This study explored the use of cytokine gene-modified tumor cells as c
ellular vaccines for the treatment of bladder cancer. The mouse MBT-2
tumor is an excellent model for human bladder cancer. This carcinogen-
induced tumor of bladder origin resembles human bladder cancer in its
etiology and histology and responds to treatment in a manner similar t
o that of its human counterpart. In a previous study we have shown tha
t interleukin 2 (IL-2)-secreting, irradiated, MBT-2 cell preparations
were capable of curing animals from orthotopically established tumors
and engendered protective immunological memory in the cured animals. I
n this study we have compared the effectiveness of several cytokines a
nd found that while IL-1 alpha, IL-1 beta, and gamma-interferon were o
nly weakly effective in the therapeutic vaccination protocol, granuloc
yte-macrophage colony-stimulating factor was almost as effective as bu
t not superior to IL-2, as reported previously for another tumor model
system. Induction of cytotoxic T-lymphocyte correlated only poorly wi
th the therapeutic benefit of the cytokine gene-modified tumor cell pr
eparations, questioning its prognostic value for the development of im
proved genetically modified tumor vaccines.