The interest in the use of human dendritic cells in cancer immunothera
py calls for efficient ex vivo methods of dendritic cell education. To
extend the range of methods available, we generated phenotypically ch
aracteristic dendritic cells from peripheral blood monocytes incubated
with granulocyte-macrophage colony-stimulating factor and interleukin
-4 and infected them with an adenovirus containing a humanized version
of green fluorescent protein as a marker of gene expression. The leve
ls of expressed protein were high, but they were further increased in
combination with cationic liposomes. In comparison to transfection eff
iciency of the homologous expression plasmid, adenovirus-mediated gene
transfer was substantially more efficient. With the aid of liposome-m
ediated infection, gene transfer into CD83(+) dendritic cells was high
ly effective, resulting in more than 90% of the cells expressing the t
ransgene. (C) 1998 by The American Society of Hematology.