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HIV Infection and TLR Signalling in the Liver
Despite the availability of effective combination antiretroviral therapy (cART), liver disease is one of the leading causes of morbidity and mortality in Human Immunodeficiency Virus (HIV)-infected individuals, specifically, in the presence of viral hepatitis coinfection. HIV, a single stranded RNA...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296181/ https://www.ncbi.nlm.nih.gov/pubmed/22474436 http://dx.doi.org/10.1155/2012/473925 |
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author | Crane, Megan Visvanathan, Kumar Lewin, Sharon R. |
author_facet | Crane, Megan Visvanathan, Kumar Lewin, Sharon R. |
author_sort | Crane, Megan |
collection | PubMed |
description | Despite the availability of effective combination antiretroviral therapy (cART), liver disease is one of the leading causes of morbidity and mortality in Human Immunodeficiency Virus (HIV)-infected individuals, specifically, in the presence of viral hepatitis coinfection. HIV, a single stranded RNA virus, can bind to and activate both Toll-like receptor (TLR)7 and TLR8 in circulating blood mononuclear cells, but little is known about the effect of HIV on TLRs expressed in the liver. HIV can directly infect cells of the liver and HIV-mediated depletion of CD4+ T-cells in the gastrointestinal tract (GI tract) results in increased circulating lipopolysaccharide (LPS), both of which may impact on TLR signaling in the liver and subsequent liver disease progression. The potential direct and indirect effects of HIV on TLR signaling in the liver will be explored in this paper. |
format | Online Article Text |
id | pubmed-3296181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32961812012-04-03 HIV Infection and TLR Signalling in the Liver Crane, Megan Visvanathan, Kumar Lewin, Sharon R. Gastroenterol Res Pract Review Article Despite the availability of effective combination antiretroviral therapy (cART), liver disease is one of the leading causes of morbidity and mortality in Human Immunodeficiency Virus (HIV)-infected individuals, specifically, in the presence of viral hepatitis coinfection. HIV, a single stranded RNA virus, can bind to and activate both Toll-like receptor (TLR)7 and TLR8 in circulating blood mononuclear cells, but little is known about the effect of HIV on TLRs expressed in the liver. HIV can directly infect cells of the liver and HIV-mediated depletion of CD4+ T-cells in the gastrointestinal tract (GI tract) results in increased circulating lipopolysaccharide (LPS), both of which may impact on TLR signaling in the liver and subsequent liver disease progression. The potential direct and indirect effects of HIV on TLR signaling in the liver will be explored in this paper. Hindawi Publishing Corporation 2012 2012-02-22 /pmc/articles/PMC3296181/ /pubmed/22474436 http://dx.doi.org/10.1155/2012/473925 Text en Copyright © 2012 Megan Crane et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Crane, Megan Visvanathan, Kumar Lewin, Sharon R. HIV Infection and TLR Signalling in the Liver |
title | HIV Infection and TLR Signalling in the Liver |
title_full | HIV Infection and TLR Signalling in the Liver |
title_fullStr | HIV Infection and TLR Signalling in the Liver |
title_full_unstemmed | HIV Infection and TLR Signalling in the Liver |
title_short | HIV Infection and TLR Signalling in the Liver |
title_sort | hiv infection and tlr signalling in the liver |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296181/ https://www.ncbi.nlm.nih.gov/pubmed/22474436 http://dx.doi.org/10.1155/2012/473925 |
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