September 30, 2006

HCV RNA detected by TMA

Hepatitis C virus RNA can be detected by PCR-based test

Health & Medicine Week - Oct. 02, 2006

A study from the United States has reported that hepatitis C virus (HCV) RNA was detected by TMA during the hepatitis C antiviral long-term treatment against cirrhosis (Halt-C) trial.

"For making treatment decisions related to chronic hepatitis C, the utility of HCV RNA tests with increased sensitivity has not been defined," wrote C. Morishima and colleagues, University of Washington.

"Prior interferon nonresponders with advanced fibrosis (n=1,145) were retreated with peginterferon alpha-2a and ribavirin. Patients who were HCV RNA-negative by a polymerase chain reaction (PCR)-based assay (Roche COBAS Amplicor HCV Test, v. 2.0; lower limit of detection [LOD] 100 IU/mL) at week 20 (W20) received treatment for 48 weeks.

"Stored specimens were tested using the Bayer VERSANT HCV RNA Qualitative (TMA) Assay (LOD 9.6 IU/mL) and compared to PCR results for the ability to predict sustained virological response (SVR, defined as undetectable HCV RNA by PCR at W72)," the investigators explained.

"Nearly all PCR-positive samples (1006/1007, 99.9%) were positive as assessed by TMA. Among 1,294 PCR-negative samples, 22% were TMA-positive. Negative TMA results were more predictive of SVR than were negative PCR results at W12 (82% vs. 64%, p<.001) and at W20 (66% vs. 52%, p=.001). SVR was more likely the earlier TMA had become negative during treatment (82% at W12, 44% at W20, 20% at W24). "Among 45 patients who were TMA-positive but were PCR-negative at W20 and W24, none achieved SVR (95% CI: 0%-8%). Approximately 10% of patients with a single positive TMA result at the end of treatment still achieved SVR," the researchers observed. The authors concluded, "Negative TMA results at or after W12 were superior to negative PCR results for predicting SVR. In patients with negative PCR results during treatment, a single positive TMA test did not exclude SVR, although persistently positive tests did."

Morishima and colleagues published the results of their research in Hepatology (HCV RNA detection by TMA during the hepatitis C antiviral long-term treatment against cirrhosis (Halt-C) trial. Hepatology, 2006;44(2):360-367). For additional information, contact C. Morishima, University of Washington, Department of Laboratory Medicine, Box 359690, Seattle, WA 98104, USA. The publisher of the journal Hepatology can be contacted at: John Wiley & Sons Inc., 111 River St., Hoboken, NJ 07030, USA.

September 22, 2006

Positive data for hepatitis C DNA vaccine

Tripep reports positive data for hepatitis C DNA vaccine using Inovio's DNA delivery system

Inovio Biomedical Corporation (INO) announced that its partner, Tripep AB, Sweden, has reported added positive preclinical results showing its ChronVac-C DNA vaccine using Inovio's MedPulser DNA delivery system produced a strong immune response against hepatitis C virus (HCV) in a large animal model.

Ongoing toxicity studies of ChronVac-C delivered using Inovio's electroporation-based system showed that the combination induces a humoral response in rabbits that is comparable to results previously observed in mice.

Hepatitis is a disease characterized by inflammation of the liver. Hepatitis C virus (HCV) is a major cause of acute hepatitis. HCV is spread primarily by direct contact with human blood, the major causes worldwide being the use of unscreened blood transfusions, and re-use of needles and syringes that have not been adequately sterilized. As many as 70-90% of newly infected patients may progress to develop chronic infection (WHO: 2002). Of those with chronic liver disease, 5-20% may develop cirrhosis. About 5% of infected persons may die from the consequences of long term infection (due to liver cancer or cirrhosis).

Globally, an estimated 170 million people are chronically infected with HCV, which represents a reservoir sufficiently large for HCV to persist, and 3 to 4 million persons are newly infected each year. In the U.S., while new incidences of HCV have dropped dramatically, an estimated 4.1 million (1.6%) Americans have been infected with HCV, of whom 3.2 million are chronically infected (U.S. Centers for Disease Control and Prevention: 2006).

ChronVac-C is designed to be a therapeutic DNA vaccine that can stimulate the body's immune system. Animal experiments have demonstrated that ChronVac-C vaccination activates B cells and T-cells, the latter being regarded as the most significant to clearing the chronic infection relating to hepatitis C, that killed cells producing HCV protein. In humans, the ChronVac-C DNA plasmid would be injected into muscle tissue, where vaccinations are usually given, and taken up by muscle cells with the assistance of Inovio's electroporation-based DNA delivery system. These muscle cells would be expected to then produce predetermined proteins that may activate the body's immune system to attack all cells producing HCV proteins.

Tripep AB is a Swedish biotechnology research company that develops and commercialises candidate drugs based on patented and proprietary technologies. Its main focuses are research and clinical development of ChronVac-C.

Inovio Biomedical Corporation is a late stage biomedical company focused on commercializing its proprietary Selective Electrochemical Tumor Ablation (SECTA) therapy, which is a local treatment for solid tumors, with selective killing of cancer cells while preserving surrounding healthy tissue.

September 14, 2006

Hepatitis C Virus Genome Cloned

Near Full-Length Hepatitis C Virus Genome Cloned from Clinical Samples

Gene Therapy Weekly - Sep. 14, 2006

Sept. 14, 2006 - (NewsRx.com) -- A study from the United States has reported that near full-length hepatitis C virus (HCV) genome can be cloned from clinical samples.

