File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.3350/cmh.2024.0855
- Scopus: eid_2-s2.0-86000775619
- PMID: 39541952
- WOS: WOS:001468597800008
- Find via

Supplementary
- Citations:
- Appears in Collections:
Article: Prospect of emerging treatments for hepatitis B virus functional cure
| Title | Prospect of emerging treatments for hepatitis B virus functional cure |
|---|---|
| Authors | |
| Keywords | Antiviral agents Chronic hepatitis B Hepatitis B surface antigen Hepatitis B virus Interferons |
| Issue Date | 1-Feb-2025 |
| Publisher | Korean 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 Identifier | http://hdl.handle.net/10722/357959 |
| ISSN | 2023 Impact Factor: 14.0 2023 SCImago Journal Rankings: 3.128 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Hui, Rex Wan Hin | - |
| dc.contributor.author | Mak, Lung Yi | - |
| dc.contributor.author | Fung, James | - |
| dc.contributor.author | Seto, Wai Kay | - |
| dc.contributor.author | Yuen, Man Fung | - |
| dc.date.accessioned | 2025-07-23T00:30:58Z | - |
| dc.date.available | 2025-07-23T00:30:58Z | - |
| dc.date.issued | 2025-02-01 | - |
| dc.identifier.citation | Clinical and Molecular Hepatology, 2025, v. 31, p. S165-S181 | - |
| dc.identifier.issn | 2287-2728 | - |
| dc.identifier.uri | http://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.language | eng | - |
| dc.publisher | Korean Association for the Study of the Liver | - |
| dc.relation.ispartof | Clinical and Molecular Hepatology | - |
| dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
| dc.subject | Antiviral agents | - |
| dc.subject | Chronic hepatitis B | - |
| dc.subject | Hepatitis B surface antigen | - |
| dc.subject | Hepatitis B virus | - |
| dc.subject | Interferons | - |
| dc.title | Prospect of emerging treatments for hepatitis B virus functional cure | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.3350/cmh.2024.0855 | - |
| dc.identifier.pmid | 39541952 | - |
| dc.identifier.scopus | eid_2-s2.0-86000775619 | - |
| dc.identifier.volume | 31 | - |
| dc.identifier.spage | S165 | - |
| dc.identifier.epage | S181 | - |
| dc.identifier.eissn | 2287-285X | - |
| dc.identifier.isi | WOS:001468597800008 | - |
| dc.identifier.issnl | 2287-2728 | - |
