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Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
Published on: September 25, 2019
Management of chronic hepatitis B infection
Vinay Sundaram1, Kris Kowdley2
1Department of Medicine and Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Insights
Hepatitis B virus (HBV) infection remains a significant global health concern. New antiviral treatments are needed to achieve sustained viral clearance and eliminate hepatitis B surface antigen (HBsAg).
Area of Science:
- Hepatology
- Virology
- Infectious Diseases
Background:
- Hepatitis B virus (HBV) infection is a major cause of cirrhosis and hepatocellular carcinoma (HCC) worldwide.
- Despite vaccination efforts, the disease burden remains high, necessitating effective antiviral therapies.
- Current treatments reduce liver disease progression but face challenges in optimal timing, modality, and duration.
Purpose of the Study:
- To review the current landscape of Hepatitis B virus (HBV) treatment options.
- To discuss the benefits and limitations of existing antiviral drugs, including pegylated interferon and nucleos(t)ide analogs.
- To highlight the need for novel therapeutic strategies for sustained HBV DNA and HBsAg clearance.
Main Methods:
- Review of current literature on Hepatitis B virus (HBV) treatments.
- Analysis of approved antiviral agents: pegylated interferon and nucleos(t)ide analogs.
- Discussion of treatment monitoring, including hepatitis B surface antigen (HBsAg) levels.
Main Results:
- Nucleos(t)ide analogs offer good tolerability and viral suppression with low resistance risk.
- Pegylated interferon provides a finite treatment duration but may require HBsAg monitoring for response prediction.
- Prolonged oral antiviral therapy is often needed, with common relapse upon discontinuation.
Conclusions:
- Current antiviral treatments for Hepatitis B virus (HBV) are effective but have limitations.
- Optimal treatment strategies regarding timing, modality, and duration require further investigation.
- There is a critical need for new treatments that achieve sustained HBV DNA and HBsAg clearance.
Abstract:
Hepatitis B virus (HBV) is a global health problem that can lead to cirrhosis and hepatocellular carcinoma (HCC). Although HBV vaccination has reduced the prevalence Of HBV infection, the burden of disease remains high. Treatment with antiviral drugs reduces the risk of liver disease and the development of HCC, and it can even reverse liver fibrosis. However, challenges remain regarding optimal timing, as well as the modality and duration of treatment. Currently approved drugs include pegylated interferon and nucleos(t)ide analogs. Nucleos(t)ide analogs are better tolerated and provide excellent viral suppression with a low risk of antiviral resistance, but pegylated interferon offers the benefit of a finite duration of treatment. Monitoring of hepatitis B surface antigen (HBsAg) levels may help to predict the likelihood of response to treatment, particularly for pegylated interferon. Prolonged treatment is usually needed with oral antiviral agents, and relapse is common if treatment is discontinued. New treatments that result in sustained clearance of HBV DNA and the clearance of HBsAg are needed.
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