Autoimmunity and tuberculosis. Opposite association with TNF polymorphism
Objective. To examine the influence of the –308 and –238 single nucleotide polymorphisms (SNP) of tumor necrosis factor-? gene (TNF) on patients with systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), primary Sjögren’s syndrome (SS), and tuberculosis (TB). Methods. Genomic DNA from patie...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2005
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/26049
- Acceso en línea:
- https://repository.urosario.edu.co/handle/10336/26049
- Palabra clave:
- Tumor necrosis factor
Rheumatoid arthritis
Tuberculosis systemic lupus erythematosus
Sjögren’s Syndrome
Autoimmunity
- Rights
- License
- Restringido (Acceso a grupos específicos)
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EDOCUR2_f9999fd7d04ae0fe23dc15b2c55ad811 |
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oai:repository.urosario.edu.co:10336/26049 |
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EDOCUR2 |
network_name_str |
Repositorio EdocUR - U. Rosario |
repository_id_str |
|
spelling |
db6634cb-78db-456d-82d5-fa7140510037c0663320-d7f6-4932-b972-de85e975a964585274c5-42d7-4c99-8347-aa1cce3602b3194747786002020-08-06T16:20:32Z2020-08-06T16:20:32Z2005Objective. To examine the influence of the –308 and –238 single nucleotide polymorphisms (SNP) of tumor necrosis factor-? gene (TNF) on patients with systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), primary Sjögren’s syndrome (SS), and tuberculosis (TB). Methods. Genomic DNA from patients with RA (n = 165), SLE (n = 100), primary SS (n = 67), and TB (n = 135) and ethnically matched controls (n = 430) was genotyped for TNF –308 and –238 SNP by PCR-RFLP. Results. TNF –308A allele was associated with RA (odds ratio, OR 1.8, p = 0.002), SLE (OR 2.6, p < 0.0001), and primary SS (OR 2.9, p < 0.0001). TNF –308G was associated with TB (OR 1.8, p = 0.02). The –308 GG genotype was protective for autoimmunity (p < 0.003). TNF –238A allele was protective for autoimmunity but represented a susceptibility factor for TB (OR 2.2, p < 0.0001). Haplotype –308A–238G was a protective factor against TB, whereas it carried susceptibility for RA, SLE, and primary SS (p < 0.0001). Conclusion. The results show an opposite association of TNF polymorphism with autoimmunity and TB, and suggest the existence of heterozygote advantage, sustaining the hypothesis that autoimmune diseases are a consequence of natural selection for enhanced TB resistance. Data also provide genetic evidence supporting the common variants/multiple disease hypothesis, which emphasizes that many disease genes may not be disease-specific, and that similar immunogenetic mechanisms underlie autoimmune diseases. (J Rheumatol 2005;32:219–24)application/pdfISSN: 0315-162XEISSN: 1499-2752https://repository.urosario.edu.co/handle/10336/26049engCanadian Rheumatology Association224No. 2219Journal of RheumatologyVol. 32The Journal of Rheumatology, ISSN: 0315-162X;EISSN: 1499-2752, Vol.32, No.2 (february, 2005) pp.219-224https://www.jrheum.org/content/jrheum/32/2/219.full.pdfRestringido (Acceso a grupos específicos)http://purl.org/coar/access_right/c_16ecJournal of Rheumatologyinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURTumor necrosis factorRheumatoid arthritisTuberculosis systemic lupus erythematosusSjögren’s SyndromeAutoimmunityAutoimmunity and tuberculosis. Opposite association with TNF polymorphismAutoinmunidad y tuberculosis. Asociación opuesta con polimorfismo TNFarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Correa, Paula A.Gómez, Luis M.Cadena, JoseAnaya, Juan-Manuel10336/26049oai:repository.urosario.edu.co:10336/260492022-05-02 07:37:13.138655https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
Autoimmunity and tuberculosis. Opposite association with TNF polymorphism |
dc.title.TranslatedTitle.spa.fl_str_mv |
Autoinmunidad y tuberculosis. Asociación opuesta con polimorfismo TNF |
title |
Autoimmunity and tuberculosis. Opposite association with TNF polymorphism |
spellingShingle |
