RRC ID 1900
Author Ojima T, Iwahashi M, Nakamura M, Matsuda K, Naka T, Nakamori M, Ueda K, Ishida K, Yamaue H.
Title The boosting effect of co-transduction with cytokine genes on cancer vaccine therapy using genetically modified dendritic cells expressing tumor-associated antigen.
Journal Int. J. Oncol.
Abstract The T-helper 1 (Th1) immune reaction is most important in dendritic cell (DC)-based immunotherapy. Interleukin 12 (IL-12) and granulocyte macrophage colony-stimulating factor (GM-CSF) play a pivotal role in inducing Th1 and cytotoxic T lymphocyte (CTL) responses. In this study, DCs expressing the natural tumor antigen gp70 of BALB/c-derived CT26 were adenovirally transduced with the IL-12 gene and/or GM-CSF gene, and it was examined whether vaccinations using these genetically engineered DCs can induce strong therapeutic antitumor immunity. Mice were immunized once by subcutaneous (s.c.) injection with genetically modified DCs. The cytotoxic activity of splenocytes against CT26 was assayed in a 51Cr-release assay 14 days after immunization. The therapeutic efficacy of the vaccination was examined in s.c. tumor models. The cytotoxic activity of CTLs against CT26 in mice immunized with DCs expressing gp70 (DC-AxCAgp70) was significantly augmented by co-transduction with the GM-CSF/IL-12 gene (p<0.0001) and remarkably reduced by the depletion of CD4+ or CD8+ cells (p<0.01). The cytotoxic activity against CT26 of the plain spleen cells in mice immunized with DC-AxCAgp70/GM-CSF/IL-12 was significantly higher than that in mice immunized with DC-AxCAgp70 (p<0.0001), and this activity decreased to almost 50% upon the depletion of NK cells. Vaccinations using DC-AxCAgp70/GM-CSF/IL-12 or DC-AxCAgp70/IL-12 could elicit potent therapeutic immunity in s.c. tumor models; tumor-free mice were observed in these vaccination groups. However, there was no significant difference between these two groups. A vaccination therapy using DCs co-transduced with the TAA gene and Th 1-type cytokine genes, especially the IL-12 gene, is ideal for immunotherapy in terms of the activation of DCs, NK cells, CD4+ T cells and CD8+ T cells, and may be useful in the clinical application of a cancer vaccine therapy.
Volume 28(4)
Pages 947-53
Published 2006-4
PMID 16525645
MeSH Adenoviridae / genetics Animals Antigens, Neoplasm / genetics* CD4-Positive T-Lymphocytes / immunology CD8-Positive T-Lymphocytes / immunology Cancer Vaccines / immunology* Cancer Vaccines / therapeutic use Cell Line Cell Line, Tumor Cytokines / genetics* Dendritic Cells / immunology* Dendritic Cells / metabolism Dendritic Cells / transplantation Female Gene Expression Genetic Vectors / genetics Granulocyte-Macrophage Colony-Stimulating Factor / genetics Humans Immunotherapy, Adoptive / methods* Interferon-gamma / metabolism Interleukin-12 / genetics Interleukin-12 / metabolism Killer Cells, Natural / immunology Mice Mice, Inbred BALB C Neoplasms, Experimental / immunology Neoplasms, Experimental / pathology Neoplasms, Experimental / therapy Spleen / cytology Spleen / immunology T-Lymphocytes, Cytotoxic / immunology Transfection
IF 3.333
Times Cited 29
WOS Category ONCOLOGY
Resource
DNA material AxCAmIL12p35 (RDB1414) AxCAmIL12p40 (RDB1417)