Induction of long-lasting cytokine effect by injection of IL-12 encoding plasmid DNA

Abstract

We have recently demonstrated that DNA coding for both subunits of the murine IL-12 heterodimer exhibits a strong antimetastatic effect against B16-melanoma in C57BL/6 mice and after intratumoral injection tumor regression. Here we show that the antimetastatic effect can be detected when the DNA is injected intramuscularly 30 days before tumor cell challenge. A long-term IL-12 expression was measured for up to 50 days in the serum with a peak at day 20 amounting to about 10 ng/mL in C57BL/6 mice. CpG oligodeoxynucleotides also induce IL-12 expression, however, only for a few hours. IL-12 DNA administration induces long-lasting systemic IFN-γ production, whereas IL-4 and TNF-α levels remained undetectable. NK cell–depleted mice showed a strong but reduced expression of murine IL-12. Expression of DNA encoding human instead of murine IL-12 resulted in a significantly lower and transient expression, indicating that not plasmid-derived IL-12 production alone but the immune system of the host contributes to the long-lasting antimetastatic effect. It may be attributable to an autocrine feedback mechanism maintaining murine IL-12 expression, whereby several cell populations including NK cells are involved. Cancer Gene Therapy (2000) 7, 1557–1565