Infection with high-risk human papillomavirus (HPV) types is involved in ea
rly stages of uterine-cervix cancer development. The virally encoded E6 and
E7 oncoproteins behave as tumor-specific antigens and represent targets fo
r a vaccine designed to control HPV-induced tumors, Using either proteins o
r peptides based on E6 and E7 oncoproteins of HPV16 and 18, phase I clinica
l trials of therapeutic vaccines against HPV-associated cervical cancers ha
ve recently been reported. Although the effectiveness of these vaccines can
not be evaluated in such small studies, they constitute an important step t
oward the development of therapeutic uterine-cervix cancer vaccines. A poly
tope DNA vaccination approach combined with immunomodulatory cytokines may
offer an excellent strategy to reduce the risk of relapse and metastasis fo
llowing conventional therapies.