A new approach to T cell epitope determination is presented. Critical
amino acids for the induction of cytotoxic T cell responses were ident
ified using synthetic peptide libraries with single defined sequence p
ositions combined with randomized sequence positions, Sequences for po
tential T cell epitopes were deduced from scan profiles using combinat
ions of the active amino acids. Highly potent epitopes for cytotoxic T
lymphocytes were obtained. Epitopes defined by this approach are, as
shown in this communication, not necessarily the natural epitopes and,
therefore, were named synthetic epitopes. They can serve effectively
for the development of vaccines or for the determination of T cell rec
eptor antagonists.