Objective: To summarize existing data regarding the feasibility of dev
eloping strategies for prophylactic and therapeutic vaccination agains
t human papillomavirus (HPV) infection. Data Sources: We used the Medl
ine data base and reference lists of articles to identify English-lang
uage papers that evaluate strategies for prophylactic and therapeutic
vaccination against HPV infection. Methods of Study Selection: Our sea
rch uncovered several reports of systems that produce recombinant HPV
major capsid proteins as antigens for biochemical, molecular, and immu
nologic studies and investigations that evaluate cell-mediated immune
responses to HPV-induced, tumor-associated peptides. Data Extraction a
nd Synthesis: Recombinant HPV major capsid proteins, which self-assemb
le into virus-like particles, are produced in quantity, mimic the conf
ormation of native virions, react with neutralizing antibodies, and ar
e type-specific. Human papillomavirus early viral peptides induce cyto
toxic T lymphocyte responses that retard tumor progression and protect
against tumor development after challenge in animal models. Conclusio
ns: Recombinant papillomavirus virus-like particles are highly antigen
ic, protective in animal models, lack potentially carcinogenic viral D
NA, and are, therefore, ideal candidates for a prophylactic vaccine ag
ainst HPV infection. Immunization with HPV tumor peptides may be benef
icial in tumor prevention, regression, and rejection. Vaccines against
HPV infection can be important in reducing the incidence of cervical
dysplasia and carcinoma worldwide, particularly in developing countrie
s.