Cancer vaccines are entering a new: phase of popularity, in part because of
the recognition of when a therapeutic vaccine is most effective and the in
dentification of appropriate target antigens. New technologies most notably
gene transfection into dedritic cell and DNA vaccination approaches, have
spurred further clinical evaluations. While many researchers consider humor
al responses as not being viable for large tumors , these responses may pla
y a role in regulating micrometastases (i.e., adjuvant setting. The recent
approval of antibodies as therapeutics for cancer treatment has lent to the
viability oft his therapy concept. The success of carbohydrate-conjugate v
accines in bacterial systems has also renewed interest in developing such v
accines for cancer- immunotherapy. Carbohydrates can be further converted i
nto peptide/protein mimetics with several of these mimetics in clinical tri
als. These mimetic forms can be manipulated into DNA vaccine types that may
be combined into DNA cassettes that contain CTL-associated epitopes to fil
l-ther define a novel strategy for future vaccine development.