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Hepatitis B virus triggers cell 'suicide' in patients with chronic infection
9 April 2008
Scientists from UCL (University College London) have identified a key difference between people who can fight the Hepatitis B virus (HBV) off successfully and those who fail to do so - that a group of cells important in controlling the disease are triggered to 'commit suicide' in patients who are chronically infected.
The researchers analysed thousands of genes in T cells, critical players of the immune system required for control of HBV. They found that T cells from patients who were chronically infected were triggered to 'commit suicide'. This could be an important factor in determining why these patients' immune systems cannot fight the infection, and a process which could be a useful target for new treatments. Their findings are published today in the Journal of Clinical Investigation.
Hepatitis B virus (HBV) is one of the most common viruses in the world, and ranks as one of the top ten killer infectious diseases. More than 350 million people have long-term infection with HBV, which may lead to liver cirrhosis, liver failure or liver cancer. In the majority of adults infected, the immune system is able to control the virus very well and is, in fact, more effective than any currently available treatment. Understanding what goes wrong in people with chronic infection is crucial to the development of new therapies.
Lead author, Dr Mala Maini, UCL Division of Infection & Immunity, said: "We used microarray gene chips to screen more than 5,000 genes in T cells from both recovered and chronically infected Hepatitis B patients. This led to the discovery that, instead of successfully reacting to the virus, the T cells in the latter group were triggered to commit suicide by one of the cells' own death-inducing proteins, called 'Bim'. We are now looking into the fine mechanism driving this outcome."
The paper's first author, Ross Lopes, added: "If we can develop safe ways of blocking the suicidal tendency of the T cells, we may be able to prolong their survival, so they can do a better job of controlling Hepatitis B infection."
The proportion of the world's population currently infected with HBV is estimated at between 3 and 6 per cent, but up to a third have been exposed. It is endemic in parts of Asia and Africa. Chronic Hepatitis B may eventually cause liver cirrhosis and liver cancer, a fatal disease with very poor response to current treatments. The infection is preventable by vaccination at a young age.
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Notes for Editors
1. Journalists seeking more information, or interviews with the researchers quoted, can contact Ruth Metcalfe in the UCL Media Relations Office on tel: +44 (0)20 7679 9739, mobile: +44 (0)7990 675 947, out of hours: +44 (0)7917 271 364, e-mail: r.metcalfe@ucl.ac.uk
2. 'Bim-mediated deletion of antigen-specific CD8 T cells in patients unable to control hepatitis B virus' is published online ahead of print in the Journal of Clinical Investigation and is embargoed to Tuesday 8th April 2008 at 9pm GMT (5pm Eastern). Journalists can obtain copies of the paper by contacting the UCL Media Relations Office.
3. The paper's authors are from UCL Division of Infection and Immunity, UCL Centre for Sexual Health and HIV Research, Camden Primary Care Trust and the Singapore Institute for Clinical Sciences. Some of the authors receive funding from the Medical Research Council.
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