Abstract |
Functional cure, as defined by seroclearance of hepatitis B surface antigen ( HBsAg), is the desired treatment endpoint for chronic hepatitis B (CHB) infection, yet is rarely achieved with the currently approved therapy. Novel treatments currently in the clinical phase of development act by inhibiting viral replication/ antigen reduction and/or by restoring host immune control. Although some agents are effective in reducing the viral antigen load, a greater magnitude of suppression is required to achieve functional cure. Compounds that target the covalently closed circular DNA (cccDNA) pool, hepatitis B X (HBx) protein inhibition, and mRNA destabilization are also in the preclinical phase of development. Challenges which remain include the clinical implications, immunological perturbations, and safety of these novel compounds to be used in the real-life setting.
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Authors | Lung-Yi Mak, Ka-Shing Cheung, James Fung, Wai-Kay Seto, Man-Fung Yuen |
Journal | Trends in molecular medicine
(Trends Mol Med)
Vol. 28
Issue 9
Pg. 742-757
(09 2022)
ISSN: 1471-499X [Electronic] England |
PMID | 35780008
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2022 Elsevier Ltd. All rights reserved. |
Chemical References |
- Antiviral Agents
- DNA, Viral
- Hepatitis B Surface Antigens
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Topics |
- Antiviral Agents
- DNA, Viral
- Hepatitis B Surface Antigens
- Hepatitis B virus
- Hepatitis B, Chronic
- Humans
- Virus Replication
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