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Article: Advances in determining new treatments for hepatitis B infection by utilizing existing and novel biomarkers

TitleAdvances in determining new treatments for hepatitis B infection by utilizing existing and novel biomarkers
Authors
Issue Date1-Mar-2023
PublisherTaylor and Francis Group
Citation
Expert Opinion on Drug Discovery, 2023, v. 18, n. 4, p. 1-16 How to Cite?
AbstractIntroduction: Chronic hepatitis B (CHB) infection is a major global health threat and accounts for significant liver-related morbidity and mortality. An improved understanding of how hepatitis B virus (HBV) interacts with the host immune system allows the discovery of novel biomarkers and new treatment options. Viral biomarkers including hepatitis B surface antigen (HBsAg) and newer ones like HBV RNA and hepatitis B core-related antigen appear to be useful to select patients who are likely to benefit from cessation of long-term antiviral therapy. These markers can also help to confirm target engagement for novel compounds, and efficacy in HBsAg reduction and seroclearance is deemed essential as this is how the current treatment endpoint of functional cure is defined. Areas covered: In this review, the authors discuss the current standard of care and the gaps between such standard and the ideal goals for treatment in CHB. The authors highlight novel viral and immunological biomarkers that are potentially useful to evaluate treatment response. Novel treatment approaches in relation to these novel biomarkers are also evaluated. Expert opinion: Novel serum viral biomarkers and immunological markers are indispensable in the HBV functional cure program. These will likely become part of standard monitoring soon.
Persistent Identifierhttp://hdl.handle.net/10722/328347
ISSN
2023 Impact Factor: 6.0
2023 SCImago Journal Rankings: 1.077
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMak, LY-
dc.contributor.authorHui, RWH-
dc.contributor.authorCheung, KS-
dc.contributor.authorFung, J-
dc.contributor.authorSeto, WK-
dc.contributor.authorYuen, MF-
dc.date.accessioned2023-06-28T04:42:51Z-
dc.date.available2023-06-28T04:42:51Z-
dc.date.issued2023-03-01-
dc.identifier.citationExpert Opinion on Drug Discovery, 2023, v. 18, n. 4, p. 1-16-
dc.identifier.issn1746-0441-
dc.identifier.urihttp://hdl.handle.net/10722/328347-
dc.description.abstractIntroduction: Chronic hepatitis B (CHB) infection is a major global health threat and accounts for significant liver-related morbidity and mortality. An improved understanding of how hepatitis B virus (HBV) interacts with the host immune system allows the discovery of novel biomarkers and new treatment options. Viral biomarkers including hepatitis B surface antigen (HBsAg) and newer ones like HBV RNA and hepatitis B core-related antigen appear to be useful to select patients who are likely to benefit from cessation of long-term antiviral therapy. These markers can also help to confirm target engagement for novel compounds, and efficacy in HBsAg reduction and seroclearance is deemed essential as this is how the current treatment endpoint of functional cure is defined. Areas covered: In this review, the authors discuss the current standard of care and the gaps between such standard and the ideal goals for treatment in CHB. The authors highlight novel viral and immunological biomarkers that are potentially useful to evaluate treatment response. Novel treatment approaches in relation to these novel biomarkers are also evaluated. Expert opinion: Novel serum viral biomarkers and immunological markers are indispensable in the HBV functional cure program. These will likely become part of standard monitoring soon.-
dc.languageeng-
dc.publisherTaylor and Francis Group-
dc.relation.ispartofExpert Opinion on Drug Discovery-
dc.titleAdvances in determining new treatments for hepatitis B infection by utilizing existing and novel biomarkers-
dc.typeArticle-
dc.identifier.doi10.1080/17460441.2023.2192920-
dc.identifier.hkuros344695-
dc.identifier.volume18-
dc.identifier.issue4-
dc.identifier.spage1-
dc.identifier.epage16-
dc.identifier.eissn1746-045X-
dc.identifier.isiWOS:000950965400001-
dc.identifier.issnl1746-0441-

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