R. Agger et al., Characterization of murine dendritic cells derived from adherent blood mononuclear cells in vitro, SC J IMMUN, 52(2), 2000, pp. 138-147
The therapeutic potential of dendritic cells loaded with tumour antigens fo
r the induction of effective immune responses against cancer is currently b
eing tested in numerous clinical trials. In most cases, the dendritic cells
are generated in vitro from peripheral blood monocytes. Many aspects of de
ndritic cell-based vaccination have not yet been examined in detail, and ho
mologous mouse model systems may prove very valuable for optimizing clinica
l procedures. In the murine system, however, dendritic cells are usually is
olated from either lymphoid tissues or bone marrow cultures. To date, murin
e monocyte-derived dendritic cells have been described only sporadically. H
ere, we describe a culture system for the generation of murine dendritic ce
lls from adherent peripheral blood mononuclear cells by culturing in the pr
esence of granulocyte-macrophage colony stimulating factor and interleukin-
4. After 7 days of culture the nonadherent cells were harvested from the cu
ltures. Most of these cells exhibited well-accepted characteristics of matu
re dendritic cells (e.g. veiled appearance, high expression of major histoc
ompatibility complex class II and CD86) and stimulated vigorous proliferati
on of allogeneic T cells in a primary mixed leucocyte reaction following st
imulation with bacterial lipopolysaccharide. Interestingly, staining the ce
lls for expression of the putative antigen-uptake receptor DEC-205 revealed
a distinct bimodal distribution.