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...
- Autores:
- Tipo de recurso:
- 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
- Rights
- License
- Abierto (Texto Completo)
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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 |
dc.date.created.spa.fl_str_mv |
2004-10-07 |
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 |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1038/sj.gene.6364133 |
dc.identifier.issn.none.fl_str_mv |
ISSN: 1466-4879 EISSN: 1476-5470 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/27895 |
url |
https://doi.org/10.1038/sj.gene.6364133 https://repository.urosario.edu.co/handle/10336/27895 |
identifier_str_mv |
ISSN: 1466-4879 EISSN: 1476-5470 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
614 |
dc.relation.citationIssue.none.fl_str_mv |
No. 8 |
dc.relation.citationStartPage.none.fl_str_mv |
609 |
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 |
dc.relation.uri.spa.fl_str_mv |
https://www.nature.com/articles/6364133.pdf |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
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Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
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Nature Publishing Group |
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Genes and Immunity |
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Universidad del Rosario |
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