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Association of IFNGR2 gene polymorphisms with pulmonary tuberculosis among the Vietnamese
Interferon-γ (IFN-γ) is a key molecule of T helper 1 (Th1)-immune response against tuberculosis (TB), and rare genetic defects of IFN-γ receptors cause disseminated mycobacterial infection. The aim of the present study was to investigate whether genetic polymorphisms found in the Th1-immune response...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325415/ https://www.ncbi.nlm.nih.gov/pubmed/22057826 http://dx.doi.org/10.1007/s00439-011-1112-8 |
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author | Hijikata, Minako Shojima, Junko Matsushita, Ikumi Tokunaga, Katsushi Ohashi, Jun Hang, Nguyen T. L. Horie, Toru Sakurada, Shinsaku Hoang, Nguyen P. Thuong, Pham H. Lien, Luu T. Keicho, Naoto |
author_facet | Hijikata, Minako Shojima, Junko Matsushita, Ikumi Tokunaga, Katsushi Ohashi, Jun Hang, Nguyen T. L. Horie, Toru Sakurada, Shinsaku Hoang, Nguyen P. Thuong, Pham H. Lien, Luu T. Keicho, Naoto |
author_sort | Hijikata, Minako |
collection | PubMed |
description | Interferon-γ (IFN-γ) is a key molecule of T helper 1 (Th1)-immune response against tuberculosis (TB), and rare genetic defects of IFN-γ receptors cause disseminated mycobacterial infection. The aim of the present study was to investigate whether genetic polymorphisms found in the Th1-immune response genes play a role in TB. In our study, DNA samples were collected from two series of cases including 832 patients with new smear-positive TB and 506 unrelated individuals with no history of TB in the general population of Hanoi, Vietnam. Alleles of eight microsatellite markers located around Th1-immune response-related genes and single nucleotide polymorphisms near the promising microsatellites were genotyped. A set of polymorphisms within the interferon gamma receptor 2 gene (IFNGR2) showed a significant association with protection against TB (P = 0.00054). Resistant alleles tend to be less frequently found in younger age at diagnosis (P = 0.011). Luciferase assays revealed high transcriptional activity of the promoter segment in linkage disequilibrium with resistant alleles. We conclude that the polymorphisms of IFNGR2 may confer resistance to the TB development of newly infected individuals. Contribution of the genetic factors to TB appeared to be different depending on age at diagnosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00439-011-1112-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3325415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-33254152012-04-20 Association of IFNGR2 gene polymorphisms with pulmonary tuberculosis among the Vietnamese Hijikata, Minako Shojima, Junko Matsushita, Ikumi Tokunaga, Katsushi Ohashi, Jun Hang, Nguyen T. L. Horie, Toru Sakurada, Shinsaku Hoang, Nguyen P. Thuong, Pham H. Lien, Luu T. Keicho, Naoto Hum Genet Original Investigation Interferon-γ (IFN-γ) is a key molecule of T helper 1 (Th1)-immune response against tuberculosis (TB), and rare genetic defects of IFN-γ receptors cause disseminated mycobacterial infection. The aim of the present study was to investigate whether genetic polymorphisms found in the Th1-immune response genes play a role in TB. In our study, DNA samples were collected from two series of cases including 832 patients with new smear-positive TB and 506 unrelated individuals with no history of TB in the general population of Hanoi, Vietnam. Alleles of eight microsatellite markers located around Th1-immune response-related genes and single nucleotide polymorphisms near the promising microsatellites were genotyped. A set of polymorphisms within the interferon gamma receptor 2 gene (IFNGR2) showed a significant association with protection against TB (P = 0.00054). Resistant alleles tend to be less frequently found in younger age at diagnosis (P = 0.011). Luciferase assays revealed high transcriptional activity of the promoter segment in linkage disequilibrium with resistant alleles. We conclude that the polymorphisms of IFNGR2 may confer resistance to the TB development of newly infected individuals. Contribution of the genetic factors to TB appeared to be different depending on age at diagnosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00439-011-1112-8) contains supplementary material, which is available to authorized users. Springer-Verlag 2011-11-06 2012 /pmc/articles/PMC3325415/ /pubmed/22057826 http://dx.doi.org/10.1007/s00439-011-1112-8 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Investigation Hijikata, Minako Shojima, Junko Matsushita, Ikumi Tokunaga, Katsushi Ohashi, Jun Hang, Nguyen T. L. Horie, Toru Sakurada, Shinsaku Hoang, Nguyen P. Thuong, Pham H. Lien, Luu T. Keicho, Naoto Association of IFNGR2 gene polymorphisms with pulmonary tuberculosis among the Vietnamese |
title | Association of IFNGR2 gene polymorphisms with pulmonary tuberculosis among the Vietnamese |
title_full | Association of IFNGR2 gene polymorphisms with pulmonary tuberculosis among the Vietnamese |
title_fullStr | Association of IFNGR2 gene polymorphisms with pulmonary tuberculosis among the Vietnamese |
title_full_unstemmed | Association of IFNGR2 gene polymorphisms with pulmonary tuberculosis among the Vietnamese |
title_short | Association of IFNGR2 gene polymorphisms with pulmonary tuberculosis among the Vietnamese |
title_sort | association of ifngr2 gene polymorphisms with pulmonary tuberculosis among the vietnamese |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325415/ https://www.ncbi.nlm.nih.gov/pubmed/22057826 http://dx.doi.org/10.1007/s00439-011-1112-8 |
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