Abstract
IL-18 is a novel cytokine that induces interferon (IFN) -γ secretion and plays an important role in antitumor immunity. In the present study, we constructed plasmid vectors encoding the murine mature IL- 18 cDNA linked with the Igκ leader sequence and the pro-IL-18 cDNA to estimate the efficacy of the mature IL-18 vector and to evaluate IL-18-producing tumor cells as a tumor vaccine. Colon 26 cells were transfected with the abovementioned vectors or with vector alone (mock). Reverse transcription-polymerase chain reaction analysis showed increased expression of murine IL-18 cDNA in both mature IL-18 and pro-IL-18 transfectants in comparison to that in mock transfected cells. The ability of the culture supernatants of mature IL-18 transfectants to induce IFN-γ secretion was extremely high (40-140 pg/106 cells) in comparison to that of pro-IL-18 transfectants (4-18 pg/106 cells). When injected into syngeneic BALB/c mice, the growth of mature IL-18 transfectants, but not pro-IL-18 transfectants, was significantly less than that in mock transfected cells (P+ and anti-CD8+ antibodies. These data suggest that the rejection of mature IL-18/colon 26 cells was mediated through T-cell activation. Gene therapy using mature IL-18 transfectants containing a plasmid vector and the Igκ leader sequence may be a useful tumor vaccine.
Original language | English (US) |
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Pages (from-to) | 9-16 |
Number of pages | 8 |
Journal | Cancer Gene Therapy |
Volume | 8 |
Issue number | 1 |
State | Published - 2001 |
Externally published | Yes |
Keywords
- Gene therapy
- IL-18
- Immunotherapy
- Plasmid
ASJC Scopus subject areas
- Cancer Research
- Genetics