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...

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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
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License
Restringido (Acceso a grupos específicos)
id EDOCUR2_f9999fd7d04ae0fe23dc15b2c55ad811
oai_identifier_str oai:repository.urosario.edu.co:10336/26049
network_acronym_str 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
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