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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Oncolytic myxoma virus and engineering strategies for advanced cancer immunotherapy
A D Trujillo Yeriomenko1, A S Isaeva1,2, E E Idota1
1First Moscow State Medical University (Sechenov University), Moscow 119048, Russia.
Abstract:
In cancer immunotherapy, oncolytic viruses (OVs) offer an alternative approach to kill malignant cells by inducing cancer-specific host immune system activation. Given the ongoing need for safe and effective viral vectors for immunotherapy, non-zoonotic animal viruses have attracted significant interest. Here, we review the oncolytic myxoma virus (MYXV) and emphasize its emerging role in cancer immunotherapy. We critically discuss recent advances in cancer therapy using MYXV, primarily focused on engineered viral modifications. Furthermore, we briefly review alternative delivery strategies for MYXV and its combination with other anticancer agents. We also compare several key features of MYXV with those of other well-characterized OVs. In this study, we explore the key preclinical milestones that must be achieved for the MYXV OV to successfully transition to clinical trials. Preclinical studies have indicated the promising oncolytic potential and satisfactory safety profile of MYXV, thus paving the way for human clinical trials.
Insights
Oncolytic myxoma virus (MYXV) shows promise as a cancer immunotherapy agent. Preclinical studies indicate its potential for killing cancer cells and a favorable safety profile, supporting its move toward human clinical trials.
Area of Science:
- Virology
- Immunology
- Oncology
Background:
- Oncolytic viruses (OVs) are a promising cancer immunotherapy approach.
- Non-zoonotic animal viruses are of significant interest for developing safe viral vectors.
- Myxoma virus (MYXV) is an emerging OV with potential in cancer therapy.
Purpose of the Study:
- To review recent advances in MYXV-based cancer therapy.
- To discuss engineered viral modifications and delivery strategies for MYXV.
- To evaluate MYXV's potential for clinical translation in cancer immunotherapy.
Main Methods:
- Review of recent literature on MYXV in cancer therapy.
- Analysis of engineered MYXV modifications and delivery systems.
- Comparison of MYXV with other established oncolytic viruses.
Main Results:
- MYXV demonstrates promising oncolytic potential.
- Preclinical studies suggest a satisfactory safety profile for MYXV.
- Engineered MYXV modifications and alternative delivery strategies are advancing its therapeutic application.
Conclusions:
- MYXV is a viable candidate for cancer immunotherapy.
- Further preclinical development is crucial for MYXV's transition to clinical trials.
- MYXV shows potential for combination therapies with other anticancer agents.
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