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Updated: Dec 23, 2025

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Virotheranostics, a double-barreled viral gun pointed toward cancer; ready to shoot?
Mohsen Keshavarz1, Ailar Sabbaghi2, Seyed Mohammad Miri3
11The Persian Gulf Tropical Medicine Research Center, The Persian Gulf Biomedical Sciences Research Institute, Bushehr University of Medical Sciences, Bushehr, Iran.
Abstract:
Compared with conventional cancer treatments, the main advantage of oncolytic virotherapy is its tumor-selective replication followed by the destruction of malignant cells without damaging healthy cells. Accordingly, this kind of biological therapy can potentially be used as a promising approach in the field of cancer management. Given the failure of traditional monitoring strategies (such as immunohistochemical analysis (in providing sufficient safety and efficacy necessary for virotherapy and continual pharmacologic monitoring to track pharmacokinetics in real-time, the development of alternative strategies for ongoing monitoring of oncolytic treatment in a live animal model seems inevitable. Three-dimensional molecular imaging methods have recently been considered as an attractive approach to overcome the limitations of oncolytic therapy. These noninvasive visualization systems provide real-time follow-up of viral progression within the cancer tissue by the ability of engineered oncolytic viruses (OVs) to encode reporter transgenes based on recombinant technology. Human sodium/iodide symporter (hNIS) is considered as one of the most prevalent nuclear imaging reporter transgenes that provides precise information regarding the kinetics of gene expression, viral biodistribution, toxicity, and therapeutic outcomes using the accumulation of radiotracers at the site of transgene expression. Here, we provide an overview of pre-clinical and clinical applications of hNIS-based molecular imaging to evaluate virotherapy efficacy. Moreover, we describe different types of reporter genes and their potency in the clinical trials.
Insights
Oncolytic virotherapy offers tumor-selective cancer treatment. Human sodium/iodide symporter (hNIS) reporter gene imaging enables real-time monitoring of oncolytic virus (OV) efficacy and safety in preclinical and clinical studies.
Area of Science:
- Oncology
- Molecular Imaging
- Gene Therapy
Background:
- Oncolytic virotherapy (OV) offers tumor-selective cancer cell destruction, a key advantage over conventional treatments.
- Traditional monitoring methods for OV therapy lack real-time safety and efficacy assessment capabilities.
- Noninvasive molecular imaging is crucial for tracking OV progression and therapeutic outcomes in live models.
Purpose of the Study:
- To review the preclinical and clinical applications of human sodium/iodide symporter (hNIS) for molecular imaging in oncolytic virotherapy.
- To highlight the advantages of hNIS-based imaging for real-time monitoring of OV biodistribution, gene expression, and therapeutic efficacy.
- To discuss various reporter genes and their potential in clinical trials for evaluating virotherapy.
Main Methods:
- Engineered oncolytic viruses (OVs) incorporating reporter transgenes, specifically the human sodium/iodide symporter (hNIS).
- Utilizing three-dimensional molecular imaging techniques for noninvasive visualization of viral progression.
- Employing radiotracer accumulation at the site of transgene expression to assess gene kinetics and viral biodistribution.
Main Results:
- The hNIS reporter gene enables precise tracking of OV gene expression kinetics.
- hNIS-based imaging provides accurate data on viral biodistribution, toxicity, and therapeutic outcomes.
- This approach facilitates real-time monitoring of oncolytic treatment efficacy in live animal models.
Conclusions:
- hNIS-based molecular imaging is a powerful tool for evaluating oncolytic virotherapy efficacy and safety.
- This noninvasive strategy overcomes limitations of traditional monitoring methods.
- Reporter gene imaging holds significant promise for advancing oncolytic virotherapy in clinical applications.
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