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Association of Toll-Like Receptor 3 Single-Nucleotide Polymorphisms and Hepatitis C Virus Infection

Toll-like receptor 3 (TLR3) plays a key role in innate immunity by recognizing pathogenic, double-stranded RNAs. Thus, activation of TLR3 is a major factor in antiviral defense and tumor eradication. Although downregulation of TLR3 gene expression has been mainly reported in patients infected with h...

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Autores principales: Al-Anazi, Mashael R., Matou-Nasri, Sabine, Abdo, Ayman A., Sanai, Faisal M., Alkahtani, Saad, Alarifi, Saud, Alkahtane, Abdullah A., Al-Yahya, Hamad, Ali, Daoud, Alessia, Mohammed S., Alshahrani, Bushra, Al-Ahdal, Mohammed N., Al-Qahtani, Ahmed A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5239973/
https://www.ncbi.nlm.nih.gov/pubmed/28127569
http://dx.doi.org/10.1155/2017/1590653
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author Al-Anazi, Mashael R.
Matou-Nasri, Sabine
Abdo, Ayman A.
Sanai, Faisal M.
Alkahtani, Saad
Alarifi, Saud
Alkahtane, Abdullah A.
Al-Yahya, Hamad
Ali, Daoud
Alessia, Mohammed S.
Alshahrani, Bushra
Al-Ahdal, Mohammed N.
Al-Qahtani, Ahmed A.
author_facet Al-Anazi, Mashael R.
Matou-Nasri, Sabine
Abdo, Ayman A.
Sanai, Faisal M.
Alkahtani, Saad
Alarifi, Saud
Alkahtane, Abdullah A.
Al-Yahya, Hamad
Ali, Daoud
Alessia, Mohammed S.
Alshahrani, Bushra
Al-Ahdal, Mohammed N.
Al-Qahtani, Ahmed A.
author_sort Al-Anazi, Mashael R.
collection PubMed
description Toll-like receptor 3 (TLR3) plays a key role in innate immunity by recognizing pathogenic, double-stranded RNAs. Thus, activation of TLR3 is a major factor in antiviral defense and tumor eradication. Although downregulation of TLR3 gene expression has been mainly reported in patients infected with hepatitis C virus (HCV), the influence of TLR3 genotype on the risk of HCV infection, HCV-related cirrhosis, and/or hepatocellular carcinoma (HCC) remains to be determined. Single-nucleotide polymorphisms (SNPs) within the TLR3 gene and their associations with HCV-related disease risk were investigated in a Saudi Arabian population in this study. Eight TLR3 SNPs were analyzed in 563 patients with HCV, which consisted of 437 patients with chronic HCV infections, 88 with HCV-induced liver cirrhosis, and 38 with HCC. A total of 599 healthy control subjects were recruited to the study. Among the eight TLR3 SNPs studied, the rs78726532 SNP was strongly associated with HCV infection when compared to that in healthy control subjects. The rs5743314 was also strongly associated with HCV-related liver disease progression (cirrhosis and HCC). In summary, these results indicate that distinct genetic variants of TLR3 SNPs are associated with HCV infection and HCV-mediated liver disease progression in the Saudi Arabian population.
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spelling pubmed-52399732017-01-26 Association of Toll-Like Receptor 3 Single-Nucleotide Polymorphisms and Hepatitis C Virus Infection Al-Anazi, Mashael R. Matou-Nasri, Sabine Abdo, Ayman A. Sanai, Faisal M. Alkahtani, Saad Alarifi, Saud Alkahtane, Abdullah A. Al-Yahya, Hamad Ali, Daoud Alessia, Mohammed S. Alshahrani, Bushra Al-Ahdal, Mohammed N. Al-Qahtani, Ahmed A. J Immunol Res Research Article Toll-like receptor 3 (TLR3) plays a key role in innate immunity by recognizing pathogenic, double-stranded RNAs. Thus, activation of TLR3 is a major factor in antiviral defense and tumor eradication. Although downregulation of TLR3 gene expression has been mainly reported in patients infected with hepatitis C virus (HCV), the influence of TLR3 genotype on the risk of HCV infection, HCV-related cirrhosis, and/or hepatocellular carcinoma (HCC) remains to be determined. Single-nucleotide polymorphisms (SNPs) within the TLR3 gene and their associations with HCV-related disease risk were investigated in a Saudi Arabian population in this study. Eight TLR3 SNPs were analyzed in 563 patients with HCV, which consisted of 437 patients with chronic HCV infections, 88 with HCV-induced liver cirrhosis, and 38 with HCC. A total of 599 healthy control subjects were recruited to the study. Among the eight TLR3 SNPs studied, the rs78726532 SNP was strongly associated with HCV infection when compared to that in healthy control subjects. The rs5743314 was also strongly associated with HCV-related liver disease progression (cirrhosis and HCC). In summary, these results indicate that distinct genetic variants of TLR3 SNPs are associated with HCV infection and HCV-mediated liver disease progression in the Saudi Arabian population. Hindawi Publishing Corporation 2017 2017-01-03 /pmc/articles/PMC5239973/ /pubmed/28127569 http://dx.doi.org/10.1155/2017/1590653 Text en Copyright © 2017 Mashael R. Al-Anazi et al. https://creativecommons.org/licenses/by/4.0/ 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 Research Article
Al-Anazi, Mashael R.
Matou-Nasri, Sabine
Abdo, Ayman A.
Sanai, Faisal M.
Alkahtani, Saad
Alarifi, Saud
Alkahtane, Abdullah A.
Al-Yahya, Hamad
Ali, Daoud
Alessia, Mohammed S.
Alshahrani, Bushra
Al-Ahdal, Mohammed N.
Al-Qahtani, Ahmed A.
Association of Toll-Like Receptor 3 Single-Nucleotide Polymorphisms and Hepatitis C Virus Infection
title Association of Toll-Like Receptor 3 Single-Nucleotide Polymorphisms and Hepatitis C Virus Infection
title_full Association of Toll-Like Receptor 3 Single-Nucleotide Polymorphisms and Hepatitis C Virus Infection
title_fullStr Association of Toll-Like Receptor 3 Single-Nucleotide Polymorphisms and Hepatitis C Virus Infection
title_full_unstemmed Association of Toll-Like Receptor 3 Single-Nucleotide Polymorphisms and Hepatitis C Virus Infection
title_short Association of Toll-Like Receptor 3 Single-Nucleotide Polymorphisms and Hepatitis C Virus Infection
title_sort association of toll-like receptor 3 single-nucleotide polymorphisms and hepatitis c virus infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5239973/
https://www.ncbi.nlm.nih.gov/pubmed/28127569
http://dx.doi.org/10.1155/2017/1590653
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