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Review
. 2025 Apr 11;26(8):3633.
doi: 10.3390/ijms26083633.

Functional Cure for Hepatitis B Virus: Challenges and Achievements

Affiliations
Review

Functional Cure for Hepatitis B Virus: Challenges and Achievements

Oren Shechter et al. Int J Mol Sci. .

Abstract

The Hepatitis B Virus (HBV) presents a formidable global health challenge, impacting hundreds of millions worldwide and imposing a considerable burden on healthcare systems. The elusive nature of the virus, with its ability to establish chronic infection and evade immune detection, and the absence of curative agents have prompted efforts to develop novel therapeutic approaches beyond current antiviral treatments. This review addresses the challenging concept of a functional cure for HBV, a state characterized by the suppression of HBV and HBsAg, mitigating disease progression and transmission without a complete cure. We provide an overview of HBV epidemiology and its clinical impact, followed by an exploration of the current treatment landscape and its limitations. The immunological basis of a functional cure is then discussed, exploring the intricate interplay between the virus and the host immune response. Emerging therapeutic approaches, such as RNA interference-based interventions, entry inhibitors, nucleic acid polymers, and therapeutic vaccines, are discussed with regard to their success in achieving a functional cure. Lastly, the review underscores the urgent need for innovative strategies to achieve a functional cure for HBV.

Keywords: HBsAg; PEG-IFNα therapy; functional cure; hepatitis B virus (HBV); immunological markers; nucleos(t)ide analog (NA) therapy; siRNA therapy; therapeutic vaccine.

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Conflict of interest statement

Author Andrew Vaillant was employed by the company Replicor Inc. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

    1. Magnius L., Mason W.S., Taylor J., Kann M., Glebe D., Deny P., Sureau C., Norder H., ICTV Report Consortium ICTV Virus Taxonomy Profile: Hepadnaviridae. J. Gen. Virol. 2020;101:571–572. doi: 10.1099/jgv.0.001415. - DOI - PMC - PubMed
    1. Rizzo G.E.M., Cabibbo G., Craxi A. Hepatitis B Virus-Associated Hepatocellular Carcinoma. Viruses. 2022;14:986. doi: 10.3390/v14050986. - DOI - PMC - PubMed
    1. WHO Organization Hepatitis B. [(accessed on 15 December 2024)]. Available online: https://www.who.int/news-room/fact-sheets/detail/hepatitis-b.
    1. Easterbrook P.J., Luhmann N., Bajis S., Min M.S., Newman M., Lesi O., Doherty M.C. WHO 2024 hepatitis B guidelines: An opportunity to transform care. Lancet Gastroenterol. Hepatol. 2024;9:493–495. doi: 10.1016/S2468-1253(24)00089-X. - DOI - PubMed
    1. Xia Y., Guo H. Hepatitis B virus cccDNA: Formation, regulation and therapeutic potential. Antivir. Res. 2020;180:104824. doi: 10.1016/j.antiviral.2020.104824. - DOI - PMC - PubMed

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