File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Prospect of emerging treatments for hepatitis B virus functional cure

TitleProspect of emerging treatments for hepatitis B virus functional cure
Authors
KeywordsAntiviral agents
Chronic hepatitis B
Hepatitis B surface antigen
Hepatitis B virus
Interferons
Issue Date1-Feb-2025
PublisherKorean Association for the Study of the Liver
Citation
Clinical and Molecular Hepatology, 2025, v. 31, p. S165-S181 How to Cite?
Abstract

Functional cure, defined as sustained hepatitis B surface antigen (HBsAg) seroclearance with unquantifiable hepatitis B virus (HBV) DNA at 24 weeks off treatment, is a favorable treatment endpoint in chronic hepatitis B (CHB). Nonetheless, functional cure is rarely attained with the current treatment modalities of nucleos(t)ide analogues (NUCs) and pegylated interferon alpha. Multiple novel virus-targeting agents and immunomodulators are under development for HBV with functional cure as the treatment goal. Among virus-targeting agents, antisense oligonucleotides and small-interfering RNAs are the most advanced in the developmental pipeline, and can induce potent and sustainable HBsAg suppression. The other virus-targeting agents have varying effects on HBsAg and HBV DNA, depending on the drug mechanism. In contrast, immunomodulators have modest effects on HBsAg and have limited roles in monotherapy. Multiple combination regimens incorporating RNA interference agents with immunomodulators have been studied through many ongoing clinical trials. These combination strategies demonstrate synergistic effects in inducing functional cure, and will likely be the future direction of development. Despite the promising results, research is warranted to optimize treatment protocols and to establish criteria for NUC withdrawal after novel therapies. Functional cure is now an attainable target in CHB, and the emerging novel therapeutics will revolutionize CHB management.


Persistent Identifierhttp://hdl.handle.net/10722/357959
ISSN
2023 Impact Factor: 14.0
2023 SCImago Journal Rankings: 3.128
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHui, Rex Wan Hin-
dc.contributor.authorMak, Lung Yi-
dc.contributor.authorFung, James-
dc.contributor.authorSeto, Wai Kay-
dc.contributor.authorYuen, Man Fung-
dc.date.accessioned2025-07-23T00:30:58Z-
dc.date.available2025-07-23T00:30:58Z-
dc.date.issued2025-02-01-
dc.identifier.citationClinical and Molecular Hepatology, 2025, v. 31, p. S165-S181-
dc.identifier.issn2287-2728-
dc.identifier.urihttp://hdl.handle.net/10722/357959-
dc.description.abstract<p>Functional cure, defined as sustained hepatitis B surface antigen (HBsAg) seroclearance with unquantifiable hepatitis B virus (HBV) DNA at 24 weeks off treatment, is a favorable treatment endpoint in chronic hepatitis B (CHB). Nonetheless, functional cure is rarely attained with the current treatment modalities of nucleos(t)ide analogues (NUCs) and pegylated interferon alpha. Multiple novel virus-targeting agents and immunomodulators are under development for HBV with functional cure as the treatment goal. Among virus-targeting agents, antisense oligonucleotides and small-interfering RNAs are the most advanced in the developmental pipeline, and can induce potent and sustainable HBsAg suppression. The other virus-targeting agents have varying effects on HBsAg and HBV DNA, depending on the drug mechanism. In contrast, immunomodulators have modest effects on HBsAg and have limited roles in monotherapy. Multiple combination regimens incorporating RNA interference agents with immunomodulators have been studied through many ongoing clinical trials. These combination strategies demonstrate synergistic effects in inducing functional cure, and will likely be the future direction of development. Despite the promising results, research is warranted to optimize treatment protocols and to establish criteria for NUC withdrawal after novel therapies. Functional cure is now an attainable target in CHB, and the emerging novel therapeutics will revolutionize CHB management.</p>-
dc.languageeng-
dc.publisherKorean Association for the Study of the Liver-
dc.relation.ispartofClinical and Molecular Hepatology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAntiviral agents-
dc.subjectChronic hepatitis B-
dc.subjectHepatitis B surface antigen-
dc.subjectHepatitis B virus-
dc.subjectInterferons-
dc.titleProspect of emerging treatments for hepatitis B virus functional cure -
dc.typeArticle-
dc.identifier.doi10.3350/cmh.2024.0855-
dc.identifier.pmid39541952-
dc.identifier.scopuseid_2-s2.0-86000775619-
dc.identifier.volume31-
dc.identifier.spageS165-
dc.identifier.epageS181-
dc.identifier.eissn2287-285X-
dc.identifier.isiWOS:001468597800008-
dc.identifier.issnl2287-2728-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats