The characterization of tumor-associated antigens recognized by human T lym
phocytes in a major histocompatibility complex (MHC)-restricted fashion has
opened new possibilities for immunotherapeutic approaches to the treatment
of human cancers. Dendritic cells (DC) are professional antigen presenting
cells that are well suited to activate T cells toward various antigens, su
ch as tumor-associated antigens, due to their potent costimulatory activity
. The availability of large numbers of DC, generated either from hematopoie
tic progenitor cells or monocytes in vitro or isolated from peripheral bloo
d, has profoundly changed pre-clinical research as well as the clinical eva
luation of these cells. Accordingly, appropriately pulsed or transfected DC
may be used for vaccination in the field of infectious diseases or tumor i
mmunotherapy to induce antigen-specific T cell responses. These observation
s led to pilot clinical trials of DC vaccination for patients with cancer i
n order to investigate the feasibility, safety, as well as the immunologic
and clinical effects of this approach. Initial clinical studies of human DC
vaccines are generating encouraging preliminary results demonstrating indu
ction of tumor-specific immune responses and tumor regression. Nevertheless
, much work is still needed to address several variables that are critical
for optimizing this approach and to determine the role of DC-based vaccines
in tumor immunotherapy.