Related Experiment Video
Updated: May 22, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Preclinical evaluation of oncolytic vaccinia virus for therapy of canine soft tissue sarcoma
Ivaylo Gentschev1, Marion Adelfinger, Rafael Josupeit
1Genelux Corporation, San Diego Science Center, San Diego, California, United States of America.
Abstract:
Virotherapy using oncolytic vaccinia virus (VACV) strains is one promising new strategy for canine cancer therapy. In this study we describe the establishment of an in vivo model of canine soft tissue sarcoma (CSTS) using the new isolated cell line STSA-1 and the analysis of the virus-mediated oncolytic and immunological effects of two different Lister VACV LIVP1.1.1 and GLV-1h68 strains against CSTS. Cell culture data demonstrated that both tested VACV strains efficiently infected and destroyed cells of the canine soft tissue sarcoma line STSA-1. In addition, in our new canine sarcoma tumor xenograft mouse model, systemic administration of LIVP1.1.1 or GLV-1h68 viruses led to significant inhibition of tumor growth compared to control mice. Furthermore, LIVP1.1.1 mediated therapy resulted in almost complete tumor regression and resulted in long-term survival of sarcoma-bearing mice. The replication of the tested VACV strains in tumor tissues led to strong oncolytic effects accompanied by an intense intratumoral infiltration of host immune cells, mainly neutrophils. These findings suggest that the direct viral oncolysis of tumor cells and the virus-dependent activation of tumor-associated host immune cells could be crucial parts of anti-tumor mechanism in STSA-1 xenografts. In summary, the data showed that both tested vaccinia virus strains and especially LIVP1.1.1 have great potential for effective treatment of CSTS.
Insights
Oncolytic vaccinia virus (VACV) therapy shows promise for canine cancer. Two VACV strains effectively targeted canine soft tissue sarcoma cells and inhibited tumor growth in a mouse model, with one strain achieving complete regression and long-term survival.
Area of Science:
- Veterinary Oncology
- Virology
- Immunology
Background:
- Canine cancer therapy requires novel strategies.
- Oncolytic vaccinia virus (VACV) strains offer a promising approach.
- Canine soft tissue sarcoma (CSTS) is a prevalent malignancy.
Purpose of the Study:
- Establish an in vivo model for CSTS using the STSA-1 cell line.
- Evaluate the oncolytic and immunological effects of two VACV strains (LIVP1.1.1 and GLV-1h68) against CSTS.
- Assess the therapeutic potential of VACV virotherapy for canine cancer.
Main Methods:
- Utilized the STSA-1 cell line for in vitro studies.
- Developed a canine sarcoma tumor xenograft mouse model for in vivo experiments.
- Administered LIVP1.1.1 and GLV-1h68 VACV strains systemically.
- Monitored tumor growth, regression, survival rates, and intratumoral immune cell infiltration.
Main Results:
- Both VACV strains efficiently infected and destroyed STSA-1 cells in vitro.
- Systemic VACV administration significantly inhibited tumor growth in the xenograft model.
- LIVP1.1.1 treatment led to near-complete tumor regression and prolonged survival.
- VACV replication induced strong oncolysis and significant intratumoral immune cell infiltration, primarily neutrophils.
Conclusions:
- Oncolytic vaccinia virus (VACV) demonstrates significant potential for treating canine soft tissue sarcoma (CSTS).
- Direct viral oncolysis and virus-dependent immune cell activation are key anti-tumor mechanisms.
- The LIVP1.1.1 VACV strain shows particular efficacy, offering a promising therapeutic candidate for CSTS.
Related Concept Videos
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
Cancer Vaccines
Cancer vaccines come in two categories: preventive (prophylactic) and treatment (active). Preventive vaccines, such as the Human Papillomavirus (HPV) vaccine, protect against viruses that cause certain...
Preclinical Development: Overview
Tumor Immunotherapy

