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Analysis of HLA association among North Indian HIV-positive individuals co-infected with Mycobacterium tuberculosis
BACKGROUND: Genetic variation in HLA genes influence the immune response and may thus contribute to differential development of tuberculosis (TB) in HIV-infected individuals. The study was designed to determine whether HLA polymorphisms influence the development of Mycobacterium tuberculosis infecti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586997/ https://www.ncbi.nlm.nih.gov/pubmed/26628757 http://dx.doi.org/10.4103/0970-2113.164166 |
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author | Saikia, Biman Wanchu, Ajay Mahakur, Sobhana Bind, Mahendra Sarkar, Krishnakali Minz, Ranjana W |
author_facet | Saikia, Biman Wanchu, Ajay Mahakur, Sobhana Bind, Mahendra Sarkar, Krishnakali Minz, Ranjana W |
author_sort | Saikia, Biman |
collection | PubMed |
description | BACKGROUND: Genetic variation in HLA genes influence the immune response and may thus contribute to differential development of tuberculosis (TB) in HIV-infected individuals. The study was designed to determine whether HLA polymorphisms influence the development of Mycobacterium tuberculosis infection in HIV-infected individuals. MATERIALS AND METHODS: Fifty HIV-positive individuals without TB (HIV+TB−), 50 HIV patients co-infected with TB (HIV+TB+) and 50 control subjects (HIV-TB-) were analyzed for HLA Class I and II polymorphisms. RESULTS: In HLA Class II, frequency of occurrence of DRB1*13 (OR 3.165, CI 1.176–8.518, P value 0.019), DRB5 (OR 2.253, CI 1.011–5.019, P value 0.045) and DQB1*06 (OR 2.705, CI 1.197–6.113, P value 0.016) were increased in HIV+TB+compared to HIV+TB−. HLA DQB1*02 (OR 0.436, CI 0.185–1.029, P value 0.05) on the other hand conferred a protective role. In HLA Class I, frequency of B*15 (OR 2.705, CI 1.040–7.036, P value 0.038) was increased, whereas B*51 (OR 0.148, CI 0.031–0.706, P value 0.007) was decreased in HIV+TB+group compared to HIV+TB−. These differences however were not significant when compared with healthy controls. CONCLUSION: HLA polymorphisms independently did not account for the susceptibility to either of the disease mostly, although they seem to play a role once the infection(s) has established in a particular individual. Further studies are needed on a larger sample size to confirm these observations. |
format | Online Article Text |
id | pubmed-4586997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45869972015-12-01 Analysis of HLA association among North Indian HIV-positive individuals co-infected with Mycobacterium tuberculosis Saikia, Biman Wanchu, Ajay Mahakur, Sobhana Bind, Mahendra Sarkar, Krishnakali Minz, Ranjana W Lung India Original Article BACKGROUND: Genetic variation in HLA genes influence the immune response and may thus contribute to differential development of tuberculosis (TB) in HIV-infected individuals. The study was designed to determine whether HLA polymorphisms influence the development of Mycobacterium tuberculosis infection in HIV-infected individuals. MATERIALS AND METHODS: Fifty HIV-positive individuals without TB (HIV+TB−), 50 HIV patients co-infected with TB (HIV+TB+) and 50 control subjects (HIV-TB-) were analyzed for HLA Class I and II polymorphisms. RESULTS: In HLA Class II, frequency of occurrence of DRB1*13 (OR 3.165, CI 1.176–8.518, P value 0.019), DRB5 (OR 2.253, CI 1.011–5.019, P value 0.045) and DQB1*06 (OR 2.705, CI 1.197–6.113, P value 0.016) were increased in HIV+TB+compared to HIV+TB−. HLA DQB1*02 (OR 0.436, CI 0.185–1.029, P value 0.05) on the other hand conferred a protective role. In HLA Class I, frequency of B*15 (OR 2.705, CI 1.040–7.036, P value 0.038) was increased, whereas B*51 (OR 0.148, CI 0.031–0.706, P value 0.007) was decreased in HIV+TB+group compared to HIV+TB−. These differences however were not significant when compared with healthy controls. CONCLUSION: HLA polymorphisms independently did not account for the susceptibility to either of the disease mostly, although they seem to play a role once the infection(s) has established in a particular individual. Further studies are needed on a larger sample size to confirm these observations. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4586997/ /pubmed/26628757 http://dx.doi.org/10.4103/0970-2113.164166 Text en Copyright: © Lung India http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Saikia, Biman Wanchu, Ajay Mahakur, Sobhana Bind, Mahendra Sarkar, Krishnakali Minz, Ranjana W Analysis of HLA association among North Indian HIV-positive individuals co-infected with Mycobacterium tuberculosis |
title | Analysis of HLA association among North Indian HIV-positive individuals co-infected with Mycobacterium tuberculosis |
title_full | Analysis of HLA association among North Indian HIV-positive individuals co-infected with Mycobacterium tuberculosis |
title_fullStr | Analysis of HLA association among North Indian HIV-positive individuals co-infected with Mycobacterium tuberculosis |
title_full_unstemmed | Analysis of HLA association among North Indian HIV-positive individuals co-infected with Mycobacterium tuberculosis |
title_short | Analysis of HLA association among North Indian HIV-positive individuals co-infected with Mycobacterium tuberculosis |
title_sort | analysis of hla association among north indian hiv-positive individuals co-infected with mycobacterium tuberculosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586997/ https://www.ncbi.nlm.nih.gov/pubmed/26628757 http://dx.doi.org/10.4103/0970-2113.164166 |
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