"Long RT-PCR (LRP) amplification of RNA templates is sometimes difficult compared to long PCR of DNA templates. Among RNA templates, HCV represents an excellent example to challenge the potential of LRP technology due to its extensive secondary structures and its difficulty to be readily cultured in vitro," wrote X.F. Fan and colleagues, St. Louis University.

"The only source for viral genome amplification is clinical samples in which HCV is usually present at low titers. We have created a comprehensive optimization protocol that allows robust amplification of a 9.1 kb fragment of HCV, followed by efficient cloning into a novel vector. Detailed analyses indicate the lack of potential LRP-mediated recombination and the preservation of viral diversity," the authors reported.

The researchers concluded, "Thus, our LRP protocol could be applied for the amplification of other difficult RNA templates and may facilitate RNA virus research such as linked viral mutations and reverse genetics."

Fan and colleagues published their study in Biochemical and Biophysical Research Communications (Efficient amplification and cloning of near full-length hepatitis C virus genome from clinical samples. Biochem Biophys Res Commun, 2006;346(4):1163-1172).

For more information, contact X.F. Fan, St. Louis University, School of Medicine, Division of Gastroenterology & Hepatology, Center Liver, Department of Internal Medicine, St. Louis, MO 63110, USA.

Publisher contact information for the journal Biochemical and Biophysical Research Communications is: Academic Press Inc. Elsevier Science, 525 B St., Ste. 1900, San Diego, CA 92101-4495, USA.

September 13, 2006

Pot helps cure hepatitis C


By jrichman@angnewspapers.com

Medical marijuana users are more likely to finish hepatitis C treatment and so are more likely to be cured, according to a newly published study conducted in San Francisco and Oakland.

Other studies have shown marijuana relieves symptoms, but medical marijuana advocates said this could be the first to show improved cure rates for a life-threatening illness.

The study is by researchers at the University of California, San Francisco, and the Oakland-based Organization to Achieve Solutions in Substance Abuse (OASIS). It was published in the European Journal of Gastroenterology and Hepatology. It found marijuana users being treated for HCV three times more likely to have a "sustained virological response," meaning the virus can't be detected six months after treatment ends.

HCV treatment with ribavirin and interferon causes severe side effects, so many patients quit the long regimen too early.

Of 71 HCV patients studied, 21 finished with a sustained virological response: 12 of the 22 cannabis users and nine of the 49 nonusers.

"Modest cannabis use may offer symptomatic and virological benefit to some patients... by helping them maintain adherence to the challenging medication regimen," the study concluded.

Rob Kampia, executive director of the Marijuana Policy Project in Washington, D.C., issued a news release touting this as "a landmark study, showing that medical marijuana can literally save lives. Every day that our government continues punishing the sick for using this medicine is literally a crime against humanity."




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Additional Info:

Sometimes the disease remains at a point where it can be managed by lifestyle changes rather than medication — and that means giving up alcohol.

"Alcohol and hep C are a witches brew," said Dr. Rick Permutt, a gastroenterologist in Santa Rosa who developed its hepatitis C clinic 10 years ago. "It fuels the fire. Those who have hep C and are drinking go to complications sooner. You already have this disease insulting your liver, why add something more?"

September 06, 2006

T Cell-based Hepatitis C Vaccines

New Perspectives for T Cell-based Hepatitis C Vaccines Are the Focus of Review

Vaccine Weekly - Aug. 30, 2006

Aug. 30, 2006--(NewsRx.com) -- A researcher reviews new perspectives for T-cell-based hepatitis C vaccines in a recent issue of the Journal of Hepatology.

According to the review, "Three percent of the world's population is chronically infected with the hepatitis C virus (HCV) and at risk of developing liver cancer. Effective cellular immune responses are deemed essential for spontaneous resolution of acute hepatitis C and long-term protection. Here, we describe a new T-cell HCV genetic vaccine capable of protecting chimpanzees from acute hepatitis induced by challenge with heterologous virus."

"Suppression of acute viremia in vaccinated chimpanzees occurred as a result of massive expansion of peripheral and intrahepatic HCV-specific CD8+ T lymphocytes that cross-reacted with vaccine and virus epitopes," said Carlo Ferrari at the University of Parma.

"These findings show that it is possible to elicit effective immunity against heterologous HCV strains by stimulating only the cellular arm of the immune system, and suggest a path for new immunotherapy against highly variable human pathogens like HCV, HIV, or malaria, which can evade humoral responses," stated the author.

Ferrari published the review in the Journal of Hepatology (New perspectives for T-cell-based HCV vaccines. J Hepatol, 2006;45(1):163-165).

For more information, contact Carlo Ferrari, Division of Infectious Diseases and Hepatology, Azienda Ospedaliero-Universitaria di Parma, I-43100 Parma, Italy. E-mail: cafer@tin.it.

Publisher contact information for the Journal of Hepatology is: Elsevier Science BV, PO Box 211, 1000 AE Amsterdam, The Netherlands.

Keywords: Parma, Italy, Hepatitis C Vaccine, Vaccine Development, Vaccine Efficacy, Hepatitis C Virus, Hepatology, Immunology, Immunotherapy, Liver Cancer Vaccine, Oncology, Virology.