Review Article

Physiological Role of Plasmacytoid Dendritic Cells and Their Potential Use in Cancer Immunity

Table 1


TumorSystemDC sourceProtocolReferences

EG7 T-cell lymphomaMurineExpanded in vivo (FLt3L), and sorted from BMCpG-activated OVAp-pulsed pDCs/mDCsLou et al. [109] (2007)

K17-35-OVA melanomaMurineIsolated TIDCs from K17-35 melanomaOVA-pulsed TIDCsPreynat-Seauve et al. [110] (2006)

C26 colon CarcinomaMurineIsolated TIDCs from C26 tumorTIDCs activated with CpG + anti-IL-10R (i.p.)Vicari et al. [111] (2002)

M3 MelanomaMurineā€”Topical application ImiquimodPalamara et al. [46] (2004)

Melanoma cell linesHumanSorted from PBMCpDCs activated with CD40L-transfected J558Salio et al. [42] (2003)

Melanoma stage IIIb/c, IVHumanā€”CpG-7909 (s.c.) (ProMune)Pashenkov et al. [112] (2006)

DCs, dendritic cells; pDCs, plasmacytoid DCs; BM, bone-marrow; OVAp, OVA peptide; TIDCs, tumor-infiltrating DCs (myeloid and plasmacytoid); PBMC, peripheral blood mononuclear cells.