Genotypic analysis of Asp299Gly and Thr399Ile polymorphisms of TLR4 in Egyptian patients with rheumatoid arthritis and systemic lupus

Background Toll-like receptors (TLRs) are essential molecules of the innate immune system that stimulate numerous inflammatory pathways and harmonize systemic defense against a wide array of pathogens. TLRs may also recognize a number of self-proteins and endogenous nucleic acids. Inappropriate sti...

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Main Authors: Hanan A. Taha, Rania E. Sheir, Sanaa S Abdel Shafy, Lamya M. Mohamed
Format: Article
Language:English
Published: SpringerOpen 2014-01-01
Series:The Egyptian Journal of Internal Medicine
Subjects:
Online Access:http://www.esim.eg.net/article.asp?issn=1110-7782;year=2014;volume=26;issue=1;spage=15;epage=20;aulast=Taha
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author Hanan A. Taha
Rania E. Sheir
Sanaa S Abdel Shafy
Lamya M. Mohamed
author_facet Hanan A. Taha
Rania E. Sheir
Sanaa S Abdel Shafy
Lamya M. Mohamed
author_sort Hanan A. Taha
collection DOAJ
description Background Toll-like receptors (TLRs) are essential molecules of the innate immune system that stimulate numerous inflammatory pathways and harmonize systemic defense against a wide array of pathogens. TLRs may also recognize a number of self-proteins and endogenous nucleic acids. Inappropriate stimulation of the TLR pathway by endogenous or exogenous ligands or as a consequence of mutation in the TLR genes may lead to induction and/or prolongation of autoimmune response and tissue injury. This study was designed to detect the TLR4 (Asp299Gly and Thr399Ile) gene polymorphism in Egyptian patients with rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) as well as its correlation with disease activity. Participants and methods This study enrolled 50 patients who were attending the internal medicine and immunology out-patient clinic of Beni-Suef University Hospital. They were classified into three groups: 20 patients with RA, 20 patients with SLE, and 10 healthy controls. All studied persons were subjected to complete clinical evaluation, laboratory investigations, and detection of mutation in the TLR4 (Asp299Gly and Thr399Ile) gene by PCR technique. Results No individual in the RA patients group, the SLE patients group, or control population was identified carrying the Asp299Gly and Thr399Ile polymorphisms; in other words, all RA patients, SLE patients, and controls were with the same wild genotype. Conclusion The similarity in genotype between the patients group and control population concluded that these two missense polymorphisms do not contribute to RA and SLE in a group of Egyptian population.
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spelling doaj.art-cb54da9e09a54215aa949e25949c92b82022-12-22T00:59:36ZengSpringerOpenThe Egyptian Journal of Internal Medicine1110-77822090-90982014-01-01261152010.4103/1110-7782.132884Genotypic analysis of Asp299Gly and Thr399Ile polymorphisms of TLR4 in Egyptian patients with rheumatoid arthritis and systemic lupusHanan A. TahaRania E. SheirSanaa S Abdel ShafyLamya M. MohamedBackground Toll-like receptors (TLRs) are essential molecules of the innate immune system that stimulate numerous inflammatory pathways and harmonize systemic defense against a wide array of pathogens. TLRs may also recognize a number of self-proteins and endogenous nucleic acids. Inappropriate stimulation of the TLR pathway by endogenous or exogenous ligands or as a consequence of mutation in the TLR genes may lead to induction and/or prolongation of autoimmune response and tissue injury. This study was designed to detect the TLR4 (Asp299Gly and Thr399Ile) gene polymorphism in Egyptian patients with rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) as well as its correlation with disease activity. Participants and methods This study enrolled 50 patients who were attending the internal medicine and immunology out-patient clinic of Beni-Suef University Hospital. They were classified into three groups: 20 patients with RA, 20 patients with SLE, and 10 healthy controls. All studied persons were subjected to complete clinical evaluation, laboratory investigations, and detection of mutation in the TLR4 (Asp299Gly and Thr399Ile) gene by PCR technique. Results No individual in the RA patients group, the SLE patients group, or control population was identified carrying the Asp299Gly and Thr399Ile polymorphisms; in other words, all RA patients, SLE patients, and controls were with the same wild genotype. Conclusion The similarity in genotype between the patients group and control population concluded that these two missense polymorphisms do not contribute to RA and SLE in a group of Egyptian population.http://www.esim.eg.net/article.asp?issn=1110-7782;year=2014;volume=26;issue=1;spage=15;epage=20;aulast=TahaEgypt, polymorphism, rheumatoid arthritis, systemic lupus erythematosus, toll-like receptor
spellingShingle Hanan A. Taha
Rania E. Sheir
Sanaa S Abdel Shafy
Lamya M. Mohamed
Genotypic analysis of Asp299Gly and Thr399Ile polymorphisms of TLR4 in Egyptian patients with rheumatoid arthritis and systemic lupus
The Egyptian Journal of Internal Medicine
Egypt, polymorphism, rheumatoid arthritis, systemic lupus erythematosus, toll-like receptor
title Genotypic analysis of Asp299Gly and Thr399Ile polymorphisms of TLR4 in Egyptian patients with rheumatoid arthritis and systemic lupus
title_full Genotypic analysis of Asp299Gly and Thr399Ile polymorphisms of TLR4 in Egyptian patients with rheumatoid arthritis and systemic lupus
title_fullStr Genotypic analysis of Asp299Gly and Thr399Ile polymorphisms of TLR4 in Egyptian patients with rheumatoid arthritis and systemic lupus
title_full_unstemmed Genotypic analysis of Asp299Gly and Thr399Ile polymorphisms of TLR4 in Egyptian patients with rheumatoid arthritis and systemic lupus
title_short Genotypic analysis of Asp299Gly and Thr399Ile polymorphisms of TLR4 in Egyptian patients with rheumatoid arthritis and systemic lupus
title_sort genotypic analysis of asp299gly and thr399ile polymorphisms of tlr4 in egyptian patients with rheumatoid arthritis and systemic lupus
topic Egypt, polymorphism, rheumatoid arthritis, systemic lupus erythematosus, toll-like receptor
url http://www.esim.eg.net/article.asp?issn=1110-7782;year=2014;volume=26;issue=1;spage=15;epage=20;aulast=Taha
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