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Articles Published Processes
4/25/2025 8:23:04 AM | Browse: 2 | Download: 0
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Received |
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2025-02-08 06:41 |
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Peer-Review Started |
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2025-02-08 06:41 |
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To Make the First Decision |
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Return for Revision |
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2025-03-10 02:44 |
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Revised |
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2025-03-21 09:05 |
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Second Decision |
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2025-04-09 02:40 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2025-04-09 08:50 |
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Articles in Press |
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2025-04-09 08:50 |
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Publication Fee Transferred |
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2025-03-24 07:05 |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2025-04-18 01:05 |
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Publish the Manuscript Online |
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2025-04-25 08:23 |
ISSN |
1948-5182 (online) |
Open Access |
This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
Copyright |
© The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved. |
Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
Website |
http://www.wjgnet.com |
Category |
Infectious Diseases |
Manuscript Type |
Minireviews |
Article Title |
Drug development for chronic hepatitis B functional cure: Recent progress
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Manuscript Source |
Unsolicited Manuscript |
All Author List |
Ting Liu, He Wang, Yue Zhao, Ying-Xin Wang, Xue Xing and Peng Gao |
ORCID |
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Funding Agency and Grant Number |
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Corresponding Author |
Peng Gao, PhD, Professor, Department of Clinical Laboratory, The Second Affiliated Hospital of Dalian Medical University, No. 467 Zhongshan Road, Dalian 116021, Liaoning Province, China. gaop@dmu.edu.cn |
Key Words |
Chronic hepatitis B infection; Therapeutic targets; Monoclonal antibody; RNA interference; Immunomodulators |
Core Tip |
As we know, chronic hepatitis B virus (HBV) infection can lead to liver failure and cirrhosis, resulting in significantly increased morbidity and mortality rates. Current antiviral nucleos(t)ide analogues suppress HBV replication but are limited in reducing hepatitis B surface antigen (HBsAg) levels. Interferon alpha, an immunomodulator, is restricted by safety concerns and adverse reactions. New drug development aims for a functional cure, defined as HBsAg clearance and sustained HBV DNA suppression. This review highlights recent advancements in novel therapies targeting HBV, including HBsAg entry inhibitors, monoclonal antibodies, transcription inhibitors, and immunomodulatory agents like TLR-7/8 agonists, immune checkpoint inhibitors, and therapeutic vaccines. |
Publish Date |
2025-04-25 08:23 |
Citation |
<p>Liu T, Wang H, Zhao Y, Wang YX, Xing X, Gao P. Drug development for chronic hepatitis B functional cure: Recent progress. <i>World J Hepatol</i> 2025; 17(4): 105797</p> |
URL |
https://www.wjgnet.com/1948-5182/full/v17/i4/105797.htm |
DOI |
https://dx.doi.org/10.4254/wjh.v17.i4.105797 |
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