Wh. Mcbride et al., THE EFFECTS OF CYTOKINE GENE-TRANSFER INTO TUMORS ON HOST-CELL INFILTRATION AND REGRESSION, Anticancer research, 16(3A), 1996, pp. 1139-1143
New strategies are becoming available that promise to revolutionize ca
ncer immunotherapy. Although the task of generating what is in essence
a pathogenic autoimmune anti-tumor response in the face of local and
systemic immune suppression is likely to remain a formidable one, adva
nces in molecular strategies for enhancing tumor immunity have been ma
de that show considerable promise, in particular those based on gene t
ransfer technology. For example, introduction of certain cytokine gene
s into murine tumor cells have been shown to enhance tumor immunogenic
ity and induce regression. Caution is needed in properly interpreting
the relevance of observations derived from murine models for human can
cer, but clinical trials are underway that will test the utility of cy
tokine gene therapy for cancer and that will generate data that will b
e useful for the design of future strategies. Because of the magnitude
of the problem of inducing tumor regression, it is argued that, even
if genetically engineering can be used to successfully enhance anti-tu
mor immunity, combination of such strategies with other existing conve
ntional anti-cancer therapies, that increase the effectiveness of both
, may be necessary to reliably achieve cure.