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Early Treatment Consideration in Patients with Hepatitis B ‘e’ Antigen-Positive Chronic Infection: Is It Time for a Paradigm Shift?

Apostolos Koffas, +3 more
- 26 Apr 2022 - 
- Vol. 14, Iss: 5, pp 900-900
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TLDR
The current review discusses the reasons to consider early antiviral therapy in HBeAg-positive chronic infection, and suggests lowering the treatment threshold to broaden treatment eligibility is likely to slow disease progression and reduce the risk of developing HCC.
Abstract
Chronic hepatitis B (CHB) is associated with significant morbidity and mortality, due to the adverse sequelae of cirrhosis and hepatocellular carcinoma (HCC). To date, antiviral therapy has been reserved for patients with ostensibly active liver disease, fibrosis or cirrhosis, and/or increased risk of HCC. Historically, patients with hepatitis B ‘e’ antigen (HBeAg)-positive chronic infection, were not offered antiviral therapy. Nevertheless, there has been compelling evidence emerging in recent years, demonstrating that this disease phase is in fact not characterized by immunological tolerance. HBV integration into the human genome is a frequent event found in these patients. Additionally, it may well be associated with active inflammation and fibrosis, even in the presence of persistently normal liver enzymes. Likewise, it appears that the mechanisms of hepatocarcinogenesis are already present during this early stage of the disease. This was reflected in the European Association for the Study of the Liver (EASL) guidelines, where treating patients above the age of 30 years with HBeAg-positive chronic infection was proposed. Lowering the treatment threshold to broaden treatment eligibility is likely to slow disease progression and reduce the risk of developing HCC. The current review discusses the reasons to consider early antiviral therapy in HBeAg-positive chronic infection.

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Citations
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Journal ArticleDOI

IFIT3 Is Increased in Serum from Patients with Chronic Hepatitis B Virus (HBV) Infection and Promotes the Anti-HBV Effect of Interferon Alpha via JAK-STAT2 In Vitro

TL;DR: In this article , the effect of IFIT3 on the Janus kinase-signal transducer and activator of transcription (JAK-STAT) signaling pathway under the dual intervention of IFN-α and HBV was also explored in vitro.
Journal ArticleDOI

Hepatitis B and D: an overview of the diagnosis and management

Apostolos Koffas, +1 more
- 01 Mar 2023 - 
TL;DR: In this paper , the authors proposed bulevirtide, a first-in-class entry inhibitor, for chronic hepatitis B (CHB) treatment, which is the most aggressive form of viral hepatitis.
References
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Journal ArticleDOI

EASL 2017 Clinical Practice Guidelines on the management of hepatitis B virus infection.

TL;DR: This Clinical Practice Guideline presents updated recommendations for the optimal management of HBV infection, and future treatment strategies to achieve 'cure' of disease and new biomarkers are discussed.
Journal ArticleDOI

Risk of hepatocellular carcinoma across a biological gradient of serum hepatitis B virus DNA level.

TL;DR: Elevated serum HBV DNA level (> or =10,000 copies/mL) is a strong risk predictor of hepatocellular carcinoma independent of HBeAg, serum alanine aminotransferase level, and liver cirrhosis.
Journal ArticleDOI

Characterization of hepatitis B virus (HBV)-specific T-cell dysfunction in chronic HBV infection.

TL;DR: A broad spectrum of anti-HBV immunity is expressed by patients with chronic HBV infection and this spectrum is proportional to HBV replication levels and can be improved by blocking the PD-1/PD-L1 pathway.
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