Although cervical carcinoma cells may express the human papillomavirus
oncoproteins E6 and E7, they fail to induce an effective specific cyt
otoxic T lymphocyte response. This failure may be due to a lack of exp
ression of costimulatory molecules, such as CD80 (B7.1). To augment th
e immunogenicity of cervical carcinoma cells, we transfected human pap
illomavirus (HPV)-transformed cell lines, CaSki and HeLa, with the CD8
0 expression vector pBJ. Alloantigens on the tumor cells were used for
the stimulation of peripheral blood lymphocytes (PBLs). Cocultivation
of PBLs and tumor cells resulted in proliferation of CD4(+) and CD8() T lymphocyte subsets. CD80-expressing tumor cells induced proliferat
ion of allogeneic PBLs two- to sixfold compared to control cell lines.
Cocultivation of allogeneic PBLs with CD80-positive tumor cells for 3
weeks gave rise to cytotoxic T cells capable of lysing untransfected
parental tumor cell lines. Our results demonstrate an immunostimulator
y effect of CD80 expression on cervical cancer cells, which provides a
basis for the development of a therapeutic tumor vaccine. (C) 1996 Ac
ademic Press, Inc.