Chronic hepatitis B: the demise of the 'inactive carrier' phase

Apostolos Koffas1, Manoj Kumar2, Upkar S Gill3

  • 1Department of Gastroenterology, General University Hospital of Larisa, Larisa, Greece.

Hepatology International
|February 27, 2021
PubMed

Insights

The term "inactive carrier" for chronic hepatitis B (CHB) is outdated and misleading. New research suggests a "Treat All" approach may be beneficial for HBeAg-negative CHB patients to prevent liver disease progression and hepatocellular carcinoma (HCC).

Area of Science:

  • Hepatology
  • Virology
  • Immunology

Background:

  • Chronic hepatitis B (CHB) continues to pose a significant global health challenge, with liver cirrhosis and hepatocellular carcinoma (HCC) remaining major concerns.
  • Recent advancements in understanding CHB immunopathogenesis have prompted revisions in clinical classifications, moving away from the term 'inactive carrier'.

Purpose of the Study:

  • To review current literature and guidelines regarding hepatitis B e antigen (HBeAg)-negative chronic infection.
  • To advocate for the abandonment of the term 'inactive carrier' due to its potential to underestimate disease activity and risks.
  • To discuss the implications of new HBV therapies and consider a 'Treat All' approach.

Main Methods:

  • Literature review of current guidelines and research on CHB.
  • Analysis of clinical classifications and terminology used by EASL and APASL.
  • Evaluation of treatment thresholds and endpoints, including HBsAg loss.

Main Results:

  • The 'inactive carrier' state is a misnomer, as CHB patients may still have underlying liver disease and a risk of reactivation or progression.
  • New terms like 'HBeAg-negative chronic infection' and 'Incidentally Detected Asymptomatic Hepatitis B surface antigen (HBsAg)-positive Subject (IDAHS)' offer more accurate descriptions.
  • Hepatocellular carcinoma (HCC) development and spontaneous reactivation risks are not negligible even in HBeAg-negative CHB.

Conclusions:

  • The term 'inactive carrier' should be abandoned in favor of more accurate terminology.
  • Lowering treatment thresholds and adopting a 'Treat All' strategy should be considered, especially with emerging therapies.
  • HBsAg loss is an achievable and optimal treatment endpoint for CHB, including HBeAg-negative stages.

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