Previously, a relative resistance of solid tumor cells to immunologic effec
tor cells was shown in vitro. This resistance could be one reason for the c
linical phenomenon of resistance of patients with colon carcinoma or other
solid tumors to immunologic therapeutic approaches, In this study, dendriti
c cells (DCs) pulsed with CA 19-9 protein were rested for their immunostimu
latory capacity of immunologic effector cells against cells derived from co
lon and pancreatic carcinoma. Dendritic cell cultures coexpressed CMRF-44 a
nd CD1a, markers typical of DCs, in 31.5% +/- 5.3% after 13 days of culture
. Coculture of NK-like T lymphocytes with DCs led to a significant increase
in cytotoxic activity, as measured using a lactate dehydrogenase release a
ssay. Cytotoxic activity could be further increased using DCs pulsed with C
A 19-9 protein. The effect of CA 19-9 on increasing the cytotoxic effect of
NK-like T lymphocytes was dose dependent. Similarly, cocultivation of DCs
with NK-like T cells derived from patients with metastatic pancreatic cance
r and elevated CA 19-9 serum levels led to a significant increase in cytoto
xic activity. In conclusion, DCs pulsed with CA 19-9 protein can increase t
he cytotoxic activity of immunologic effector cells against colon carcinoma
and pancreatic cancer cells, Dendritic cells pulsed with CA 19-9 protein m
ay have an important effect on immunotherapeutic protocols for patients wit
h cancer.