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Virus-host interaction mechanisms in interferon therapy for hepatitis B virus infection: recent advances
Jiebing Zhang1, Tao Lou1, Minmin Zhu1
1Department of Infectious Diseases, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, China.
Insights
Understanding host factors is key to improving interferon therapy for chronic hepatitis B (CHB). Managing these factors can enhance treatment efficacy and increase the clinical cure rate for hepatitis B virus (HBV) infection.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Chronic hepatitis B virus (HBV) infection leads to severe liver diseases and significant economic burden.
- Current treatments like nucleos(t)ide analogs (NAs) and interferon-α (IFN-α) have limited efficacy and cannot eliminate covalently closed circular DNA (cccDNA).
- Hepatitis B surface antigen (HBsAg) eradication and clinical cure remain challenging with existing therapies.
Purpose of the Study:
- To comprehensively review host-related factors influencing interferon therapy for chronic hepatitis B (CHB).
- To highlight the importance of understanding and managing these host factors for improved treatment outcomes.
- To explore strategies for enhancing the clinical cure rate of hepatitis B.
Main Methods:
- Literature review of studies on host factors affecting interferon therapy for CHB.
- Analysis of existing data on the efficacy and limitations of current CHB treatments.
- Synthesis of information on host- and viral-related factors impacting IFN treatment outcomes.
Main Results:
- Host factors significantly influence the efficacy of interferon therapy in CHB patients.
- Suboptimal therapeutic outcomes and complications are associated with current IFN-based treatments.
- Monotherapy with novel antiviral drugs is currently insufficient for achieving a clinical cure.
Conclusions:
- Managing host-related factors is crucial for optimizing interferon treatment efficacy in CHB.
- Addressing these factors can minimize adverse reactions and improve patient tolerance.
- Enhanced understanding and management of host factors hold the potential to increase the clinical cure rate for hepatitis B.
Abstract:
Chronic hepatitis B virus (HBV) infection has been implicated in the development of liver diseases, such as hepatitis, fibrosis, cirrhosis, and cancer, which negatively affect the patients' quality of life and impacts a high economic strain on patients. The persistence of covalently closed circular DNA (cccDNA) allows the propagation of the infection, and no drug have been developed to completely eliminate cccDNA. The available drugs for chronic hepatitis B (CHB) are classified into nucleos(t)ide analogs (NAs) and interferon-α (IFN-α)/pegylated interferon α (Peg-IFN-α). However, these treatments do not effectively eradicate hepatitis B surface antigen (HBsAg) and their clinical efficacy is limited. The potential of IFN-based clinical cure is increasingly attracting interest from hepatologists, but the therapeutic outcomes of this intervention are suboptimal and some of them are associated with various complications. Although several novel antiviral drugs are being investigated, however, achieving a clinical cure based on monotherapy is currently challenging. The efficacy of IFN therapy is influenced by host and viral factors. This article provides a comprehensive review of host-related factors that affect the IFN therapy for CHB. A thorough understanding and management of these host-related factors will enhance the efficacy of interferon treatment, minimize adverse reactions, improve patient tolerance, and thereby increasing the clinical cure rate of hepatitis B.
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