Abstract
Background:
Inadequate release of tumor antigens (TA) and a defective antigen presentation by dendritic cells (DC) are the major mechanisms for how tumor cells can escape the host immune surveillance.
Materials and methods:
Combined gene therapy of herpes simplex virus thymidine kinase (Tk), GM-CSF and IL-4 via adenoviral vector was tested to solve these problems. After establishing wild-type Lewis lung carcinoma (LLC), vaccinations with LLC transduced with Tk +/- GM-CSF +/- IL-4 were performed.
Results:
The LLC-Tk and LLC-Tk-IL-4 vaccination groups failed to suppress the wild-type LLC growth. However, the LLC-Tk-GM-CSF group showed a delayed wild-type tumor growth and LLC-Tk-GM-CSF-IL-4 markedly suppressed tumor growth and increased the survival rate of mice. Immunohistochemistry of the spleen showed a dense infiltration of DCs in the mice treated with LLC-Tk-GM-CSF-IL-4.
Conclusion:
Combined gene therapy with Tk-GM-CSF-IL-4 was effective in inducing antitumor immunity by enhancing the DC functions.
Publication types
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Evaluation Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antigen Presentation
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Antiviral Agents / therapeutic use
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Carcinoma, Lewis Lung / immunology
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Carcinoma, Lewis Lung / therapy*
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Cytomegalovirus / genetics
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Dendritic Cells / immunology
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Ganciclovir / therapeutic use
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Genetic Therapy*
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Genetic Vectors / genetics
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Genetic Vectors / therapeutic use
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Granulocyte-Macrophage Colony-Stimulating Factor / genetics*
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Granulocyte-Macrophage Colony-Stimulating Factor / physiology
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Immunologic Surveillance
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Interleukin-2 / genetics
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Interleukin-2 / physiology
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Interleukin-4 / genetics*
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Interleukin-4 / physiology
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Mastadenovirus / genetics
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Mice
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Mice, Inbred C57BL
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Neoplasm Transplantation
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Promoter Regions, Genetic
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Recombinant Fusion Proteins / physiology
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Simplexvirus / enzymology
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Simplexvirus / genetics*
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Spleen / immunology
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Thymidine Kinase / genetics*
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Thymidine Kinase / physiology
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Transduction, Genetic
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Tumor Escape
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Vaccination
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Viral Proteins / genetics*
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Viral Proteins / physiology
Substances
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Antiviral Agents
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Interleukin-2
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Recombinant Fusion Proteins
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Viral Proteins
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Interleukin-4
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Granulocyte-Macrophage Colony-Stimulating Factor
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Thymidine Kinase
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Ganciclovir