To this end, scientists from the German Cancer Research Center (DKFZ) in Heidelberg are developing a completely new vaccination concept based on a low-cost vaccine that protects from almost all known oncogenic HPV types. The project has now been chosen for funding from the Helmholtz Validation Fund. The Helmholtz Association uses this fund to support promising research projects on their way to marketable applications.
Cervical cancer, which is caused by human papillomaviruses (HPV), is the third most frequent cancer in women worldwide. More than 80 percent of cervical cancer cases are diagnosed in developing countries, mainly in Africa and South America. Although currently available vaccines are efficient, they also have drawbacks: They are thermosensitive and therefore require uninterrupted cold-chain storage and transportation. In some countries, this is a logistic problem. In addition, their production is laborious and costly and they protect only against some of the cancer-causing HPV types. “Our big goal is to increase vaccination rates against HPV worldwide, particularly in low-resource countries,” said DKFZ’s Martin Müller. “Our new thermostable vaccine, which has low production costs and protects against all oncogenic HPV types, is a first, major step towards this goal.”
“The money from the Helmholtz Validation Fund is an important support in order to advance this project to marketability,” commented DKFZ’s Chairman and Scientific Director, Michael Baumann. “We thereby contribute to making this protective vaccination better available in countries where it is most urgently needed.”
The main thing for us is that the vaccine will be developed to marketability and used for the benefit of women all over the worldMartin Müller
The vaccination approach developed by Müller differs considerably from currently available vaccines. Müller chose the viral L2 protein as a starting point for the vaccine. This protein is identical in all oncogenic HPV types. However, it fails to elicit a strong immune protection. Therefore, Müller used a bacterial molecule as a scaffold to which he coupled the HPV protein in order to increase its immunogenicity. The fusion product is produced in E.coli bacteria. The trick behind this approach is that the scaffold molecule originates from an extremely thermostable archaebacterium. “Therefore, we can very easily purify the vaccination protein at high temperatures; all other E.coli proteins die in the process,” said Müller about the advantages of the new method.
In experiments with mice, Müller has already shown that the vaccine protects against infection with oncogenic HPV. The toxicological studies required for its approval are currently ongoing. Preclinical results suggest that the vaccine can protect against almost 99 percent of all HPV-induced cases of cervical cancer. In addition, it may potentially also protect against other HPV types that cause skin diseases as well as cancer of the oropharynx and anal cancer.
The financial support from the Helmholtz Validation Fund will now be used to manufacture the vaccine in pharmaceutical quality and test it in a phase 1 clinical trial. To this end, the DKFZ virologists are collaborating with renowned experts at the Moffitt Cancer Center in Florida, U.S.A. Their goal is to validate the vaccine’s tolerability and to examine whether it stimulates the production of protective antibodies in humans. “Once clinical testing of the vaccine is successfully completed, we will have to give the project into other hands,” Müller said. “For a research institution like the DKFZ, it is impossible to advance vaccine development without an industrial partner.” Since the vaccine candidate will have major advantages particularly for the poorer countries of the world, it is also possible that a nonprofit institution such as the WHO can be gained as a sponsor. “The main thing for us is that the vaccine will be developed to marketability and used for the benefit of women all over the world.”
Source: German Cancer Research Center