The Role of Hepatitis B Core-Related Antigen.


Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
09 05 2019
Historique:
received: 02 04 2019
revised: 02 05 2019
accepted: 06 05 2019
entrez: 12 5 2019
pubmed: 12 5 2019
medline: 12 5 2019
Statut: epublish

Résumé

Hepatitis B virus (HBV) cannot be completely eliminated from infected hepatocytes due to the existence of intrahepatic covalently closed circular DNA (cccDNA). Serological biomarkers reflect intrahepatic viral replicative activity as non-invasive alternatives to liver biopsy. Hepatitis B core-related antigen (HBcrAg) is a novel biomarker that has an important role in chronic hepatitis B (CHB), because it correlates with serum HBV DNA and intrahepatic cccDNA. In clinical cases with undetectable serum HBV DNA or loss of HBsAg, HBcrAg still can be detected and the decrease in HBcrAg levels is significantly associated with promising outcomes for CHB patients. HBcrAg can predict spontaneous or treatment-induced hepatitis B envelope antigen (HBeAg) seroconversion, persistent responses before and after cessation of nucleos(t)ide analogues, potential HBV reactivation, HBV reinfection after liver transplantation, and risk of hepatocellular carcinoma progression or recurrence. In this review, the clinical applications of HBcrAg in CHB patients based on its virological features are described. Furthermore, new potential therapeutic anti-HBV agents that affect intrahepatic cccDNA are under development, and the monitoring of HBcrAg might be useful to judge therapeutic effects. In conclusion, HBcrAg might be a suitable surrogate marker beyond other HBV markers to predict the disease progression and treatment responses of CHB patients.

Identifiants

pubmed: 31075974
pii: genes10050357
doi: 10.3390/genes10050357
pmc: PMC6562807
pii:
doi:

Substances chimiques

Antiviral Agents 0
Biomarkers 0
Hepatitis B Core Antigens 0
Hepatitis B e Antigens 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Déclaration de conflit d'intérêts

Funding: This research was supported by AMED under Grant Number JP19fk0310101h0003.

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Auteurs

Takako Inoue (T)

Department of Clinical Laboratory Medicine, Nagoya City University Hospital, Nagoya 467-8602, Japan. clinoue@med.nagoya-cu.ac.jp.

Yasuhito Tanaka (Y)

Department of Clinical Laboratory Medicine, Nagoya City University Hospital, Nagoya 467-8602, Japan. ytanaka@med.nagoya-cu.ac.jp.
Department of Virology and Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan. ytanaka@med.nagoya-cu.ac.jp.

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Classifications MeSH