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Epigallocatechin gallate inhibits hepatitis B virus infection in human liver chimeric mice
BACKGROUND: Persistent hepatitis B virus (HBV) infection causes liver cirrhosis and hepatocellular carcinoma and constitutes a major worldwide health problem. Currently, anti-HBV drugs are limited to peginterferon and nucleos(t)ide analogs, which are costly and have considerable side effects; the de...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127945/ https://www.ncbi.nlm.nih.gov/pubmed/30189898 http://dx.doi.org/10.1186/s12906-018-2316-4 |
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author | Lai, Yu-Heng Sun, Cheng-Pu Huang, Hsiu-Chen Chen, Jui-Chieh Liu, Hui-Kang Huang, Cheng |
author_facet | Lai, Yu-Heng Sun, Cheng-Pu Huang, Hsiu-Chen Chen, Jui-Chieh Liu, Hui-Kang Huang, Cheng |
author_sort | Lai, Yu-Heng |
collection | PubMed |
description | BACKGROUND: Persistent hepatitis B virus (HBV) infection causes liver cirrhosis and hepatocellular carcinoma and constitutes a major worldwide health problem. Currently, anti-HBV drugs are limited to peginterferon and nucleos(t)ide analogs, which are costly and have considerable side effects; the development of novel, effective anti-HBV agents is crucial. METHODS: Catechins are a major group of compounds found in green tea extract and epigallocatechin gallate (EGCG) has been shown to have antiviral properties, including inhibition of cellular entry by HBV. FRG (Fah(−/−)/ Rag2(−/−)/ IL-2Rγ(/−)) mice were used in this study to generate chimeras carrying human primary hepatocytes, to facilitate investigation of the inhibitory effect of EGCG on HBV infection. RESULTS: Here, we show the inhibitory effect of EGCG on HBV infection and replication in HuS-E/2 cells. The inhibitory effect of EGCG on HBV infection in vivo was confirmed by monitoring HBV DNA and HBsAg in serum and immunostaining the liver tissues of the human liver chimeric mice. CONCLUSIONS: The effects of EGCG suggest a robust strategy for the treatment of HBV infection and EGCG may have therapeutic potential for the treatment of HBV-associated liver diseases. |
format | Online Article Text |
id | pubmed-6127945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61279452018-09-10 Epigallocatechin gallate inhibits hepatitis B virus infection in human liver chimeric mice Lai, Yu-Heng Sun, Cheng-Pu Huang, Hsiu-Chen Chen, Jui-Chieh Liu, Hui-Kang Huang, Cheng BMC Complement Altern Med Research Article BACKGROUND: Persistent hepatitis B virus (HBV) infection causes liver cirrhosis and hepatocellular carcinoma and constitutes a major worldwide health problem. Currently, anti-HBV drugs are limited to peginterferon and nucleos(t)ide analogs, which are costly and have considerable side effects; the development of novel, effective anti-HBV agents is crucial. METHODS: Catechins are a major group of compounds found in green tea extract and epigallocatechin gallate (EGCG) has been shown to have antiviral properties, including inhibition of cellular entry by HBV. FRG (Fah(−/−)/ Rag2(−/−)/ IL-2Rγ(/−)) mice were used in this study to generate chimeras carrying human primary hepatocytes, to facilitate investigation of the inhibitory effect of EGCG on HBV infection. RESULTS: Here, we show the inhibitory effect of EGCG on HBV infection and replication in HuS-E/2 cells. The inhibitory effect of EGCG on HBV infection in vivo was confirmed by monitoring HBV DNA and HBsAg in serum and immunostaining the liver tissues of the human liver chimeric mice. CONCLUSIONS: The effects of EGCG suggest a robust strategy for the treatment of HBV infection and EGCG may have therapeutic potential for the treatment of HBV-associated liver diseases. BioMed Central 2018-09-06 /pmc/articles/PMC6127945/ /pubmed/30189898 http://dx.doi.org/10.1186/s12906-018-2316-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Lai, Yu-Heng Sun, Cheng-Pu Huang, Hsiu-Chen Chen, Jui-Chieh Liu, Hui-Kang Huang, Cheng Epigallocatechin gallate inhibits hepatitis B virus infection in human liver chimeric mice |
title | Epigallocatechin gallate inhibits hepatitis B virus infection in human liver chimeric mice |
title_full | Epigallocatechin gallate inhibits hepatitis B virus infection in human liver chimeric mice |
title_fullStr | Epigallocatechin gallate inhibits hepatitis B virus infection in human liver chimeric mice |
title_full_unstemmed | Epigallocatechin gallate inhibits hepatitis B virus infection in human liver chimeric mice |
title_short | Epigallocatechin gallate inhibits hepatitis B virus infection in human liver chimeric mice |
title_sort | epigallocatechin gallate inhibits hepatitis b virus infection in human liver chimeric mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127945/ https://www.ncbi.nlm.nih.gov/pubmed/30189898 http://dx.doi.org/10.1186/s12906-018-2316-4 |
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