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Updated: Aug 19, 2025

Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix
Published on: October 20, 2021
Antimicrobial peptides: natural or synthetic defense peptides against HBV and HCV infections
Masoud Keikha1,2, Hossein Kamali3, Kiarash Ghazvini1,2
1Department of Microbiology and Virology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Abstract:
According to the literature, treatment of HCV and HBV infections faces challenges due to problems such as the emergence of drug-resistant mutants, the high cost of treatment, and the side effects of current antiviral therapy. Antimicrobial peptides (AMPs), a group of small peptides, are a part of the immune system and are considered as an alternative treatment for microbial infections. These peptides are water-soluble with amphiphilic (hydrophilic and hydrophobic surfaces) characteristics. AMPs are produced by a wide range of organisms including both prokaryotic and eukaryotic cells. The antiviral mechanisms of AMPs include inhibiting virus entry, inhibiting intracellular virus replication, inhibiting intracellular viral packaging, and inducing immune responses. In addition, AMPs are a new generation of antiviral biomolecules that have very low toxicity for human host cells, particularly liver cell lines. AMPs can be considered as one of the most important strategies for developing new adjuvant drugs in the treatment of HBV and HCV infections. In the present study, several groups of AMPs (with a net positive charge) such as Human cathelicidin, Claudin-1, Defensins, Hepcidin, Lactoferrin, Casein, Plectasin, Micrococcin P1, Scorpion venom, and Synthetic peptides were reviewed with antiviral properties against HBV and HCV.
Insights
Antimicrobial peptides (AMPs) show promise as a new treatment for Hepatitis C (HCV) and Hepatitis B (HBV) infections. These peptides offer a low-toxicity alternative to current therapies facing drug resistance and side effects.
Area of Science:
- Biochemistry
- Immunology
- Virology
Background:
- Hepatitis C (HCV) and Hepatitis B (HBV) infections present treatment challenges, including drug resistance, high costs, and adverse effects.
- Antimicrobial peptides (AMPs), naturally occurring immune molecules, are explored as alternative antiviral agents.
- AMPs possess amphiphilic properties and are found across prokaryotic and eukaryotic organisms.
Purpose of the Study:
- To review the potential of AMPs as an alternative therapeutic strategy for HCV and HBV infections.
- To highlight the mechanisms of action and low toxicity of AMPs against viral pathogens.
- To identify various AMPs with demonstrated antiviral properties against HBV and HCV.
Main Methods:
- Literature review of existing studies on AMPs and their antiviral activities.
- Analysis of AMPs' chemical characteristics, including amphiphilicity and charge.
- Examination of documented antiviral mechanisms of AMPs.
Main Results:
- AMPs exhibit diverse antiviral mechanisms, including inhibition of viral entry, replication, and packaging, alongside immune modulation.
- Several classes of AMPs, such as defensins and lactoferrin, demonstrate significant antiviral effects against HBV and HCV.
- AMPs show low toxicity to human host cells, particularly liver cells, making them suitable for therapeutic development.
Conclusions:
- AMPs represent a promising new generation of antiviral biomolecules for treating HCV and HBV infections.
- Their low toxicity and broad-spectrum activity position AMPs as valuable candidates for adjuvant therapy development.
- Further research into AMPs could lead to novel strategies to overcome current limitations in hepatitis treatment.
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