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Retrovirus Life Cycles01:10

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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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Related Experiment Video

Updated: May 30, 2025

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Decrease in HBsAg After TAF Switching from Entecavir During Long-Term Treatment of Chronic Hepatitis B Virus

Kazuto Tajiri1, Yuka Hayashi1, Aiko Murayama1

  • 1Third Department of Internal Medicine, Faculty of Medicine, Academic Assembly, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.

Viruses
|January 25, 2025
PubMed
Summary

Switching to tenofovir alafenamide fumarate (TAF) may decrease hepatitis B surface antigen (HBsAg) in some chronic hepatitis B patients, especially those with lower baseline HBsAg levels and mild fibrosis. TAF was well-tolerated in this study.

Keywords:
HBsAg decreasedyslipidemiahepatitis B virusnucleos(t)ide analogue switchingtenofovir alafenamide fumarate

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Area of Science:

  • Hepatology
  • Virology
  • Pharmacology

Background:

  • Hepatitis B virus (HBV) infection is a global health concern.
  • Nucleos(t)ide analogues (NAs) are standard treatment for chronic hepatitis B (CHB).
  • Achieving HBsAg seroclearance remains a challenge in CHB management.

Purpose of the Study:

  • To evaluate the effect of switching from entecavir (ETV) to tenofovir alafenamide fumarate (TAF) on HBsAg levels in CHB patients.
  • To assess the safety and tolerability of TAF in this patient population.
  • To identify factors associated with HBsAg reduction after switching to TAF.

Main Methods:

  • Retrospective study of 77 CHB patients.
  • 47 patients switched from ETV to TAF.
  • Median follow-up of 40 months post-switch; median 60 months HBsAg monitoring pre-switch.

Main Results:

  • No significant overall change in HBsAg levels post-switch.
  • Significant HBsAg decrease observed in patients with baseline HBsAg < 100 IU/mL.
  • HBsAg loss occurred in three patients switching to TAF.
  • TAF was well-tolerated with no adverse effects.
  • Higher Fib-4 index (liver fibrosis marker) at switch was associated with decreased HBsAg.

Conclusions:

  • Switching from ETV to TAF can be an effective strategy for managing CHB.
  • Hepatic inflammation, indicated by Fib-4 index, may play a role in HBsAg reduction.
  • Patients with mild to moderate fibrosis may benefit more from TAF regarding HBsAg reduction.