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Recent Advances in Hepatitis B Treatment

Hepatitis B virus infection affects over 250 million chronic carriers, causing more than 800,000 deaths annually, although a safe and effective vaccine is available. Currently used antiviral agents, pegylated interferon and nucleos(t)ide analogues, have major drawbacks and fail to completely eradica...

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Autores principales: Prifti, Georgia-Myrto, Moianos, Dimitrios, Giannakopoulou, Erofili, Pardali, Vasiliki, Tavis, John E., Zoidis, Grigoris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147224/
https://www.ncbi.nlm.nih.gov/pubmed/34062711
http://dx.doi.org/10.3390/ph14050417
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author Prifti, Georgia-Myrto
Moianos, Dimitrios
Giannakopoulou, Erofili
Pardali, Vasiliki
Tavis, John E.
Zoidis, Grigoris
author_facet Prifti, Georgia-Myrto
Moianos, Dimitrios
Giannakopoulou, Erofili
Pardali, Vasiliki
Tavis, John E.
Zoidis, Grigoris
author_sort Prifti, Georgia-Myrto
collection PubMed
description Hepatitis B virus infection affects over 250 million chronic carriers, causing more than 800,000 deaths annually, although a safe and effective vaccine is available. Currently used antiviral agents, pegylated interferon and nucleos(t)ide analogues, have major drawbacks and fail to completely eradicate the virus from infected cells. Thus, achieving a “functional cure” of the infection remains a real challenge. Recent findings concerning the viral replication cycle have led to development of novel therapeutic approaches including viral entry inhibitors, epigenetic control of cccDNA, immune modulators, RNA interference techniques, ribonuclease H inhibitors, and capsid assembly modulators. Promising preclinical results have been obtained, and the leading molecules under development have entered clinical evaluation. This review summarizes the key steps of the HBV life cycle, examines the currently approved anti-HBV drugs, and analyzes novel HBV treatment regimens.
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spelling pubmed-81472242021-05-26 Recent Advances in Hepatitis B Treatment Prifti, Georgia-Myrto Moianos, Dimitrios Giannakopoulou, Erofili Pardali, Vasiliki Tavis, John E. Zoidis, Grigoris Pharmaceuticals (Basel) Review Hepatitis B virus infection affects over 250 million chronic carriers, causing more than 800,000 deaths annually, although a safe and effective vaccine is available. Currently used antiviral agents, pegylated interferon and nucleos(t)ide analogues, have major drawbacks and fail to completely eradicate the virus from infected cells. Thus, achieving a “functional cure” of the infection remains a real challenge. Recent findings concerning the viral replication cycle have led to development of novel therapeutic approaches including viral entry inhibitors, epigenetic control of cccDNA, immune modulators, RNA interference techniques, ribonuclease H inhibitors, and capsid assembly modulators. Promising preclinical results have been obtained, and the leading molecules under development have entered clinical evaluation. This review summarizes the key steps of the HBV life cycle, examines the currently approved anti-HBV drugs, and analyzes novel HBV treatment regimens. MDPI 2021-05-01 /pmc/articles/PMC8147224/ /pubmed/34062711 http://dx.doi.org/10.3390/ph14050417 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Prifti, Georgia-Myrto
Moianos, Dimitrios
Giannakopoulou, Erofili
Pardali, Vasiliki
Tavis, John E.
Zoidis, Grigoris
Recent Advances in Hepatitis B Treatment
title Recent Advances in Hepatitis B Treatment
title_full Recent Advances in Hepatitis B Treatment
title_fullStr Recent Advances in Hepatitis B Treatment
title_full_unstemmed Recent Advances in Hepatitis B Treatment
title_short Recent Advances in Hepatitis B Treatment
title_sort recent advances in hepatitis b treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147224/
https://www.ncbi.nlm.nih.gov/pubmed/34062711
http://dx.doi.org/10.3390/ph14050417
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