Long term effect of alpha interferon in children with chronic hepatitis B

F Bortolotti1, P Jara, C Barbera

  • 1Clinica Medica 5, University of Padua, Italy.

Gut
|April 15, 2000
PubMed

Insights

Interferon alpha (IFN) treatment for chronic hepatitis B in children did not improve long-term HBeAg clearance rates compared to controls. However, IFN accelerated HBsAg loss in patients with active disease who responded early.

Area of Science:

  • Pediatric Hepatology
  • Viral Hepatitis Research
  • Immunomodulatory Therapy

Background:

  • Chronic hepatitis B (CHB) infection in children requires long-term management and prognosis assessment.
  • Interferon (IFN) alpha has been used to treat CHB, but its long-term impact on disease progression in pediatric populations needs further definition.

Purpose of the Study:

  • To define the long-term prognosis of chronic hepatitis B infection in children treated with interferon alpha.
  • To evaluate the sustained efficacy of IFN alpha in pediatric CHB patients.

Main Methods:

  • A cohort of 107 children with CHB received IFN alpha for 3-6 months and were followed for a mean of 69 months.
  • Treatment response was defined by hepatitis B e antigen (HBeAg) loss within 12 months post-treatment.
  • A control group of 59 untreated children was followed for a mean of 46 months.

Main Results:

  • Sustained HBeAg clearance rates at five years were similar between IFN-treated children (60%) and controls (65%).
  • High baseline transaminases and histological activity index predicted treatment response.
  • Hepatitis B surface antigen (HBsAg) loss occurred in 25% of early responders treated with IFN, but not in non-responders or controls.

Conclusions:

  • IFN alpha treatment in children with CHB appears to accelerate spontaneous HBeAg clearance rather than increase the overall rate.
  • IFN alpha significantly enhanced HBsAg loss in children with active disease who responded early, suggesting a specific benefit for this subgroup.
Abstract

Related Concept Videos

Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow01:26

Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow

Chronic liver disease significantly impacts drug metabolism due to alterations in hepatic blood flow and enzyme accessibility. This disruption affects the body's pharmacokinetics—the movement and processing of drugs within the system. Key enzymes crucial for metabolizing medications become less accessible, changing how drugs are processed and utilized. Furthermore, liver disease influences the synthesis of plasma proteins, such as albumin and globulins, which play critical roles in drug binding...
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test01:22

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test

In clinical practice, the direct measurement of hepatic blood flow to evaluate liver function presents significant challenges due to the intricate and specialized nature of the necessary techniques. Consequently, healthcare professionals often rely on empirical estimates derived from thorough patient examinations and liver function tests to gauge liver health. Among the tools at their disposal, the Child–Pugh and MELD scoring systems stand out for their ability to categorize and assess the...
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment01:08

Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment

Hepatic impairment, characterized by decreased liver function, does not uniformly mandate adjustments in drug dosage. Whether dosage modifications are necessary depends on various factors related to the drug's metabolism and elimination pathways. If a drug is primarily excreted via the kidneys and bypasses significant hepatic processing, if it undergoes minimal metabolic transformation in the liver, or if it is volatile and primarily expelled through the lungs, dose adjustments may not be...
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...
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...
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...