are designed to minimize neurotoxicity while maximizing anti-tumor effects and immune stimulation.
- The FDA-approved oncolytic HSV-1, talimogene laherparepvec (T-VEC), highlights the clinical potential of this approach.
Purpose of the Study:
- To review recent clinical trial outcomes for oncolytic HSV-1 therapies.
- To provide an outlook on novel HSV-1 oncolytic variants under development.
- To discuss advancements in tumor selectivity, replication efficiency, and immunostimulatory capacity of oHSV.
Main Methods:
- Review of current clinical trial data for oncolytic HSV-1.
- Analysis of newly developed HSV-1 oncolytic virus variants.
- Assessment of tumor selectivity, replication, and immunostimulatory properties.
Main Results:
- Several oHSV variants are in clinical trials, with some showing promising results.
- Ongoing research focuses on enhancing oHSV's tumor-specific activity and immune-priming capabilities.
- The landscape of oncologic therapies may expand with the successful development of new oHSV candidates.
Conclusions:
- Oncolytic HSV-1 represents a significant area of development in cancer treatment.
- Future oHSV variants aim for improved efficacy through enhanced tumor targeting and immunogenicity.
- Clinical studies are crucial for validating the therapeutic potential of these advanced oncolytic viruses.
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