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An update from Germany


Degradation of viral DNA in the cell nucleus opens new Hepatitis B treatment possibilities

Scientists from the Helmholtz Zentrum München and the Technische Universität München have discovered how the viral DNA of the hepatitis B virus (HBV) can be degraded in the cell nucleus of liver cells, consequently allowing the virus to be eliminated. Viruses such as HBV can persist by depositing their genetic information (DNA) in the cell nucleus, where the DNA is normally not degraded. This prevents antiviral drugs from eliminating these viruses. But the newly discovered mechanism could make this possible without damaging the infected cell in the liver. In the current issue of the prestigious journal Science, the scientists report that now new therapeutic possibilities are consequently opening up.

Although preventive vaccination is possible, the World Health Organization (WHO) reports that more than 240 million people around the world are currently suffering from a chronic hepatitis B infection. They face a high risk of developing liver cirrhosis or even liver cancer. In Germany alone, more than half a million people are affected. Although available antiviral medicines can control the hepatitis B virus, they cannot completely eliminate it. As a result, the HBV in the patient's liver is reactivated as soon as the treatment is discontinued.

This is due to virus DNA (cccDNA: covalently closed circular DNA) "hidden" in the cell nucleus. This virus DNA stores multiple copies of the virus in the nucleus of infected liver cells (hepatocytes) and in this way protects itself from destructive influences. The cccDNA serves as a template for the virus' own proteins and new viral genomes. An international team of scientists headed by Prof. Ulrike Protzer and Prof. Mathias Heikenwälder, Institute of Virology at the Helmholtz Zentrum München and the Technische Universität München, has now found a way to selectively attack and eliminate the viral genetic information in the cell nucleus of the liver cells without damaging the host cell in the process.

"The degradation of viral DNA in the cell nucleus that we describe represents an important mechanism in the defence against the virus", Protzer reports. "Moreover, for the first time, the results offer the possibility to develop a treatment that can heal hepatitis B."

The scientists have discovered that in addition to interferons (the immune system's defence agents), activation of the lymphotoxin β receptor in the host cell promotes certain proteins and supports their function in such a way that they chemically modulate and degrade viral cccDNA. This keeps the virus from reactivating, and also prevents the disease from breaking out again, even after the treatment has ended. On the other hand, the proteins do not influence the genetic information of the host cell itself, which here is the liver cell. "With the activation of the lymphotoxin β receptor, also combined with substances that are already available, we have a very promising new therapy concept available", Heikenwälder explains.

Explore further: Novel therapeutic approaches to cure chronic HBV infection

More information: Lucifora, J. et al. (2014), "Specific and Non-Hepatotoxic Degradation of Nuclear Hepatitis B Virus cccDNA." Science, DOI: 10.1126/science.1243462
3 Responses
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Avatar universal
Absolutely unless a large number of us unite behind this idea then we can just deal with crappy dangerous treatments that will prolong our life but won't offer a good quality of life due to their horrid side effects. Outrageous really!
Helpful - 0
Avatar universal
Well the answer is obvious. Who will they sell TDF and ETV to. So that is why nothing ever comes out from these finding.

Our disease is an industry folks. And nobody really cares. All we really have available is interferon till clear hbv. The rest real cures may never come about.
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Avatar universal
My only reservation about this is its been having journal etc issued since 2011 from what I can find and its still come to nothing tangible. My question is why???
Helpful - 0
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