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Article: Novel developments of hepatitis B: treatment goals, agents and monitoring tools

TitleNovel developments of hepatitis B: treatment goals, agents and monitoring tools
Authors
KeywordsAntiviral therapy
cirrhosis
core protein allosteric modulator
covalently closed circular DNA
cure
genome editing
global elimination
HBV RNA
hepatitis B core-related antigen
hepatitis B virus
hepatocellular carcinoma
immunomodulator
integrated DNA
prevention
programmed cell death protein 1
RNA interfering gene silencer
therapeutic vaccine
vaccination
viral entry inhibitor
Issue Date2019
PublisherTaylor & Francis. The Journal's web site is located at http://www.tandfonline.com/loi/ierj20#.VgGhakaFOnI
Citation
Expert Review of Clinical Pharmacology, 2019, v. 12 n. 2, p. 109-120 How to Cite?
AbstractIntroduction: Chronic hepatitis B (CHB) infection causes considerable morbidity and mortality and hence should be a target for global elimination. In recent years, advances have been made in understanding the disease pathophysiology and the relationship to clinical outcome. Novel treatment targets are actively being sought in the hope of improving the treatment outlook. Areas covered: We discussed the cascade of cure of CHB with respect to the degree of persistence of viral genome and proteins. Several novel antiviral agents either targeting the virus or the host are in different clinical phases of development. Serum hepatitis B core-related antigen and HBV RNA are novel markers, which might have a role in the prediction of specific clinical outcomes such as development of hepatocellular carcinoma or virological relapse after cessation of antiviral therapy. These markers may also be used to monitor treatment response in the drug trials. Expert commentary: Global elimination of CHB is challenged by extremely low awareness of illness and poor access to care. CHB and its related complications can be reduced by birth dose vaccine, antiviral therapy, and alleviated by complication screening. Treatment options for CHB will expand in the next decade and early functional cure is not an impractical goal.
Persistent Identifierhttp://hdl.handle.net/10722/267450
ISSN
2023 Impact Factor: 3.6
2023 SCImago Journal Rankings: 0.990
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMak, LY-
dc.contributor.authorSeto, WKW-
dc.contributor.authorFung, JYY-
dc.contributor.authorYuen, RMF-
dc.date.accessioned2019-02-18T09:02:18Z-
dc.date.available2019-02-18T09:02:18Z-
dc.date.issued2019-
dc.identifier.citationExpert Review of Clinical Pharmacology, 2019, v. 12 n. 2, p. 109-120-
dc.identifier.issn1751-2433-
dc.identifier.urihttp://hdl.handle.net/10722/267450-
dc.description.abstractIntroduction: Chronic hepatitis B (CHB) infection causes considerable morbidity and mortality and hence should be a target for global elimination. In recent years, advances have been made in understanding the disease pathophysiology and the relationship to clinical outcome. Novel treatment targets are actively being sought in the hope of improving the treatment outlook. Areas covered: We discussed the cascade of cure of CHB with respect to the degree of persistence of viral genome and proteins. Several novel antiviral agents either targeting the virus or the host are in different clinical phases of development. Serum hepatitis B core-related antigen and HBV RNA are novel markers, which might have a role in the prediction of specific clinical outcomes such as development of hepatocellular carcinoma or virological relapse after cessation of antiviral therapy. These markers may also be used to monitor treatment response in the drug trials. Expert commentary: Global elimination of CHB is challenged by extremely low awareness of illness and poor access to care. CHB and its related complications can be reduced by birth dose vaccine, antiviral therapy, and alleviated by complication screening. Treatment options for CHB will expand in the next decade and early functional cure is not an impractical goal.-
dc.languageeng-
dc.publisherTaylor & Francis. The Journal's web site is located at http://www.tandfonline.com/loi/ierj20#.VgGhakaFOnI-
dc.relation.ispartofExpert Review of Clinical Pharmacology-
dc.rightsThis is an electronic version of an article published in [include the complete citation information for the final version of the article as published in the print edition of the journal]. [JOURNAL TITLE] is available online at: http://www.informaworld.com/smpp/ with the open URL of your article.-
dc.subjectAntiviral therapy-
dc.subjectcirrhosis-
dc.subjectcore protein allosteric modulator-
dc.subjectcovalently closed circular DNA-
dc.subjectcure-
dc.subjectgenome editing-
dc.subjectglobal elimination-
dc.subjectHBV RNA-
dc.subjecthepatitis B core-related antigen-
dc.subjecthepatitis B virus-
dc.subjecthepatocellular carcinoma-
dc.subjectimmunomodulator-
dc.subjectintegrated DNA-
dc.subjectprevention-
dc.subjectprogrammed cell death protein 1-
dc.subjectRNA interfering gene silencer-
dc.subjecttherapeutic vaccine-
dc.subjectvaccination-
dc.subjectviral entry inhibitor-
dc.titleNovel developments of hepatitis B: treatment goals, agents and monitoring tools-
dc.typeArticle-
dc.identifier.emailSeto, WKW: wkseto@hku.hk-
dc.identifier.emailFung, JYY: jfung@hkucc.hku.hk-
dc.identifier.emailYuen, RMF: mfyuen@hku.hk-
dc.identifier.authoritySeto, WKW=rp01659-
dc.identifier.authorityFung, JYY=rp00518-
dc.identifier.authorityYuen, RMF=rp00479-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1080/17512433.2019.1567327-
dc.identifier.pmid30621472-
dc.identifier.scopuseid_2-s2.0-85060928844-
dc.identifier.hkuros296778-
dc.identifier.volume12-
dc.identifier.issue2-
dc.identifier.spage109-
dc.identifier.epage120-
dc.identifier.isiWOS:000457422900006-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl1751-2433-

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