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Development of Therapy Based on the Exploration of Biological Events Underlying the Pathogenetic Mechanisms of Chronic Hepatitis B Infection
According to the World Health Organization (WHO), an estimated 296 million people are chronically infected with hepatitis B virus (HBV). Approximately 15–25% of these people develop complications such as advanced chronic liver diseases (ACLDs). Mortality due to HBV-related complications accounted fo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376977/ https://www.ncbi.nlm.nih.gov/pubmed/37509583 http://dx.doi.org/10.3390/biomedicines11071944 |
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author | Akbar, Sheikh Mohammad Fazle Al Mahtab, Mamun Yoshida, Osamu Aguilar, Julio Gerardo, Guillen Nieto Hiasa, Yoichi |
author_facet | Akbar, Sheikh Mohammad Fazle Al Mahtab, Mamun Yoshida, Osamu Aguilar, Julio Gerardo, Guillen Nieto Hiasa, Yoichi |
author_sort | Akbar, Sheikh Mohammad Fazle |
collection | PubMed |
description | According to the World Health Organization (WHO), an estimated 296 million people are chronically infected with hepatitis B virus (HBV). Approximately 15–25% of these people develop complications such as advanced chronic liver diseases (ACLDs). Mortality due to HBV-related complications accounted for an estimated 882,000 deaths in 2019. Potent preventive vaccines have already restricted new HBV infections, and several drugs are available to treat chronic HBV infections. However, the positive impacts of these drugs have been recorded in only a few patients with chronic HBV infection. These drugs do not show long-term efficacy and cannot halt the progression to complications. Thus, more effective and evidence-based therapeutic strategies need to be urgently developed for patients with chronic HBV infection. CHB is a pathological entity induced by HBV that progresses due to impaired host immunity. This indicates the inherent limitations of antiviral-drug-based monotherapy for treating patients with chronic HBV infection. Additionally, commercially available antiviral drugs are not available to patients in developing and resource-constrained countries, posing a challenge to achieving the following WHO goal: “Elimination of Hepatitis by 2030”. As such, this review aimed to provide insights regarding evidence-based and effective management strategies for chronic HBV infection. |
format | Online Article Text |
id | pubmed-10376977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103769772023-07-29 Development of Therapy Based on the Exploration of Biological Events Underlying the Pathogenetic Mechanisms of Chronic Hepatitis B Infection Akbar, Sheikh Mohammad Fazle Al Mahtab, Mamun Yoshida, Osamu Aguilar, Julio Gerardo, Guillen Nieto Hiasa, Yoichi Biomedicines Review According to the World Health Organization (WHO), an estimated 296 million people are chronically infected with hepatitis B virus (HBV). Approximately 15–25% of these people develop complications such as advanced chronic liver diseases (ACLDs). Mortality due to HBV-related complications accounted for an estimated 882,000 deaths in 2019. Potent preventive vaccines have already restricted new HBV infections, and several drugs are available to treat chronic HBV infections. However, the positive impacts of these drugs have been recorded in only a few patients with chronic HBV infection. These drugs do not show long-term efficacy and cannot halt the progression to complications. Thus, more effective and evidence-based therapeutic strategies need to be urgently developed for patients with chronic HBV infection. CHB is a pathological entity induced by HBV that progresses due to impaired host immunity. This indicates the inherent limitations of antiviral-drug-based monotherapy for treating patients with chronic HBV infection. Additionally, commercially available antiviral drugs are not available to patients in developing and resource-constrained countries, posing a challenge to achieving the following WHO goal: “Elimination of Hepatitis by 2030”. As such, this review aimed to provide insights regarding evidence-based and effective management strategies for chronic HBV infection. MDPI 2023-07-08 /pmc/articles/PMC10376977/ /pubmed/37509583 http://dx.doi.org/10.3390/biomedicines11071944 Text en © 2023 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 Akbar, Sheikh Mohammad Fazle Al Mahtab, Mamun Yoshida, Osamu Aguilar, Julio Gerardo, Guillen Nieto Hiasa, Yoichi Development of Therapy Based on the Exploration of Biological Events Underlying the Pathogenetic Mechanisms of Chronic Hepatitis B Infection |
title | Development of Therapy Based on the Exploration of Biological Events Underlying the Pathogenetic Mechanisms of Chronic Hepatitis B Infection |
title_full | Development of Therapy Based on the Exploration of Biological Events Underlying the Pathogenetic Mechanisms of Chronic Hepatitis B Infection |
title_fullStr | Development of Therapy Based on the Exploration of Biological Events Underlying the Pathogenetic Mechanisms of Chronic Hepatitis B Infection |
title_full_unstemmed | Development of Therapy Based on the Exploration of Biological Events Underlying the Pathogenetic Mechanisms of Chronic Hepatitis B Infection |
title_short | Development of Therapy Based on the Exploration of Biological Events Underlying the Pathogenetic Mechanisms of Chronic Hepatitis B Infection |
title_sort | development of therapy based on the exploration of biological events underlying the pathogenetic mechanisms of chronic hepatitis b infection |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376977/ https://www.ncbi.nlm.nih.gov/pubmed/37509583 http://dx.doi.org/10.3390/biomedicines11071944 |
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