HBV variants are common in the 'immune-tolerant' phase of chronic hepatitis B.


Journal

Journal of viral hepatitis
ISSN: 1365-2893
Titre abrégé: J Viral Hepat
Pays: England
ID NLM: 9435672

Informations de publication

Date de publication:
10 2020
Historique:
received: 08 01 2020
revised: 09 04 2020
accepted: 23 04 2020
pubmed: 10 5 2020
medline: 1 9 2021
entrez: 9 5 2020
Statut: ppublish

Résumé

Nucleos(t)ide analogues (NUC) treatment prevents progression of liver fibrosis in subjects with chronic hepatitis B (CHB). However, risk of hepatocellular carcinoma (HCC) persists despite viral suppression. Specific HBV variants have been associated with adverse outcomes, including HCC; however, the frequency of these variants during the seemingly benign immunotolerant (IT) phase is unknown. Next-generation sequencing and detailed virological characterization on a cohort of treatment-naïve IT subjects were performed to determine the frequency of clinically relevant viral variants. Samples from 97 subjects (genotype B/C 55%/45%, median HBV-DNA 8.5 log

Identifiants

pubmed: 32384174
doi: 10.1111/jvh.13318
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0
Hepatitis B Surface Antigens 0
Hepatitis B e Antigens 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1061-1070

Informations de copyright

© 2020 John Wiley & Sons Ltd.

Références

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Auteurs

Lilly Yuen (L)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Peter A Revill (PA)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
Department of Microbiology and Immunology, University of Melbourne, Parkville, Victoria, Australia.

Gillian Rosenberg (G)

National Cancer Research Institute, London, UK.

Josef Wagner (J)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Margaret Littlejohn (M)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Julianne Bayliss (J)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Kathy Jackson (K)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Susanna K Tan (SK)

Gilead Sciences, Inc, Foster City, CA, USA.

Anuj Gaggar (A)

Gilead Sciences, Inc, Foster City, CA, USA.

Kathryn Kitrinos (K)

Gilead Sciences, Inc, Foster City, CA, USA.

Mani Subramanian (M)

Gilead Sciences, Inc, Foster City, CA, USA.

Ed Gane (E)

New Zealand Transplant Unit, Auckland, New Zealand.

Henry L Y Chan (HLY)

Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong SAR.

Xin Li (X)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Scott Bowden (S)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Stephen Locarnini (S)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Alexander Thompson (A)

St Vincent's Hospital, Melbourne, Victoria, Australia.

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