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Related Concept Videos

Hepatitis01:25

Hepatitis

Hepatitis is an inflammatory condition of the liver most commonly caused by hepatotropic viruses (A–E), though non-infectious causes such as alcohol and drugs also exist.Hepatitis AHepatitis A virus (HAV) is a non-enveloped RNA virus of the Picornaviridae family. It is primarily transmitted via the fecal-oral route, typically through ingestion of contaminated food or water. After ingestion, HAV enters the bloodstream through the oropharynx or intestinal epithelium and reaches the liver. The...
Viral Hepatitis I: Introduction01:28

Viral Hepatitis I: Introduction

Viral hepatitis is an inflammatory condition of the liver caused by infection with hepatotropic viruses, most commonly hepatitis A, B, C, D, and E. Despite variations in structure and transmission, all viruses mentioned infect hepatocytes and provoke immune responses that can hinder liver function. Additionally, some non-hepatotropic viruses can also lead to hepatic inflammation.Hepatitis A VirusHepatitis A virus (HAV) is transmitted through the fecal–oral route, typically by ingestion of food...
Inhibitors of Viral Protein Synthesis01:30

Inhibitors of Viral Protein Synthesis

Protein synthesis is indispensable for viral replication, as viruses lack the cellular machinery required for this process and must hijack the host's translational apparatus. In response, host cells deploy a critical innate immune defense involving interferons, specialized cytokines that play a central role in inhibiting viral propagation.Upon viral detection, infected cells release interferons that bind to receptors on adjacent uninfected cells, activating the JAK-STAT signaling pathway and...
Retrovirus Life Cycles01:10

Retrovirus Life Cycles

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 retrovirus to...

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Meta-analysis: antiviral treatment for hepatitis D.

C Triantos1, M Kalafateli, V Nikolopoulou

  • 1Department of Gastroenterology, University Hospital of Patras, Stamatopoulou 4, Patras, Greece. chtriantos@hotmail.com

Alimentary Pharmacology & Therapeutics
|January 26, 2012
PubMed
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Hepatitis D (HDV) treatment remains challenging. Pegylated interferon alfa (PEG-IFNa) shows superiority over other medications for viral clearance and sustained response, suggesting its potential in future combination therapies.

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Area of Science:

  • Hepatology
  • Virology
  • Clinical Pharmacology

Background:

  • Hepatitis D virus (HDV) infection lacks effective therapeutic options.
  • Current treatments for HDV are unsatisfactory, necessitating further research.

Purpose of the Study:

  • To conduct a meta-analysis evaluating the efficacy of various treatments for Hepatitis D.
  • To compare different interferon-based therapies for HDV infection.

Main Methods:

  • Systematic literature search of Medline, Scopus, Cochrane Library, and ISI Web of Knowledge.
  • Inclusion of randomized clinical trials (RCTs) comparing interferon alfa (IFNa), pegylated interferon alfa (PEG-IFNa), and combination therapies.
  • Endpoints included biochemical and virological response at end of treatment (EOT) and end of follow-up (EOFUP), histological improvement, and HDAg clearance.

Main Results:

  • Interferon alfa (IFNa) demonstrated efficacy for end-of-treatment (EOT) biochemical and virological response but not sustained response.
  • High-dose IFNa was superior to low-dose IFNa for EOT outcomes.
  • Pegylated interferon alfa (PEG-IFNa) showed significant advantages in EOT virological response, EOFUP virological response, and necroinflammatory activity improvement compared to other medications.

Conclusions:

  • Long-term suppression of HDV RNA by IFNa is not consistently maintained.
  • Adding lamivudine to IFNa did not show significant benefits.
  • PEG-IFNa is a more effective treatment option for HDV infection, outperforming other medications in achieving virological response and sustained viral suppression.