Cervical cancer is one of the most common causes of cancer-related death in
women. As a result of several recent advances in molecular biology, the as
sociation between human papillomavirus (HPV) infection and cervical cancer
has been firmly established, and the oncogenic potential of certain HPV typ
es has been clearly demonstrated. Several lines of evidence suggest the imp
ortance of the host's immune response, especially cellular immune response,
in the pathogenesis of HPV-associated cervical lesions. These observations
form a compelling rationale for the development of vaccine therapy to comb
at HPV infection. Both prophylactic and therapeutic HPV vaccine strategies
are being developed. Prophylactic strategies currently under investigation
focus on the induction of effective humoral immune responses against subseq
uent HPV infection. In this respect, impressive immunoprophylactic effects
have been demonstrated in animals using papillomavirus-like particles (VLPs
). VLPs are antigenic and protective, but are devoid of any viral DNA that
may be carcinogenic to the host. For treatment of existing HPV infection, t
echniques to improve cellular immunity by enhancing viral antigen recogniti
on are being studied. For this purpose, the oncogenic proteins E6 and E7 of
HPV-16 and -18 are the focus of current clinical trials for cervical cance
r patients. The development of successful HPV-specific vaccines may offer a
n attractive alternative to existing screening and treatment programs for c
ervical cancer.