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Inflammatory and immunogenetic markers in correlation with pulmonary tuberculosis
OBJECTIVE: To describe serum levels of the cytokines IL-10, TNF-α, and IFN-γ, as well as polymorphisms in the genes involved in their transcription, and their association with markers of the acute inflammatory response in patients with pulmonary tuberculosis. METHODS: This was a descriptive, longitu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Pneumologia e Tisiologia
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075896/ https://www.ncbi.nlm.nih.gov/pubmed/24473766 http://dx.doi.org/10.1590/S1806-37132013000600011 |
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author | Muller, Beatriz Lima Alezio Ramalho, Daniela Maria de Paula dos Santos, Paula Fernanda Gonçalves Mesquita, Eliene Denites Duarte Kritski, Afranio Lineu Oliveira, Martha Maria |
author_facet | Muller, Beatriz Lima Alezio Ramalho, Daniela Maria de Paula dos Santos, Paula Fernanda Gonçalves Mesquita, Eliene Denites Duarte Kritski, Afranio Lineu Oliveira, Martha Maria |
author_sort | Muller, Beatriz Lima Alezio |
collection | PubMed |
description | OBJECTIVE: To describe serum levels of the cytokines IL-10, TNF-α, and IFN-γ, as well as polymorphisms in the genes involved in their transcription, and their association with markers of the acute inflammatory response in patients with pulmonary tuberculosis. METHODS: This was a descriptive, longitudinal study involving 81 patients with pulmonary tuberculosis treated at two referral hospitals. We collected data on sociodemographic variables and evaluated bacteriological conversion at the eighth week of antituberculosis treatment, gene polymorphisms related to the cytokines studied, and serum levels of those cytokines, as well as those of C-reactive protein (CRP). We also determined the ESR and CD4+ counts. RESULTS: The median age of the patients was 43 years; 67 patients (82.7%) were male; and 8 patients (9.9%) were infected with HIV. The ESR was highest in the patients with high IFN-γ levels and low IL-10 levels. IFN-γ and TNF-α gene polymorphisms at positions +874 and −238, respectively, showed no correlations with the corresponding cytokine serum levels. Low IL-10 levels were associated with IL-10 gene polymorphisms at positions −592 and −819 (but not −1082). There was a negative association between bacteriological conversion at the eighth week of treatment and CRP levels. CONCLUSIONS: Our results suggest that genetic markers and markers of acute inflammatory response are useful in predicting the response to antituberculosis treatment. |
format | Online Article Text |
id | pubmed-4075896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Sociedade Brasileira de Pneumologia e Tisiologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-40758962014-07-16 Inflammatory and immunogenetic markers in correlation with pulmonary tuberculosis Muller, Beatriz Lima Alezio Ramalho, Daniela Maria de Paula dos Santos, Paula Fernanda Gonçalves Mesquita, Eliene Denites Duarte Kritski, Afranio Lineu Oliveira, Martha Maria J Bras Pneumol Original Articles OBJECTIVE: To describe serum levels of the cytokines IL-10, TNF-α, and IFN-γ, as well as polymorphisms in the genes involved in their transcription, and their association with markers of the acute inflammatory response in patients with pulmonary tuberculosis. METHODS: This was a descriptive, longitudinal study involving 81 patients with pulmonary tuberculosis treated at two referral hospitals. We collected data on sociodemographic variables and evaluated bacteriological conversion at the eighth week of antituberculosis treatment, gene polymorphisms related to the cytokines studied, and serum levels of those cytokines, as well as those of C-reactive protein (CRP). We also determined the ESR and CD4+ counts. RESULTS: The median age of the patients was 43 years; 67 patients (82.7%) were male; and 8 patients (9.9%) were infected with HIV. The ESR was highest in the patients with high IFN-γ levels and low IL-10 levels. IFN-γ and TNF-α gene polymorphisms at positions +874 and −238, respectively, showed no correlations with the corresponding cytokine serum levels. Low IL-10 levels were associated with IL-10 gene polymorphisms at positions −592 and −819 (but not −1082). There was a negative association between bacteriological conversion at the eighth week of treatment and CRP levels. CONCLUSIONS: Our results suggest that genetic markers and markers of acute inflammatory response are useful in predicting the response to antituberculosis treatment. Sociedade Brasileira de Pneumologia e Tisiologia 2013 /pmc/articles/PMC4075896/ /pubmed/24473766 http://dx.doi.org/10.1590/S1806-37132013000600011 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Muller, Beatriz Lima Alezio Ramalho, Daniela Maria de Paula dos Santos, Paula Fernanda Gonçalves Mesquita, Eliene Denites Duarte Kritski, Afranio Lineu Oliveira, Martha Maria Inflammatory and immunogenetic markers in correlation with pulmonary tuberculosis |
title | Inflammatory and immunogenetic markers in correlation
with pulmonary tuberculosis |
title_full | Inflammatory and immunogenetic markers in correlation
with pulmonary tuberculosis |
title_fullStr | Inflammatory and immunogenetic markers in correlation
with pulmonary tuberculosis |
title_full_unstemmed | Inflammatory and immunogenetic markers in correlation
with pulmonary tuberculosis |
title_short | Inflammatory and immunogenetic markers in correlation
with pulmonary tuberculosis |
title_sort | inflammatory and immunogenetic markers in correlation
with pulmonary tuberculosis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075896/ https://www.ncbi.nlm.nih.gov/pubmed/24473766 http://dx.doi.org/10.1590/S1806-37132013000600011 |
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