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IL-10 and TNFα Genotypes in SLE
The production of two regulators of the inflammatory response, interleukin 10 (IL-10) and tumor necrosis factor α (TNFα), has been found to be deeply deregulated in SLE patients, suggesting that these cytokines may be involved in the pathogenesis of the disease. Genetic polymorphisms at the promoter...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896901/ https://www.ncbi.nlm.nih.gov/pubmed/20625422 http://dx.doi.org/10.1155/2010/838390 |
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author | López, Patricia Gutiérrez, Carmen Suárez, Ana |
author_facet | López, Patricia Gutiérrez, Carmen Suárez, Ana |
author_sort | López, Patricia |
collection | PubMed |
description | The production of two regulators of the inflammatory response, interleukin 10 (IL-10) and tumor necrosis factor α (TNFα), has been found to be deeply deregulated in SLE patients, suggesting that these cytokines may be involved in the pathogenesis of the disease. Genetic polymorphisms at the promoter regions of IL-10 and TNFα genes have been associated with different constitutive and induced cytokine production. Given that individual steady-state levels of these molecules may deviate an initial immune response towards different forms of lymphocyte activation, functional genetic variants in their promoters could influence the development of SLE. The present review summarizes the information previously reported about the involvement of IL-10 and TNFα genetic variants on SLE appearance, clinical phenotype, and outcome. We show that, in spite of the heterogeneity of the populations studied, the existing knowledge points towards a relevant role of IL-10 and TNFα genotypes in SLE. |
format | Text |
id | pubmed-2896901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-28969012010-07-12 IL-10 and TNFα Genotypes in SLE López, Patricia Gutiérrez, Carmen Suárez, Ana J Biomed Biotechnol Review Article The production of two regulators of the inflammatory response, interleukin 10 (IL-10) and tumor necrosis factor α (TNFα), has been found to be deeply deregulated in SLE patients, suggesting that these cytokines may be involved in the pathogenesis of the disease. Genetic polymorphisms at the promoter regions of IL-10 and TNFα genes have been associated with different constitutive and induced cytokine production. Given that individual steady-state levels of these molecules may deviate an initial immune response towards different forms of lymphocyte activation, functional genetic variants in their promoters could influence the development of SLE. The present review summarizes the information previously reported about the involvement of IL-10 and TNFα genetic variants on SLE appearance, clinical phenotype, and outcome. We show that, in spite of the heterogeneity of the populations studied, the existing knowledge points towards a relevant role of IL-10 and TNFα genotypes in SLE. Hindawi Publishing Corporation 2010 2010-06-21 /pmc/articles/PMC2896901/ /pubmed/20625422 http://dx.doi.org/10.1155/2010/838390 Text en Copyright © 2010 Patricia López et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article López, Patricia Gutiérrez, Carmen Suárez, Ana IL-10 and TNFα Genotypes in SLE |
title | IL-10 and TNFα Genotypes in SLE |
title_full | IL-10 and TNFα Genotypes in SLE |
title_fullStr | IL-10 and TNFα Genotypes in SLE |
title_full_unstemmed | IL-10 and TNFα Genotypes in SLE |
title_short | IL-10 and TNFα Genotypes in SLE |
title_sort | il-10 and tnfα genotypes in sle |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896901/ https://www.ncbi.nlm.nih.gov/pubmed/20625422 http://dx.doi.org/10.1155/2010/838390 |
work_keys_str_mv | AT lopezpatricia il10andtnfagenotypesinsle AT gutierrezcarmen il10andtnfagenotypesinsle AT suarezana il10andtnfagenotypesinsle |