Expression of a murine interleukin 3 gene in murine fibrosarcoma cells
(FSA-JmIL-3) did not alter their survival after in vitro irradiation,
However, FSA-JmIL-3 tumors established in vivo were much more sensiti
ve to irradiation than was the parental tumor. Following 25 Gy of irra
diation, parental fibrosarcoma tumors regrew after a growth delay of 1
0 days, but FSA-JmIL-3 tumors continued to regress, Examination of the
cellular composition of tumors following irradiation revealed that, i
nstead of tumor cell repopulation, the FSA-JmIL-3 tumors became heavil
y infiltrated with lymphocytes, indicating that the effect of irradiat
ion was to allow the IL-3-elicited cellular immune response to infiltr
ate the tumors and mediate rejection, This study indicates that combin
ing gene immunotherapy approaches with radiotherapy might increase the
effectiveness of both, and it seems logical to pursue such treatment
options.