Cytotoxic T lymphocytes (CTLs) kill neoplastic or virally infected cel
ls after recognizing on their surface antigenic peptides bound to majo
r histocompatibility complex class molecules. These peptides are deriv
ed from antigens that are degraded in the cytosol of the affected cell
. Because exogenous proteins cannot enter the cytosol, immunizations w
ith killed pathogens or their proteins do not generally elicit CTLs. H
owever, antigens that are internalized into phagocytic cells can enter
the cytosol and be processed for class presentation. Here we show tha
t immunization with a purified antigen on an avidly phagocytized parti
cle primes CTLs, which in turn protect animals from subsequent challen
ge with tumours transfected with the antigen gene. Interestingly, thes
e animals also become immune to other antigens expressed by the tumour
. This approach could be exploited to develop tumour and viral vaccine
s.