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Updated: May 25, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
A novel genetically modified oncolytic vaccinia virus in experimental models is effective against a wide range of
Dana Haddad1, Nanhai Chen, Qian Zhang
1Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Background:
Replication-competent oncolytic viruses have shown great promise as a potential cancer treatment. This study aimed to determine whether a novel vaccinia virus, GLV-1h151, with genetic modifications enhancing cancer specificity and enabling virus detection, is effective against a range of human cancers and is safe when administered in preclinical models.
Methods:
GLV-1h151 was modified with deletion of thymidine kinase enhancing specificity and insertion of the green fluorescent protein (GFP) gene. The virus was tested in several human cancer cell lines for cytotoxicity including breast, lung, pancreatic, and colorectal. Virus replication was assessed via visualization of GFP expression and bioluminescence, and viral plaque assays. Finally, GLV-1h151 was administered systemically or intratumorally in mice with pancreatic cancer xenografts (PANC-1) to assess virus biodistribution, toxicity, and effect on tumor growth.
Results:
GLV-1h151 effectively infected, replicated in, and killed several cancer cell types. Detection and visualization of virus replication was successful via fluorescence imaging of GFP expression, which was dose dependent. When administered intravenously or intratumorally in vivo, GLV-1h151 regressed tumor growth (P < 0.001) and displayed a good biosafety profile. GLV-1h151 infection and replication in tumors was successfully visualized via GFP and bioluminescence, with virus presence in tumors confirmed histologically.
Conclusions:
GLV-1h151 is effective as an oncolytic agent against a wide range of cancers in cell culture and is effective against pancreatic human xenografts displaying a good biosafety profile and ability to be detected via optical imaging. GLV-1h151 thus adds another potential medium for the killing of cancer and detection of virus in infected tissue.
Insights
A novel oncolytic vaccinia virus, GLV-1h151, effectively targets and destroys various cancer cells. This virus demonstrated significant tumor regression in preclinical models with a favorable safety profile, offering a promising new cancer therapy.
Area of Science:
- Oncolytic virotherapy
- Cancer research
- Viral oncology
Background:
- Replication-competent oncolytic viruses show promise for cancer treatment.
- A novel vaccinia virus, GLV-1h151, was developed with enhanced cancer specificity and detectability.
Purpose of the Study:
- To evaluate the efficacy of GLV-1h151 against diverse human cancers.
- To assess the safety of GLV-1h151 in preclinical cancer models.
Main Methods:
- GLV-1h151 was genetically modified for specificity and detection (GFP).
- Cytotoxicity assays were performed on breast, lung, pancreatic, and colorectal cancer cell lines.
- In vivo studies involved administering GLV-1h151 to pancreatic cancer xenografts in mice.
Main Results:
- GLV-1h151 demonstrated effective infection, replication, and cancer cell killing.
- Fluorescence imaging confirmed dose-dependent virus replication.
- Intravenous and intratumoral administration led to significant tumor regression (P < 0.001) with a good safety profile.
Conclusions:
- GLV-1h151 is a potent oncolytic agent against various cancers in vitro and in vivo.
- The virus exhibits a favorable safety profile and can be tracked via optical imaging.
- GLV-1h151 represents a potential new therapeutic strategy for cancer treatment.
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