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Related Concept Videos

Retrovirus Life Cycles01:10

Retrovirus Life Cycles

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Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the...
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A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
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Chronic Hepatitis B Infection: New Approaches towards Cure.

Mojisola Ogunnaike1,2, Srijanee Das1,2, Samiksha S Raut1

  • 1Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE 68198, USA.

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|August 26, 2023
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Summary

New long-acting treatments for chronic hepatitis B virus (HBV) infection show promise for improving patient adherence. These advancements include novel compounds and genome editing strategies targeting persistent viral DNA.

Keywords:
antiviralschronic hepatitis Bgene editinghepatitis B virus

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Area of Science:

  • Hepatology and Virology
  • Drug Development and Delivery Systems

Background:

  • Chronic hepatitis B virus (HBV) infection is a major cause of cirrhosis and hepatocellular carcinoma.
  • Current nucleotide/nucleoside antiviral therapies suppress HBV replication but require lifelong daily adherence, which can be challenging for patients.

Purpose of the Study:

  • To review recent advances in long-acting formulations for HBV treatment and prevention.
  • To summarize novel compounds targeting the HBV life cycle and curative strategies.

Main Methods:

  • Review of current literature on long-acting antiviral formulations for HBV.
  • Summary of emerging compounds and genome editing technologies for HBV cure.

Main Results:

  • Long-acting formulations are being developed to potentially improve patient adherence to HBV therapy.
  • New compounds targeting distinct steps in the HBV life cycle are under investigation.
  • Curative strategies focus on eliminating covalently closed circular DNA and inactivating integrated viral DNA.

Conclusions:

  • Long-acting antivirals and genome editing present promising avenues for improved HBV management and potential cure.
  • These innovative approaches aim to overcome adherence challenges associated with current daily therapies.