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TIRAP (MAL) S180L polymorphism is a common protective factor against developing tuberculosis and systemic lupus erythematosus
dc.creator | Castiblanco, John | spa |
dc.creator | Varela, Diana-Cristina | spa |
dc.creator | Castaño-Rodríguez, Natalia | spa |
dc.creator | Rojas-Villarraga, Adriana | spa |
dc.creator | Hincapié, María-Eugenia | spa |
dc.creator | Anaya, Juan-Manuel | spa |
dc.date.accessioned | 2020-05-26T00:11:31Z | |
dc.date.available | 2020-05-26T00:11:31Z | |
dc.date.created | 2008 | spa |
dc.description.abstract | Background and aim: The involvement of Toll-like receptor (TLR)-mediated pathways in infectious and autoimmunity has been suggested. The MyD88 adaptor-like (Mal) protein, also known as the TIR domain-containing adaptor protein (TIRAP), is implicated in the TLR2- and TLR4-mediated MyD88-dependent signaling pathway. The aim of this study was to investigate the influence of the functional TIRAP (MAL) S180L polymorphism on tuberculosis (TB) and four autoimmune diseases namely: rheumatoid arthritis (RA), primary Sjögren's syndrome (pSS), systemic lupus erythematosus (SLE) and type 1 diabetes mellitus (T1D). Methods: This was a case-control and family based association study in which 1325 individuals from a well-defined Colombian population were involved. TIRAP (MAL) S180L genotyping was done by using a polymerase chain reaction-restriction fragment length polymorphism technique and by direct sequencing. Results: Leu180 allele was found to be a protective factor against developing TB (odd ratio (OR): 0.53, 95% confidence interval (CI): 0.29-0.97) and SLE (OR: 0.29, 95% CI: 0.14-0.61) while no significant influence on RA, pSS and T1D was observed. Conclusion: These results support the influence of TIRAP (MAL) S180L polymorphism on TB and indicate that TB and SLE might share a common immunogenetic pathway in the innate immune response. © 2008 Elsevier B.V. All rights reserved. | eng |
dc.format.mimetype | application/pdf | |
dc.identifier.doi | https://doi.org/10.1016/j.meegid.2008.03.001 | |
dc.identifier.issn | 15671348 | |
dc.identifier.uri | https://repository.urosario.edu.co/handle/10336/24308 | |
dc.language.iso | eng | spa |
dc.relation.citationEndPage | 544 | |
dc.relation.citationIssue | No. 5 | |
dc.relation.citationStartPage | 541 | |
dc.relation.citationTitle | Infection, Genetics and Evolution | |
dc.relation.citationVolume | Vol. 8 | |
dc.relation.ispartof | Infection, Genetics and Evolution, ISSN:15671348, Vol.8, No.5 (2008); pp. 541-544 | spa |
dc.relation.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-46749097334&doi=10.1016%2fj.meegid.2008.03.001&partnerID=40&md5=b93dfe0b884d0fc662eb3b63f8c7ec7d | spa |
dc.rights.accesRights | info:eu-repo/semantics/openAccess | |
dc.rights.acceso | Abierto (Texto Completo) | spa |
dc.source.instname | instname:Universidad del Rosario | spa |
dc.source.reponame | reponame:Repositorio Institucional EdocUR | spa |
dc.subject.keyword | Adaptor protein | spa |
dc.subject.keyword | Leucine | spa |
dc.subject.keyword | systemic | eng |
dc.subject.keyword | interleukin-1 | eng |
dc.subject.keyword | genetic | eng |
dc.subject.keyword | Toll like receptor domain containing adaptor protein | spa |
dc.subject.keyword | Adult | spa |
dc.subject.keyword | Allele | spa |
dc.subject.keyword | Article | spa |
dc.subject.keyword | Autoimmune disease | spa |
dc.subject.keyword | Case control study | spa |
dc.subject.keyword | Colombia | spa |
dc.subject.keyword | Confidence interval | spa |
dc.subject.keyword | Controlled study | spa |
dc.subject.keyword | Family | spa |
dc.subject.keyword | Female | spa |
dc.subject.keyword | Gene sequence | spa |
dc.subject.keyword | Genetic polymorphism | spa |
dc.subject.keyword | Genetic susceptibility | spa |
dc.subject.keyword | Genotype | spa |
dc.subject.keyword | Human | spa |
dc.subject.keyword | Innate immunity | spa |
dc.subject.keyword | Insulin dependent diabetes mellitus | spa |
dc.subject.keyword | Major clinical study | spa |
dc.subject.keyword | Male | spa |
dc.subject.keyword | Polymerase chain reaction | spa |
dc.subject.keyword | Priority journal | spa |
dc.subject.keyword | Protection | spa |
dc.subject.keyword | Restriction fragment length polymorphism | spa |
dc.subject.keyword | Rheumatoid arthritis | spa |
dc.subject.keyword | Sjoegren syndrome | spa |
dc.subject.keyword | Systemic lupus erythematosus | spa |
dc.subject.keyword | Tuberculosis | spa |
dc.subject.keyword | Adult | spa |
dc.subject.keyword | Case-control studies | spa |
dc.subject.keyword | Colombia | spa |
dc.subject.keyword | Female | spa |
dc.subject.keyword | Gene frequency | spa |
dc.subject.keyword | Genotype | spa |
dc.subject.keyword | Humans | spa |
dc.subject.keyword | Lupus erythematosus | eng |
dc.subject.keyword | Male | spa |
dc.subject.keyword | Membrane glycoproteins | spa |
dc.subject.keyword | Middle aged | spa |
dc.subject.keyword | Polymorphism | eng |
dc.subject.keyword | Receptors | eng |
dc.subject.keyword | Tuberculosis | spa |
dc.subject.keyword | Mal | spa |
dc.subject.keyword | Rheumatoid arthritis | spa |
dc.subject.keyword | Sjögren's syndrome | spa |
dc.subject.keyword | Systemic lupus erythematosus | spa |
dc.subject.keyword | Tirap | spa |
dc.subject.keyword | Tuberculosis | spa |
dc.subject.keyword | Type 1 diabetes mellitus | spa |
dc.title | TIRAP (MAL) S180L polymorphism is a common protective factor against developing tuberculosis and systemic lupus erythematosus | spa |
dc.type | article | eng |
dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | |
dc.type.spa | Artículo | spa |
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