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Evidence for Viral Induction of Biliary Atresia: A Review
Biliary atresia (BA) is a childhood disease which manifests with abnormal narrowing, blockage or complete absence of bile ducts within the liver. Many possible etiologies have been reported for the development of BA, including congenital, perinatal and acquired conditions. Since the 1970’s, there ha...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
XIA & HE Publishing Inc.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328731/ https://www.ncbi.nlm.nih.gov/pubmed/30637219 http://dx.doi.org/10.14218/JCTH.2018.00046 |
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author | Averbukh, Leon D. Wu, George Y. |
author_facet | Averbukh, Leon D. Wu, George Y. |
author_sort | Averbukh, Leon D. |
collection | PubMed |
description | Biliary atresia (BA) is a childhood disease which manifests with abnormal narrowing, blockage or complete absence of bile ducts within the liver. Many possible etiologies have been reported for the development of BA, including congenital, perinatal and acquired conditions. Since the 1970’s, there has been increasing evidence linking BA development to viral perinatal infections. The viral vectors most commonly implicated include members of the herpesviridae family (cytomegalovirus and Epstein-Barr virus) as well as those of the reoviridae family (reovirus and rotavirus). While extensive work has been done on a murine model of disease, the current review focuses primarily on evidence from human studies of viral vectors in children afflicted with BA. |
format | Online Article Text |
id | pubmed-6328731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | XIA & HE Publishing Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63287312019-01-11 Evidence for Viral Induction of Biliary Atresia: A Review Averbukh, Leon D. Wu, George Y. J Clin Transl Hepatol Review Article Biliary atresia (BA) is a childhood disease which manifests with abnormal narrowing, blockage or complete absence of bile ducts within the liver. Many possible etiologies have been reported for the development of BA, including congenital, perinatal and acquired conditions. Since the 1970’s, there has been increasing evidence linking BA development to viral perinatal infections. The viral vectors most commonly implicated include members of the herpesviridae family (cytomegalovirus and Epstein-Barr virus) as well as those of the reoviridae family (reovirus and rotavirus). While extensive work has been done on a murine model of disease, the current review focuses primarily on evidence from human studies of viral vectors in children afflicted with BA. XIA & HE Publishing Inc. 2018-11-14 2018-12-28 /pmc/articles/PMC6328731/ /pubmed/30637219 http://dx.doi.org/10.14218/JCTH.2018.00046 Text en © 2018 Authors. http://creativecommons.org/licenses/by-nc/4.0/ This article has been published under the terms of Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0), which permits noncommercial unrestricted use, distribution, and reproduction in any medium, provided that the following statement is provided. “This article has been published in Journal of Clinical and Translational Hepatology at DOI: 10.14218/JCTH.2018.00046 and can also be viewed on the Journal’s website at http://www.jcthnet.com”. |
spellingShingle | Review Article Averbukh, Leon D. Wu, George Y. Evidence for Viral Induction of Biliary Atresia: A Review |
title | Evidence for Viral Induction of Biliary Atresia: A Review |
title_full | Evidence for Viral Induction of Biliary Atresia: A Review |
title_fullStr | Evidence for Viral Induction of Biliary Atresia: A Review |
title_full_unstemmed | Evidence for Viral Induction of Biliary Atresia: A Review |
title_short | Evidence for Viral Induction of Biliary Atresia: A Review |
title_sort | evidence for viral induction of biliary atresia: a review |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328731/ https://www.ncbi.nlm.nih.gov/pubmed/30637219 http://dx.doi.org/10.14218/JCTH.2018.00046 |
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