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A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
Published on: May 10, 2022
[Present and future of therapy against hepatitis C]
Insights
Hepatitis C virus (HCV) infection affects 3% of the global population, with many developing chronic illness. Emerging host-targeted therapies offer new hope for effective HCV treatment and overcoming resistance.
Area of Science:
- Hepatology and Viral Immunology
- Infectious Diseases and Virology
Context:
- Hepatitis C virus (HCV) infection impacts approximately 3% of the global population, frequently leading to chronic disease.
- Current treatments, including interferon-alpha (IFN-α) and ribavirin, have limitations, with up to 50% of patients showing poor response.
- The advent of direct-acting antiviral (DAA) drugs, such as ledipasvir plus sofosbuvir approved in 2014, has significantly improved treatment efficacy, offering a potential IFN- and ribavirin-free curative option.
Purpose:
- To review the current landscape of Hepatitis C virus (HCV) treatment, highlighting the limitations of existing therapies and the emergence of new therapeutic strategies.
- To explore the potential of host-targeted therapy as a novel approach for managing HCV infection.
- To discuss the theoretical benefits of host-targeted therapy, including expanded treatment options and increased genetic barriers against viral resistance.
Summary:
- HCV infection is a significant global health concern, with a substantial portion of infected individuals developing chronic conditions.
- While DAA therapies have revolutionized HCV treatment, high costs remain a barrier. Host-targeted therapy presents a promising alternative or complementary strategy.
- Combining conventional treatments with host-targeted approaches may offer synergistic benefits, enhancing treatment outcomes and preventing the emergence of drug-resistant HCV variants.
Impact:
- Host-targeted therapy represents a paradigm shift in HCV management, potentially increasing treatment accessibility and effectiveness.
- This approach could lead to the development of novel therapeutic regimens with improved efficacy and a higher genetic barrier to resistance.
- The successful implementation of host-targeted therapies could significantly improve the long-term prognosis for patients with chronic HCV infection and contribute to disease eradication efforts.
Abstract:
Around 3% of the human population is infected with hepatitis C virus (HCV) and 70-80% of these individuals develop a chronic infection. There is no vaccine available against HCV and up to 50% of the infected patients do not respond to standard therapy, based on the combination of interferon-alpha (IFN-α) and ribavirin. Recently, direct acting antiviral drugs against HCV have been made available for treatment, leading to a significant improvement in therapeutic success. In 2014, the U.S. Food and Drug Administration approved ledipasvir plus sofosbuvir to treat the chronic infection, the first IFN- and ribavirin-free approved treatment. With such treatment, the eradication of the disease would be feasible, although drug costs are high. Host target therapy represents an emerging alternative, based on the understanding of host factors involved in the HCV infection. This therapy might show at least two theoretical benefits, increasing the number of options for therapy and raising the genetic barrier for selection of resistant variants. New treatment regimens may consist of classical therapy combined with host target-based therapy, hopefully in a synergistic manner.
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