Computer search for probable T-epitopes of hepatitis A virus capsid pr
oteins was performed using an integrated set of programs. Eight segmen
ts of the VP1, VP2, VP3 and VP4 proteins were chosen and synthesised.
Five peptides previously examined as probable B-epitopes were used as
well. All the peptides were tested for their ability to stimulate prol
iferation of lymph node T-cells primed with synthetic peptides. Almost
all predicted T-epitopes affected the T-cell proliferation. None of t
he peptides had mitogenic activity. We demonstrated that regions 17-33
and 276-298 of VP1 are possible immunodominant promiscuous sites acti
vating lymphocytes of all mouse haplotypes.