Hepatitis C virus Credits: Robin Wulffson, MD
January 30, 2012
Robin Wulffson, M.D. LA Health Examiner
Hepatitis C is a disease that impacts approximately 160 million individuals worldwide; it can lead to liver cancer and cirrhosis. Researchers from UCLA’s Jonsson Comprehensive Cancer Center have identified a cell-permeable peptide that inhibits a hepatitis C virus protein and blocks viral replication. The finding could lead to a new treatment for the disease. Senior author Dr. Samuel French, an assistant professor of pathology and senior author of the study, and his team published their results January 30 in the peer-reviewed journal Hepatology. It builds on previous work by the French laboratory that identified two cellular proteins that are important factors in hepatitis C virus infection.
French and his team initially set out to identify the cellular factors involved in hepatitis C replication and, using mass spectrometry, found that heat shock proteins (HSPs) 40 and 70 were important for viral infection. HSP70 was previously known to be involved; however, Dr. French noted that HSP40 was linked for the first time to hepatitis C infection. The researchers further showed that the natural compound Quercetin, which inhibits the synthesis of these proteins, significantly inhibits viral infection in tissue culture.
In the study, the researchers demonstrated that the viral non-structural protein 5A (NS5A) directly binds to HSP70 and mapped the site of the NS5A/HSP70 complex on NS5A. While HSP70 was previously shown to bind NS5A in cells, a direct NS5A/HSP70 interaction and complex formation was established in this study. In an effort to stop this interaction, they tested peptides that might inhibit HSP70.
“This is important because we’ve developed a small peptide that binds to that site and blocks the interaction between the proteins that is important for viral replication,” French said. “This is another, potentially highly efficacious way to block replication of hepatitis C.”
Conventional treatments for hepatitis C, interferon and ribavirin, can have significant side effects. A new drug targeting cellular proteins rather than viral proteins would be a valuable addition to the treatment arsenal, noted Dr. French. He explained, “We were surprised that this peptide works this well. While its mechanism is different, the activity of this peptide is comparable to other newly developed anti-virals.”
The study, done in tissue culture, shows that the peptide gains entry into the cell easily and blocks the cascade of cellular events that allows the virus to replicate, French said. Blocking the HSP70 protein rather than a viral protein also reduces the chance of patients with the hepatitis C virus developing resistance to the peptide.
“There’s no direct pressure on the virus, so it is less likely to mutate and develop resistance,” Dr. French said. “The goal is to achieve a sustained response, essentially a cure, meaning there is no more virus replication. There are a lot of drugs coming out now that are designed to stop hepatitis C replication, but resistance is still an issue. About 10-20% of patients on the new drugs become resistant. This new peptide may help combat resistance.”
Going forward, Dr. French and his team are testing variants of the newly discovered peptide to see if they can develop one with an even higher affinity and can decrease the size of the peptide to improve cellular penetration and liver targeting. The new and improved peptides will be tested in animal models.
This peptide “may be a candidate for hepatitis C therapy,” the study states. “Considering the potency of the peptide in suppressing viral translation levels, treatment with this peptide may significantly improve the efficacy of conventional treatments in patients who become resistant to conventional therapies.”
The study was supported in part by the National Institutes of Health and by the California Center for Antiviral Drug Discovery at the University of California.
No comments:
Post a Comment