Live attenuated Salmonella as a vector for oral cytokine gene therapy in melanoma
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Updated: Jul 15, 2026

Experimental Melanoma Immunotherapy Model Using Tumor Vaccination with a Hematopoietic Cytokine
Published on: February 24, 2023
Caroline Agorio1, Fernanda Schreiber, Mark Sheppard
1Laboratory for Vaccine Research, Departamento de Desarrollo Biotecnológico, Instituto de Higiene, Facultad de Medicina, Av. Navarro 3051, Montevideo, Uruguay.
Abstract:
Systemic administration of cytokines has shown therapeutic benefits in cancer patients; however, serious adverse effects associated with direct protein administration prevent the wide use of this approach. We have assessed the capacity of live attenuated Salmonella to act as a vector for oral cytokine-gene therapy. Salmonella orally administered to melanoma-bearing mice was found to accumulate within the tumor, reaching up to 10(5) bacteria per gram of tumor by day 21 after bacterial inoculation. Numbers of bacteria recovered from tumor did not differ from those recovered from liver or spleen at any time point. Recombinant bacteria carrying eukaryotic expression vectors encoding the murine IL-4 or IL-18 genes were administered to groups of mice with established subcutaneous melanoma tumors. We found that a single oral dose of Salmonella carrying any of the cytokine-encoding plasmids resulted in significantly increased survival time, as compared with mice that received Salmonella carrying the parental plasmid or PBS. Increased levels of IFNgamma were found in sera of animals receiving either of the cytokine-encoding bacteria, but not in mice receiving Salmonella alone or PBS. Co-administration of both recombinant bacteria maximized the production of IFNgamma. Overall these results suggest that cytokine-encoding Salmonella can be an effective and safer alternative to systemic administration of cytokines for immunotherapy of cancer.
Insights
Live attenuated Salmonella bacteria were engineered to deliver cytokine genes orally for cancer immunotherapy. This approach significantly improved survival in mice with melanoma, offering a safer alternative to direct cytokine injection.
Area of Science:
- Oncology
- Immunotherapy
- Microbial Therapeutics
Background:
- Systemic cytokine administration shows cancer therapeutic potential but is limited by severe adverse effects.
- Developing safer and more effective cancer immunotherapy strategies is crucial.
Purpose of the Study:
- To evaluate live attenuated Salmonella as a vector for oral cytokine-gene therapy in cancer.
- To assess the efficacy of Salmonella-mediated interleukin-4 (IL-4) and interleukin-18 (IL-18) gene delivery in a murine melanoma model.
Main Methods:
- Oral administration of live attenuated Salmonella engineered to express murine IL-4 or IL-18 in melanoma-bearing mice.
- Quantification of bacterial load in tumors, liver, and spleen.
- Measurement of serum interferon-gamma (IFN-γ) levels.
- Assessment of survival rates.
Main Results:
- Salmonella accumulated in tumors of orally inoculated mice.
- A single oral dose of cytokine-encoding Salmonella significantly increased survival time compared to controls.
- Administration of cytokine-encoding Salmonella led to increased serum IFN-γ levels.
- Co-administration of both IL-4 and IL-18 producing Salmonella maximized IFN-γ production.
Conclusions:
- Live attenuated Salmonella can serve as an effective oral vector for cytokine gene therapy.
- Salmonella-mediated cytokine delivery represents a potentially safer alternative to systemic cytokine administration for cancer immunotherapy.
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