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Advances in Immunotherapy for Hepatitis B
Hepatitis B virus (HBV) is a hepatotropic virus with the potential to cause chronic infection, and it is one of the common causes of liver disease worldwide. Chronic HBV infection leads to liver cirrhosis and, ultimately, hepatocellular carcinoma (HCC). The persistence of covalently closed circular...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612046/ https://www.ncbi.nlm.nih.gov/pubmed/36297173 http://dx.doi.org/10.3390/pathogens11101116 |
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author | Wang, Dongyao Fu, Binqing Wei, Haiming |
author_facet | Wang, Dongyao Fu, Binqing Wei, Haiming |
author_sort | Wang, Dongyao |
collection | PubMed |
description | Hepatitis B virus (HBV) is a hepatotropic virus with the potential to cause chronic infection, and it is one of the common causes of liver disease worldwide. Chronic HBV infection leads to liver cirrhosis and, ultimately, hepatocellular carcinoma (HCC). The persistence of covalently closed circular DNA (cccDNA) and the impaired immune response in patients with chronic hepatitis B (CHB) has been studied over the past few decades. Despite advances in the etiology of HBV and the development of potent virus-suppressing regimens, a cure for HBV has not been found. Both the innate and adaptive branches of immunity contribute to viral eradication. However, immune exhaustion and evasion have been demonstrated during CHB infection, although our understanding of the mechanism is still evolving. Recently, the successful use of an antiviral drug for hepatitis C has greatly encouraged the search for a cure for hepatitis B, which likely requires an approach focused on improving the antiviral immune response. In this review, we discuss our current knowledge of the immunopathogenic mechanisms and immunobiology of HBV infection. In addition, we touch upon why the existing therapeutic approaches may not achieve the goal of a functional cure. We also propose how combinations of new drugs, and especially novel immunotherapies, contribute to HBV clearance. |
format | Online Article Text |
id | pubmed-9612046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96120462022-10-28 Advances in Immunotherapy for Hepatitis B Wang, Dongyao Fu, Binqing Wei, Haiming Pathogens Review Hepatitis B virus (HBV) is a hepatotropic virus with the potential to cause chronic infection, and it is one of the common causes of liver disease worldwide. Chronic HBV infection leads to liver cirrhosis and, ultimately, hepatocellular carcinoma (HCC). The persistence of covalently closed circular DNA (cccDNA) and the impaired immune response in patients with chronic hepatitis B (CHB) has been studied over the past few decades. Despite advances in the etiology of HBV and the development of potent virus-suppressing regimens, a cure for HBV has not been found. Both the innate and adaptive branches of immunity contribute to viral eradication. However, immune exhaustion and evasion have been demonstrated during CHB infection, although our understanding of the mechanism is still evolving. Recently, the successful use of an antiviral drug for hepatitis C has greatly encouraged the search for a cure for hepatitis B, which likely requires an approach focused on improving the antiviral immune response. In this review, we discuss our current knowledge of the immunopathogenic mechanisms and immunobiology of HBV infection. In addition, we touch upon why the existing therapeutic approaches may not achieve the goal of a functional cure. We also propose how combinations of new drugs, and especially novel immunotherapies, contribute to HBV clearance. MDPI 2022-09-28 /pmc/articles/PMC9612046/ /pubmed/36297173 http://dx.doi.org/10.3390/pathogens11101116 Text en © 2022 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 Wang, Dongyao Fu, Binqing Wei, Haiming Advances in Immunotherapy for Hepatitis B |
title | Advances in Immunotherapy for Hepatitis B |
title_full | Advances in Immunotherapy for Hepatitis B |
title_fullStr | Advances in Immunotherapy for Hepatitis B |
title_full_unstemmed | Advances in Immunotherapy for Hepatitis B |
title_short | Advances in Immunotherapy for Hepatitis B |
title_sort | advances in immunotherapy for hepatitis b |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612046/ https://www.ncbi.nlm.nih.gov/pubmed/36297173 http://dx.doi.org/10.3390/pathogens11101116 |
work_keys_str_mv | AT wangdongyao advancesinimmunotherapyforhepatitisb AT fubinqing advancesinimmunotherapyforhepatitisb AT weihaiming advancesinimmunotherapyforhepatitisb |