Dendritic cells (DCs) can be used as an antigen presentation platform for v
accination against cancer. In this approach, DCs are expanded in vitro from
monocyte-derived progenitors, and subsequently loaded with well-characteri
zed tumor-associated antigens (TAAs). TAAs can be incubated with DCs in var
ious forms, including peptides, recombinant proteins, plasmid DNA, formulat
ed RNA, or recombinant viruses. Advantages and limitations of DC-based cell
ular vaccines against cancers, as well as preliminary results of clinical s
tudies already performed in humans, are discussed. Importantly, significant
advances in our understanding of the biology of DCs can be used to support
the design of new vaccines or adjuvants in order to elicit T(H)1 cellular
immune responses.