Interleukin-1? polymorphisms in Colombian patients with autoimmune rheumatic diseases

Interleukin-1 beta (IL-1?) exerts a range of inflammatory and immunomodulatory activities that are important in host defense and autoimmune response. The IL-1? gene, located on chromosome 2 (2q13), is polymorphic. The influence of its polymorphism on 355 patients with autoimmune rheumatic diseases w...

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Fecha de publicación:
2004
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/27895
Acceso en línea:
https://doi.org/10.1038/sj.gene.6364133
https://repository.urosario.edu.co/handle/10336/27895
Palabra clave:
Interleukin-1 beta
Polymorphisms
Sjögren's syndrome
Rheumatoid arthritis
Systemic lupus erythematosus
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spelling e038806a-b13c-46c8-a3df-a975e89a1de0c3fc4d67-260e-44b8-bb5c-1992e5387a492aa1f736-e919-4a89-bd9d-f56f9a9d1f1f194747786002020-08-19T14:44:30Z2020-08-19T14:44:30Z2004-10-07Interleukin-1 beta (IL-1?) exerts a range of inflammatory and immunomodulatory activities that are important in host defense and autoimmune response. The IL-1? gene, located on chromosome 2 (2q13), is polymorphic. The influence of its polymorphism on 355 patients with autoimmune rheumatic diseases was examined. To this effect, 172 patients with rheumatoid arthritis (RA), 114 with systemic lupus erythematosus (SLE), and 69 with primary Sjögren's syndrome (pSS) were studied. The control group consisted of 392 matched healthy individuals. Genotyping of IL-1? single-nucleotide polymorphisms (SNPs) at positions ?511 (C/T) and +3953 (C/T) was performed by the polymerase chain reaction-restriction fragment length polymorphism technique. In addition, levels of IL-1? were measured by immunoassay in supernatants of lipopolysaccharide (LPS)-stimulated and nonstimulated peripheral blood monocytes (PBM) obtained from 19 homozygous individuals for the three most common IL-1? likely haplotypes, all belonging to the control group. Allele+3953T was protective for SLE (odds ratio (OR)=0.57, 95% confidence intervals (CI)=0.34–0.88, P=0.01) as was the haplotype ?511C+3953T (OR=0.43, 95%CI=0.25–0.74, pc=0.006). The latter was associated with a lower LPS-stimulated-PBM IL-1? secretion. Results suggest that IL-1? polymorphism influences the susceptibility to acquire SLE in our population. The protective association might be explained by the observed inhibitory effect of IL-1? +3953T allele on the secretion of IL-1? under inflammatory circumstances.application/pdfhttps://doi.org/10.1038/sj.gene.6364133ISSN: 1466-4879EISSN: 1476-5470https://repository.urosario.edu.co/handle/10336/27895engNature Publishing Group614No. 8609Genes and ImmunityVol. 5Genes and Immunity, ISSN: 1466-4879;EISSN: 1476-5470, Vol.5, No.8 (2004); pp. 609–614https://www.nature.com/articles/6364133.pdfAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Genes and Immunityinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURInterleukin-1 betaPolymorphismsSjögren's syndromeRheumatoid arthritisSystemic lupus erythematosusInterleukin-1? polymorphisms in Colombian patients with autoimmune rheumatic diseasesPolimorfismos de interleucina-1? en pacientes colombianos con enfermedades reumáticas autoinmunesarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Camargo, J FCorrea, P ACastiblanco, JAnaya, Juan-ManuelORIGINAL6364133.pdfapplication/pdf158804https://repository.urosario.edu.co/bitstreams/15cd2130-cbed-482e-8e2a-b797e3e94f1e/downloadaf0e966ed2066804a1e2e8e63e5f673aMD51TEXT6364133.pdf.txt6364133.pdf.txtExtracted texttext/plain31984https://repository.urosario.edu.co/bitstreams/199a4673-54da-4cad-a9b4-b139ba00e1c9/download901d3f745675144fd83fdf6980c9e7a6MD52THUMBNAIL6364133.pdf.jpg6364133.pdf.jpgGenerated Thumbnailimage/jpeg5240https://repository.urosario.edu.co/bitstreams/0c1d0647-4c66-4b82-8580-ba20fefca1f4/download3bddf30877cf48d91f59a512082d3f2eMD5310336/27895oai:repository.urosario.edu.co:10336/278952021-08-10 23:03:55.959https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Interleukin-1? polymorphisms in Colombian patients with autoimmune rheumatic diseases
