Background: Various immunotherapeutical approaches are presently evaluated
for their efficacy to eradicate glioma cells. Complicating the concepts, th
ese tumors secrete cytokines which modulate the immune response. Materials
& Methods: We analyzed the influence of interferon gamma (IFN-gamma) on the
cytokine production and IFN-gamma receptor expression in T98G and U87-MG h
uman glioma cells. Results: The IFN-gamma receptors were own-regulated afte
r IFN-gamma treatment. Secretion of interleukin-6 (IL-6) protein was elevat
ed by factors of 6.4 in T98G cells and 5.2 in U87-MG. Other cytokines were
increased as well, brit less constantly: IL-8, and VEGF were elevated signi
ficantly only in T98G, but not in U87-MG. Increases of IL-1 beta, IL-1a and
TGF beta -2 were only detectable at the mRNA level. TNF was not detectable
in any of the cell lines, and TGF-beta, aFGF and HG were not influenced by
IFN-gamma. Conclusion: IL-6 produced by glioma cells in response to IFN-ga
mma might support immune eradication of glioma cells.