The progress of molecules and strategies for the treatment of HBV infection

Front Cell Infect Microbiol. 2023 Mar 15:13:1128807. doi: 10.3389/fcimb.2023.1128807. eCollection 2023.

Abstract

Hepatitis B virus infections have always been associated with high levels of mortality. In 2019, hepatitis B virus (HBV)-related diseases resulted in approximately 555,000 deaths globally. In view of its high lethality, the treatment of HBV infections has always presented a huge challenge. The World Health Organization (WHO) came up with ambitious targets for the elimination of hepatitis B as a major public health threat by 2030. To accomplish this goal, one of the WHO's strategies is to develop curative treatments for HBV infections. Current treatments in a clinical setting included 1 year of pegylated interferon alpha (PEG-IFNα) and long-term nucleoside analogues (NAs). Although both treatments have demonstrated outstanding antiviral effects, it has been difficult to develop a cure for HBV. The reason for this is that covalently closed circular DNA (cccDNA), integrated HBV DNA, the high viral burden, and the impaired host immune responses all hinder the development of a cure for HBV. To overcome these problems, there are clinical trials on a number of antiviral molecules being carried out, all -showing promising results so far. In this review, we summarize the functions and mechanisms of action of various synthetic molecules, natural products, traditional Chinese herbal medicines, as clustered regularly interspaced short palindromic repeats and their associated proteins (CRISPR/Cas)-based systems, zinc finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), all of which could destroy the stability of the HBV life cycle. In addition, we discuss the functions of immune modulators, which can enhance or activate the host immune system, as well some representative natural products with anti-HBV effects.

Keywords: HBV; HBV life cycle; inhibitors; molecules; treatment.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / metabolism
  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use
  • DNA, Circular / metabolism
  • DNA, Circular / pharmacology
  • DNA, Circular / therapeutic use
  • DNA, Viral / genetics
  • Hepatitis B virus* / physiology
  • Hepatitis B* / drug therapy
  • Humans
  • Interferon-alpha / pharmacology
  • Virus Replication

Substances

  • Interferon-alpha
  • Antiviral Agents
  • DNA, Circular
  • DNA, Viral

Grants and funding

This research was supported by the Huadong Medicine-Joint Funds of the Zhejiang Provincial Natural Science Foundation of China under Grant No. LHDMD22H300001, Zhejiang Provincial Key Research & Development Plan (2021C03083).