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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Orf Virus-Based Therapeutic Vaccine for Treatment of Papillomavirus-Induced Tumors
M Schneider1, M Müller2, A Yigitliler1
1University Hospital Tuebingen, Institute for Medical Virology and Epidemiology of Viral Diseases, Tuebingen, Germany.
Abstract:
Orf virus (ORFV) represents a suitable vector for the generation of efficient, prophylactic antiviral vaccines against different pathogens. The present study investigated for the first time the therapeutic application of ORFV vector-based vaccines against tumors induced by cottontail rabbit papillomavirus (CRPV). ORFV-CRPV recombinants were constructed expressing the early CRPV gene E1, E2, E7, or LE6. In two independent experiments we used in total 23 rabbits which were immunized with a mixture of the four ORFV-CRPV recombinants or empty ORFV vector as a control 5 weeks after the appearance of skin tumors. For the determination of the therapeutic efficacy, the subsequent growth of the tumors was recorded. In the first experiment, we could demonstrate that three immunizations of rabbits with high tumor burden with the combined four ORFV-CRPV recombinants resulted in significant growth retardation of the tumors compared to the control. A second experiment was performed to test the therapeutic effect of 5 doses of the combined vaccine in rabbits with a lower tumor burden than in nonimmunized rabbits. Tumor growth was significantly reduced after immunization, and one vaccinated rabbit even displayed complete tumor regression until the end of the observation period at 26 weeks. Results of delayed-type hypersensitivity (DTH) skin tests suggest the induction of a cellular immune response mediated by the ORFV-CRPV vaccine. The data presented show for the first time a therapeutic potential of the ORFV vector platform and encourage further studies for the development of a therapeutic vaccine against virus-induced tumors.IMPORTANCE Viral vectors are widely used for the development of therapeutic vaccines for the treatment of tumors. In our study we have used Orf virus (ORFV) strain D1701-V for the generation of recombinant vaccines expressing cottontail rabbit papillomavirus (CRPV) early proteins E1, E2, LE6, and E7. The therapeutic efficacy of the ORFV-CRPV vaccines was evaluated in two independent experiments using the outbred CRPV rabbit model. In both experiments the immunization achieved significant suppression of tumor growth. In total, 84.6% of all outbred animals benefited from the ORFV-CRPV vaccination, showing reduction in tumor size and significant tumor growth inhibition, including one animal with complete tumor regression without recurrence.
Insights
Orf virus (ORFV) recombinant vaccines expressing cottontail rabbit papillomavirus (CRPV) genes show therapeutic potential against CRPV-induced tumors. Vaccinated rabbits experienced significant tumor growth inhibition, with some showing complete regression, indicating a promising new vaccine strategy.
Area of Science:
- Veterinary Medicine
- Oncology
- Virology
Background:
- Orf virus (ORFV) is a versatile viral vector for vaccine development.
- Cottontail rabbit papillomavirus (CRPV) induces skin tumors in rabbits, serving as a model for virus-induced cancers.
- Therapeutic vaccines are crucial for treating existing tumors, but effective strategies remain limited.
Purpose of the Study:
- To investigate the therapeutic efficacy of ORFV-CRPV recombinant vaccines against CRPV-induced tumors in rabbits.
- To evaluate the potential of the ORFV vector platform for developing anti-tumor vaccines.
- To assess the immune response induced by the ORFV-CRPV vaccine.
Main Methods:
- Construction of ORFV-CRPV recombinants expressing CRPV early genes (E1, E2, E7, LE6).
- Immunization of rabbits with CRPV-induced tumors using a mixture of ORFV-CRPV recombinants or an empty ORFV vector control.
- Monitoring tumor growth and recording therapeutic efficacy over a 26-week observation period.
- Assessing cellular immune response using delayed-type hypersensitivity (DTH) skin tests.
Main Results:
- Three immunizations with ORFV-CRPV recombinants significantly retarded tumor growth in rabbits with high tumor burden.
- Five doses of the vaccine significantly reduced tumor growth in rabbits with lower tumor burden.
- One rabbit showed complete tumor regression without recurrence.
- DTH skin tests indicated the induction of a cellular immune response.
Conclusions:
- The ORFV vector platform demonstrates therapeutic potential for treating virus-induced tumors.
- ORFV-CRPV recombinant vaccines are effective in suppressing CRPV-induced tumor growth in rabbits.
- Further research is warranted to develop ORFV-based therapeutic vaccines against viral oncogenesis.
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