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CTLA4 Autoimmunity-Associated Genotype Contributes to Severe Pulmonary Tuberculosis in an African Population
The gene of Cytotoxic T Lymphocyte-associated Antigen 4 (CTLA4), a negative regulator of T lymphocytes, contains a single-nucleotide polymorphism (SNP) at position +6230A->G (ct60A->G), which has been found associated with several autoimmune diseases and appears to reduce T-cell inhibitory act...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2707621/ https://www.ncbi.nlm.nih.gov/pubmed/19609446 http://dx.doi.org/10.1371/journal.pone.0006307 |
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author | Thye, Thorsten Scarisbrick, Genevieve Browne, Edmund N. L. Chinbuah, Margaret Amanua Gyapong, John Osei, Ivy Owusu-Dabo, Ellis Niemann, Stefan Rüsch-Gerdes, Sabine Meyer, Christian G. Horstmann, Rolf D. |
author_facet | Thye, Thorsten Scarisbrick, Genevieve Browne, Edmund N. L. Chinbuah, Margaret Amanua Gyapong, John Osei, Ivy Owusu-Dabo, Ellis Niemann, Stefan Rüsch-Gerdes, Sabine Meyer, Christian G. Horstmann, Rolf D. |
author_sort | Thye, Thorsten |
collection | PubMed |
description | The gene of Cytotoxic T Lymphocyte-associated Antigen 4 (CTLA4), a negative regulator of T lymphocytes, contains a single-nucleotide polymorphism (SNP) at position +6230A->G (ct60A->G), which has been found associated with several autoimmune diseases and appears to reduce T-cell inhibitory activity. In Ghana, West Africa, we compared the frequencies of CTLA4 +6230 A/G and 6 haplotype-tagging SNPs in 2010 smear-positive, HIV-negative patients with pulmonary tuberculosis (TB) and 2346 controls matched for age, gender and ethnicity. We found no difference in allele frequencies between cases and controls. However, +6230A and a distinct CTLA4 haplotype and a diplotype comprising the +6230A allele were significantly less frequent among cases with large opacities in chest radiographs compared to those with small ones (P(corrected [cor]) = 0.002, P(cor) = 0.00045, P = 0.0005, respectively). This finding suggests that an increased T-cell activity associated with the CTLA4 +6230G allele contributes to pathology rather than to protection in pulmonary TB. |
format | Text |
id | pubmed-2707621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27076212009-07-17 CTLA4 Autoimmunity-Associated Genotype Contributes to Severe Pulmonary Tuberculosis in an African Population Thye, Thorsten Scarisbrick, Genevieve Browne, Edmund N. L. Chinbuah, Margaret Amanua Gyapong, John Osei, Ivy Owusu-Dabo, Ellis Niemann, Stefan Rüsch-Gerdes, Sabine Meyer, Christian G. Horstmann, Rolf D. PLoS One Research Article The gene of Cytotoxic T Lymphocyte-associated Antigen 4 (CTLA4), a negative regulator of T lymphocytes, contains a single-nucleotide polymorphism (SNP) at position +6230A->G (ct60A->G), which has been found associated with several autoimmune diseases and appears to reduce T-cell inhibitory activity. In Ghana, West Africa, we compared the frequencies of CTLA4 +6230 A/G and 6 haplotype-tagging SNPs in 2010 smear-positive, HIV-negative patients with pulmonary tuberculosis (TB) and 2346 controls matched for age, gender and ethnicity. We found no difference in allele frequencies between cases and controls. However, +6230A and a distinct CTLA4 haplotype and a diplotype comprising the +6230A allele were significantly less frequent among cases with large opacities in chest radiographs compared to those with small ones (P(corrected [cor]) = 0.002, P(cor) = 0.00045, P = 0.0005, respectively). This finding suggests that an increased T-cell activity associated with the CTLA4 +6230G allele contributes to pathology rather than to protection in pulmonary TB. Public Library of Science 2009-07-17 /pmc/articles/PMC2707621/ /pubmed/19609446 http://dx.doi.org/10.1371/journal.pone.0006307 Text en Thye et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Thye, Thorsten Scarisbrick, Genevieve Browne, Edmund N. L. Chinbuah, Margaret Amanua Gyapong, John Osei, Ivy Owusu-Dabo, Ellis Niemann, Stefan Rüsch-Gerdes, Sabine Meyer, Christian G. Horstmann, Rolf D. CTLA4 Autoimmunity-Associated Genotype Contributes to Severe Pulmonary Tuberculosis in an African Population |
title |
CTLA4 Autoimmunity-Associated Genotype Contributes to Severe Pulmonary Tuberculosis in an African Population |
title_full |
CTLA4 Autoimmunity-Associated Genotype Contributes to Severe Pulmonary Tuberculosis in an African Population |
title_fullStr |
CTLA4 Autoimmunity-Associated Genotype Contributes to Severe Pulmonary Tuberculosis in an African Population |
title_full_unstemmed |
CTLA4 Autoimmunity-Associated Genotype Contributes to Severe Pulmonary Tuberculosis in an African Population |
title_short |
CTLA4 Autoimmunity-Associated Genotype Contributes to Severe Pulmonary Tuberculosis in an African Population |
title_sort | ctla4 autoimmunity-associated genotype contributes to severe pulmonary tuberculosis in an african population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2707621/ https://www.ncbi.nlm.nih.gov/pubmed/19609446 http://dx.doi.org/10.1371/journal.pone.0006307 |
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