"Vaccines for cancer can be good alternatives to conventional therapies that result in serious side-effects and are rarely effective against advanced disease," said Doctor Esteban Celis. "The human papillomavirus, or HPV, is known to cause 99 per cent of cervical cancers and annually causes more than 250,000 deaths worldwide." In addition, HPV is the causative agent of a large proportion of head and neck and genital cancers.
Although two approved prophylactic vaccines against strains of HPV that cause cervical cancer are now in wide use as a measure to prevent HPV infections, these vaccines cannot be used to treat HPV-induced cancers. Thus, there is a need to develop therapeutic vaccines for HPV-related tumours.
In an effort to find an effective HPV-cancer vaccine that would eliminate existing HPV-induced cancer, Celis and Doctor Kelly Barrios-Marrugo of the University of South Florida, designed a peptide vaccination strategy called TriVax-HPV.
The TriVax vaccine strategy was designed to generate large numbers of cytotoxic T-cells that would seek out the proteins preferentially expressed in the tumours. The HPV16-E6 and E7 proteins function as oncogenic proteins inducing cancer. Thus a vaccine targeting these viral proteins is an "ideal candidate" to create strong immune responses, with the additional benefit of not generating autoimmune-related pathologies.
When they tested their vaccine in mice with HPV16-induced tumours, they found that TriVax containing a small synthetic fragment (peptide) of the E7 protein "induced tumour clearance in 100 percent of the treated mice" while the unvaccinated mice with HPV-induced tumours had their tumours grow "at a fast rate."
"Although the magnitude of the T-cell responses achieved with TriVax in mice is impressive," Barrios-Marrugo said," we do not know whether similar effects can be accomplished in humans."
COMPAMED.de; Source: Moffitt Cancer Centre