dc.title.TranslatedTitle.spa.fl_str_mv Polimorfismos de interleucina-1? en pacientes colombianos con enfermedades reumáticas autoinmunes
title Interleukin-1? polymorphisms in Colombian patients with autoimmune rheumatic diseases
spellingShingle Interleukin-1? polymorphisms in Colombian patients with autoimmune rheumatic diseases
Interleukin-1 beta
Polymorphisms
Sjögren's syndrome
Rheumatoid arthritis
Systemic lupus erythematosus
title_short Interleukin-1? polymorphisms in Colombian patients with autoimmune rheumatic diseases
title_full Interleukin-1? polymorphisms in Colombian patients with autoimmune rheumatic diseases
title_fullStr Interleukin-1? polymorphisms in Colombian patients with autoimmune rheumatic diseases
title_full_unstemmed Interleukin-1? polymorphisms in Colombian patients with autoimmune rheumatic diseases
title_sort Interleukin-1? polymorphisms in Colombian patients with autoimmune rheumatic diseases
dc.subject.keyword.spa.fl_str_mv Interleukin-1 beta
Polymorphisms
Sjögren's syndrome
Rheumatoid arthritis
Systemic lupus erythematosus
topic Interleukin-1 beta
Polymorphisms
Sjögren's syndrome
Rheumatoid arthritis
Systemic lupus erythematosus
description Interleukin-1 beta (IL-1?) exerts a range of inflammatory and immunomodulatory activities that are important in host defense and autoimmune response. The IL-1? gene, located on chromosome 2 (2q13), is polymorphic. The influence of its polymorphism on 355 patients with autoimmune rheumatic diseases was examined. To this effect, 172 patients with rheumatoid arthritis (RA), 114 with systemic lupus erythematosus (SLE), and 69 with primary Sjögren's syndrome (pSS) were studied. The control group consisted of 392 matched healthy individuals. Genotyping of IL-1? single-nucleotide polymorphisms (SNPs) at positions ?511 (C/T) and +3953 (C/T) was performed by the polymerase chain reaction-restriction fragment length polymorphism technique. In addition, levels of IL-1? were measured by immunoassay in supernatants of lipopolysaccharide (LPS)-stimulated and nonstimulated peripheral blood monocytes (PBM) obtained from 19 homozygous individuals for the three most common IL-1? likely haplotypes, all belonging to the control group. Allele+3953T was protective for SLE (odds ratio (OR)=0.57, 95% confidence intervals (CI)=0.34–0.88, P=0.01) as was the haplotype ?511C+3953T (OR=0.43, 95%CI=0.25–0.74, pc=0.006). The latter was associated with a lower LPS-stimulated-PBM IL-1? secretion. Results suggest that IL-1? polymorphism influences the susceptibility to acquire SLE in our population. The protective association might be explained by the observed inhibitory effect of IL-1? +3953T allele on the secretion of IL-1? under inflammatory circumstances.
publishDate 2004
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dc.date.accessioned.none.fl_str_mv 2020-08-19T14:44:30Z
dc.date.available.none.fl_str_mv 2020-08-19T14:44:30Z
dc.type.eng.fl_str_mv article
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dc.identifier.issn.none.fl_str_mv ISSN: 1466-4879
EISSN: 1476-5470
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https://repository.urosario.edu.co/handle/10336/27895
identifier_str_mv ISSN: 1466-4879
EISSN: 1476-5470
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dc.relation.citationIssue.none.fl_str_mv No. 8
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dc.relation.citationTitle.none.fl_str_mv Genes and Immunity
dc.relation.citationVolume.none.fl_str_mv Vol. 5
dc.relation.ispartof.spa.fl_str_mv Genes and Immunity, ISSN: 1466-4879;EISSN: 1476-5470, Vol.5, No.8 (2004); pp. 609–614
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