The application of molecularly defined vaccines composed of a limited
number of tumor-specific T cell epitopes has resulted in protective an
titumor T cell immunity in several mouse tumor models. The first encou
raging results with such vaccines have been obtained in human beings.
The development of the next generation of rationally designed vaccines
that are both effective and safe for application in a clinical settin
g requires comparison of different modes of delivery of tumor-associat
ed T cell epitopes in multiple epitope constructs.