Autoimmunity and tuberculosis. Opposite association with TNF polymorphism Tumor necrosis factor Rheumatoid arthritis Tuberculosis systemic lupus erythematosus Sjögren’s Syndrome Autoimmunity |
title_short |
Autoimmunity and tuberculosis. Opposite association with TNF polymorphism |
title_full |
Autoimmunity and tuberculosis. Opposite association with TNF polymorphism |
title_fullStr |
Autoimmunity and tuberculosis. Opposite association with TNF polymorphism |
title_full_unstemmed |
Autoimmunity and tuberculosis. Opposite association with TNF polymorphism |
title_sort |
Autoimmunity and tuberculosis. Opposite association with TNF polymorphism |
dc.subject.keyword.spa.fl_str_mv |
Tumor necrosis factor Rheumatoid arthritis Tuberculosis systemic lupus erythematosus Sjögren’s Syndrome Autoimmunity |
topic |
Tumor necrosis factor Rheumatoid arthritis Tuberculosis systemic lupus erythematosus Sjögren’s Syndrome Autoimmunity |
description |
Objective. To examine the influence of the –308 and –238 single nucleotide polymorphisms (SNP) of tumor necrosis factor-? gene (TNF) on patients with systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), primary Sjögren’s syndrome (SS), and tuberculosis (TB). Methods. Genomic DNA from patients with RA (n = 165), SLE (n = 100), primary SS (n = 67), and TB (n = 135) and ethnically matched controls (n = 430) was genotyped for TNF –308 and –238 SNP by PCR-RFLP. Results. TNF –308A allele was associated with RA (odds ratio, OR 1.8, p = 0.002), SLE (OR 2.6, p < 0.0001), and primary SS (OR 2.9, p < 0.0001). TNF –308G was associated with TB (OR 1.8, p = 0.02). The –308 GG genotype was protective for autoimmunity (p < 0.003). TNF –238A allele was protective for autoimmunity but represented a susceptibility factor for TB (OR 2.2, p < 0.0001). Haplotype –308A–238G was a protective factor against TB, whereas it carried susceptibility for RA, SLE, and primary SS (p < 0.0001). Conclusion. The results show an opposite association of TNF polymorphism with autoimmunity and TB, and suggest the existence of heterozygote advantage, sustaining the hypothesis that autoimmune diseases are a consequence of natural selection for enhanced TB resistance. Data also provide genetic evidence supporting the common variants/multiple disease hypothesis, which emphasizes that many disease genes may not be disease-specific, and that similar immunogenetic mechanisms underlie autoimmune diseases. (J Rheumatol 2005;32:219–24) |
publishDate |
2005 |
dc.date.created.spa.fl_str_mv |
2005 |
dc.date.accessioned.none.fl_str_mv |
2020-08-06T16:20:32Z |
dc.date.available.none.fl_str_mv |
2020-08-06T16:20:32Z |
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.issn.none.fl_str_mv |
ISSN: 0315-162X EISSN: 1499-2752 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/26049 |
identifier_str_mv |
ISSN: 0315-162X EISSN: 1499-2752 |
url |
https://repository.urosario.edu.co/handle/10336/26049 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
224 |
dc.relation.citationIssue.none.fl_str_mv |
No. 2 |
dc.relation.citationStartPage.none.fl_str_mv |
219 |
dc.relation.citationTitle.none.fl_str_mv |
Journal of Rheumatology |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 32 |
dc.relation.ispartof.spa.fl_str_mv |
The Journal of Rheumatology, ISSN: 0315-162X;EISSN: 1499-2752, Vol.32, No.2 (february, 2005) pp.219-224 |
dc.relation.uri.spa.fl_str_mv |
https://www.jrheum.org/content/jrheum/32/2/219.full.pdf |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_16ec |
dc.rights.acceso.spa.fl_str_mv |
Restringido (Acceso a grupos específicos) |
rights_invalid_str_mv |
Restringido (Acceso a grupos específicos) http://purl.org/coar/access_right/c_16ec |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Canadian Rheumatology Association |
dc.source.spa.fl_str_mv |
Journal of Rheumatology |
institution |
Universidad del Rosario |
dc.source.instname.none.fl_str_mv |
instname:Universidad del Rosario |
dc.source.reponame.none.fl_str_mv |
reponame:Repositorio Institucional EdocUR |
repository.name.fl_str_mv |
Repositorio institucional EdocUR |
repository.mail.fl_str_mv |
edocur@urosario.edu.co |
_version_ |
1831928206574223360 |