SCYNEXIS to Present Preclinical HCV Data on Novel Cyclophillin ... PR-Inside.com (Pressemitteilung), Austria - Nov 7, 2008 ... study in patients chronically infected with hepatitis C virus. Abstract 1915 entitled "The Discovery of Novel, Non-immunosuppressive Cyclosporin Ethers, ...
Individuelle Immunsuppression nach Transplantation pharmazeutische-zeitung.de, Germany - Nov 11, 2008 McAlister, VC, et al., Cyclosporin versus tacrolimus as primary immunosuppressant after liver transplantation: a meta-analysis. Am J Transplant, 2006. ...
Source: Google News
Recent News and Articles on the Keywords: hepatitis + inhibits + virus Related to the article below (Last Update: 8/7/2008)
New Treatment Therapy Helps Inhibit Hepatitis C Science Daily (press release) - Jul 31, 2008 Current therapy for patients with chronic hepatitis C virus (HCV) requires up to 48 weeks of treatment. In addition, the study showed that R1626 was well ...
US Patent Disclosures TMCnet - Jul 31, 2008 7345020, titled "Mimetics of CD4 That Inhibit Immune Responses." It covers new chemical entities relating to inhibitors of the CD4 T-cell receptor. ...
Sick and Down RedOrbit, TX - Jul 27, 2008 One of these, interferonalpha, is among the most effective drugs for patients battling cancer and the hepatitis C virus. Yet the treatment has become ...
Roche posts very good results: strong market outperformance ... Business-News, Switzerland - Jul 20, 2008 Pertuzumab inhibits the pairing of HER2 with other HER receptors, a key mechanism of tumour growth. Final results from a phase II trial in women with ...
Cancer Treatment Application of the Aethlon Hemopurifier(R ... eMediaWorld.com Newswire Press Release Distribution Service (press release), AZ - Jul 24, 2008 The paper further discusses the novel therapeutic approach of the Aethlon Hemopurifier? to capture and inhibit the spread of such immunosuppressive exosomes ...OTC:AEMD
WHITEHOUSE STATION, NJ--(BUSINESS WIRE)-- StreetInsider.com (subscription), MI - Aug 5, 2008 Most subjects had other risk factors for cancer including tobacco use, papillomavirus and active hepatitis B virus infection. It is unknown if these cancer ...
Natural Killer T Cell Activation Inhibits Hepatitis B Virus Replication In Vivo - K Kakimi, LG Guidotti, Y Koezuka, FV Chisari - Journal of Experimental Medicine, 2000 - Rockefeller Univ Press ... 2000 921-930. Original Article. Natural Killer T Cell Activation Inhibits Hepatitis B Virus Replication In Vivo. Kazuhiro Kakimi a ...
Interleukin-12 inhibits hepatitis B virus replication in transgenic mice. - VJ Cavanaugh, LG Guidotti, FV Chisari - Journal of Virology, 1997 - pubmedcentral.nih.gov ... Virol. 1997 April; 71(4): 3236?3243. Copyright notice. Interleukin-12 inhibits hepatitis B virus replication in transgenic mice. VJ ...
Small Interfering RNA Inhibits Hepatitis B Virus Replication in Mice - H Giladi, M Ketzinel-Gilad, L Rivkin, Y Felig, O … - Molecular Therapy, 2003 - nature.com Original Article. Molecular Therapy (2003) 8, 769?776; doi: 10.1016/S1525-0016(03)
00244-2. Small Interfering RNA InhibitsHepatitis B Virus Replication in Mice. ...
Interferon-inhibits replication of subgenomic and genomic hepatitis C virus RNAs - M Frese, V Schwarzle, K Barth, N Krieger, V … - Hepatology, 2002 - doi.wiley.com ... 32 For example, viral clearance during hepatitis B virus (HBV) infection has ... a
coincidence because both IFN- and TNF- directly inhibitvirus replication in HBV ...
Liver transplant patients with hepatitis C virus ( HCV ) achieved significantly better long-term viral response when taking the immunosuppressive agent Cyclosporine along with Interferon-Ribavirin combination therapy.
Cyclosporine also showed efficacy against hepatitis C virus in vitro.
Hepatitis C always recurs after liver transplantation, often damaging the new organ and rendering patients ineligible for retransplantation. To address this problem, patients with hepatitis C often undergo Interferon-Ribavirin combination therapy after receiving a liver transplant in hopes of a sustained virologic response. At the same time, of course, the patients must take immunosuppressive agents to guard against transplant rejection.
The most commonly used anti-rejection medication is Tacrolimus, although Cyclosporine is also used. The latter drug has been shown to have anti-viral activity against HIV, herpes simplex and vaccinia virus, leading researchers to speculate it might also inhibit hepatitis C virus.
To examine this hypothesis, they analyzed the impact of the drug in a liver transplant population. They also studied its effect on hepatitis C in vitro.
For the in vitro study, the researchers, led by Roberto J. Firpi, of the University of Florida, treated the HCV replicon line, GSB1, with varying doses of Cyclosporine for 48 hours and examined the results. They found that Cyclosporine reduced HCV replication by 20 percent, compared to no reduction with Tacrolimus. Furthermore, the Cyclosporine appeared to work through a different pathway compared to Interferon.
Then, the researchers retrospectively examined the cases of 115 people infected with hepatitis C who had undergone liver transplantation at the University of Florida between 1991 and November 2002 and had received Interferon-based therapy alongside their anti-rejection medications. After 48 weeks, 46 percent of the patients taking Cyclosporine had achieved a sustained virological response, compared with just 27 percent of the patients taking Tacrolimus.
" Our study suggests that Cyclosporine may play a beneficial role as primary immunosuppression for patients transplanted for HCV infection and may offer an advantage to Tacrolimus in those patients undergoing IFN-based therapy," the authors report. In addition, they confirm antiviral activity by the drug in cell cultures, having found that, "combination of Cyclosporine and Interferon achieve better antiviral effect than either one alone."
Of note, considerably more patients taking Tacrolimus had to reduce or stop the therapy due to side effects. Also of possible significance, more patients taking Cyclosporine died, mostly due to infections and hepatitis complications, though this may be attributable to a longer follow-up period for that group.
Still, the indication that Cyclosporine had novel antiviral properties invites further investigation, the authors write. A prospective randomized comparative trial between Cyclosporine and TAC should further evaluate their observations.