Gene therapy with GM-CSF, interleukin-4 and herpes simplex virus thymidine kinase shows strong antitumor effect on lung cancer

Anticancer Res. 2003 Mar-Apr;23(2B):1559-64.

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

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation
  • Antiviral Agents / therapeutic use
  • Carcinoma, Lewis Lung / immunology
  • Carcinoma, Lewis Lung / therapy*
  • Cytomegalovirus / genetics
  • Dendritic Cells / immunology
  • Ganciclovir / therapeutic use
  • Genetic Therapy*
  • Genetic Vectors / genetics
  • Genetic Vectors / therapeutic use
  • Granulocyte-Macrophage Colony-Stimulating Factor / genetics*
  • Granulocyte-Macrophage Colony-Stimulating Factor / physiology
  • Immunologic Surveillance
  • Interleukin-2 / genetics
  • Interleukin-2 / physiology
  • Interleukin-4 / genetics*
  • Interleukin-4 / physiology
  • Mastadenovirus / genetics
  • Mice
  • Mice, Inbred C57BL
  • Neoplasm Transplantation
  • Promoter Regions, Genetic
  • Recombinant Fusion Proteins / physiology
  • Simplexvirus / enzymology
  • Simplexvirus / genetics*
  • Spleen / immunology
  • Thymidine Kinase / genetics*
  • Thymidine Kinase / physiology
  • Transduction, Genetic
  • Tumor Escape
  • Vaccination
  • Viral Proteins / genetics*
  • Viral Proteins / physiology

Substances

  • Antiviral Agents
  • Interleukin-2
  • Recombinant Fusion Proteins
  • Viral Proteins
  • Interleukin-4
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Thymidine Kinase
  • Ganciclovir