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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Oncolytic Viruses for Cancer Therapy: Barriers and Recent Advances
Meijun Zheng1, Jianhan Huang2, Aiping Tong3
1Department of Otolaryngology, Head and Neck Surgery, West China Hospital, West China Medical School, Sichuan University, Chengdu, Sichuan Province, P.R. China.
Abstract:
Oncolytic viruses (OVs) are powerful new therapeutic agents in cancer therapy. With the first OV (talimogene laherparepvec [T-vec]) obtaining US Food and Drug Administration approval, interest in OVs has been boosted greatly. Nevertheless, despite extensive research, oncolytic virotherapy has shown limited efficacy against solid tumors. Recent advances in viral retargeting, genetic editing, viral delivery platforms, tracking strategies, OV-based gene therapy, and combination strategies have the potential to broaden the applications of oncolytic virotherapy in oncology. In this review, we present several insights into the limitations and challenges of oncolytic virotherapy, describe the strategies mentioned above, provide a summary of recent preclinical and clinical trials in the field of oncolytic virotherapy, and highlight the need to optimize current strategies to improve clinical outcomes.
Insights
Oncolytic viruses (OVs) show promise in cancer therapy but struggle with solid tumors. Advances in viral engineering and combination strategies aim to improve their clinical efficacy for better patient outcomes.
Area of Science:
- Oncology
- Virology
- Biotechnology
Background:
- Oncolytic viruses (OVs) are emerging as potent cancer therapeutics.
- The approval of talimogene laherparepvec (T-vec) has increased interest in OV therapy.
- Current OV applications show limited efficacy against solid tumors.
Purpose of the Study:
- To review the limitations and challenges of oncolytic virotherapy.
- To describe recent advances and strategies to improve OV efficacy.
- To summarize preclinical and clinical trials and highlight optimization needs.
Main Methods:
- Review of recent scientific literature on oncolytic viruses.
- Analysis of advancements in viral retargeting and genetic editing.
- Evaluation of viral delivery platforms, tracking, gene therapy, and combination strategies.
Main Results:
- Despite progress, significant challenges remain in treating solid tumors with OVs.
- Novel strategies including viral retargeting, genetic engineering, and combination therapies show potential.
- Recent trials indicate a need for optimized strategies to enhance clinical outcomes.
Conclusions:
- Oncolytic virotherapy holds great promise but requires further optimization for solid tumors.
- Advancements in technology and strategic combinations are key to broadening OV applications.
- Future research should focus on refining OV strategies to improve patient treatment efficacy.
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