In a study conducted at Texas Biomed's Southwest National Primate  Research Center, researchers found that the immune modulator GS-9620 (see structure below),  which targets a receptor on immune cells, reduced both the virus levels  and the number of infected liver cells in chimpanzees chronically  infected with hepatitis B virus (HBV). Chimpanzees are the only species  other than humans that can be infected by HBV. Therefore, the results  from this study were critical in moving the drug forward to human  clinical trials which are now in progress.
 The new report, co-authored by scientists from Texas Biomed and Gilead Sciences, appears in the May issue of Gastroenterology.  Gilead researchers had previously demonstrated that the same therapy  could induce a cure of hepatitis infection in woodchucks that were  chronically infected with a virus similar to human HBV.
The new report, co-authored by scientists from Texas Biomed and Gilead Sciences, appears in the May issue of Gastroenterology.  Gilead researchers had previously demonstrated that the same therapy  could induce a cure of hepatitis infection in woodchucks that were  chronically infected with a virus similar to human HBV.
"This is an important proof-of-concept study demonstrating that the  therapy stimulates the immune system to suppress the virus and eliminate  infected liver cells," said co-author Robert E. Lanford, Ph.D., of  Texas Biomed. "One of the key observations was that the therapy  continued to suppress virus levels for months after therapy was stopped.
The current therapy for HBV infection targets the virus and works  very well at suppressing viral replication and delaying progression of  liver disease, but it is a lifelong therapy that does not provide a  cure.
"This GS-9620 therapy represents the first conceptually new treatment  for HBV in more than a decade, and combining it with the existing  antiviral therapy could be transformative in dealing with this disease,"  stated Lanford.
Ref: http://www.gastrojournal.org/article/S0016-5085%2813%2900169-8/abstract?referrer=http://www.sciencedaily.com/releases/2013/04/130426152556.htm?utm_source=feedburner 
