A vaccine, which provides future hope for medical protection from hepatitis C, has been developed by University of Copenhagen scientists.
In this type of hepatitis the virus hides in the liver and can cause cirrhosis and liver cancer. Since the virus mutates strongly, there is no traditional vaccine to protect against it.
"The hepatitis C virus (HCV) has the same infection pathways as HIV," said Jan Pravsgaard Christensen, Associate Professor of Infection Immunology at the University.
Every year three or four million more people become infected and the most frequent path of infection is needle sharing among drug addicts or tattoo artists with poor hygiene, such as tribal tattoo artists in Africa and Asia.
Fifteen percent of new infections are sexually transmitted, while ten percent come from unscreened blood transfusions.
The new vaccine technology was developed by Peter J. Holst, a former PhD student now a postdoc with the Experimental Virology group, which also includes Professor Allan Randrup Thomsen and Christensen.
The technology works by stimulating and accelerating the immune system, and showing the body's defence mechanisms of the parts of the virus that are more conserved and do not mutate as fast and as often, such as the molecules on the surface of the HCV.
"We took a dead common cold virus, an adenovirus that is completely harmless and which many of us have met in childhood," Christensen said.
"We hid the gene for one of the HCV's internal molecules inside it. At the same time we attached a special molecule on the internal molecule so that when the cells of the mouse body tried to take a sample, they would extract a more extensive section.
"The immune defences would then be presented with a larger section of the molecule concerned. You may say that the immune defences were given an entire palm print of the internal genes instead of just a single fingerprint," he said.
This strategy resulted in two discoveries from the team. Firstly, the mice were vaccinated for HCV in a way that meant that protection was independent of variations in the surface molecules of the virus.
Secondly, the immune defences of the mice saw such an extensive section of the internal molecule that even though some aspects of it changed, there were still a couple of impressions the immune defences could recognise and respond to.
The finding has been published in the Journal of Immunology.