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Humoral response to HspX and GlcB to previous and recent infection by Mycobacterium tuberculosis

BACKGROUND: Tuberculosis (TB) remains a major world health problem. Around 2 billions of people are infected by Mycobacterium tuberculosis, the causal agent of this disease. This fact accounts for a third of the total world population and it is expected that 9 million people will become infected eac...

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Autores principales: Rabahi, Marcelo Fouad, Junqueira-Kipnis, Ana Paula, dos Reis, Michelle Cristina Guerreiro, Oelemann, Walter, Conde, Marcus Barreto
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241823/
https://www.ncbi.nlm.nih.gov/pubmed/18166139
http://dx.doi.org/10.1186/1471-2334-7-148
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author Rabahi, Marcelo Fouad
Junqueira-Kipnis, Ana Paula
dos Reis, Michelle Cristina Guerreiro
Oelemann, Walter
Conde, Marcus Barreto
author_facet Rabahi, Marcelo Fouad
Junqueira-Kipnis, Ana Paula
dos Reis, Michelle Cristina Guerreiro
Oelemann, Walter
Conde, Marcus Barreto
author_sort Rabahi, Marcelo Fouad
collection PubMed
description BACKGROUND: Tuberculosis (TB) remains a major world health problem. Around 2 billions of people are infected by Mycobacterium tuberculosis, the causal agent of this disease. This fact accounts for a third of the total world population and it is expected that 9 million people will become infected each year. Only approximately 10% of the infected people will develop disease. However, health care workers (HCW) are continually exposed to the bacilli at endemic sites presenting increased chance of becoming sick. The objective of this work was to identify LTBI (latent tuberculosis infection) among all asymptomatic HCW of a Brazilian Central Hospital, in a three year follow up, and evaluate the humoral response among HCW with previous and recent LTBI to recombinant HspX and GlcB from M. tuberculosis. METHODS: Four hundred and thirty seven HCW were screened and classified into three different groups according to tuberculin skin test (TST) status: uninfected, previous LTBI and recent LTBI. ELISA test were performed to determine the humoral immune response to HspX and GlcB. RESULTS: The levels of IgG and IgM against the HspX and GlcB antigens were the same among HCW with recent and previous LTBI, as well as among non infected HCW. However, the IgM levels to HspX was significantly higher among HCW with recent LTBI (OD = 1.52 ± 0.40) than among the uninfected (OD = 1.09 ± 0.50) or subjects with previous LTBI (OD = 0.96 ± 0.51) (p < 0.001). CONCLUSION: IgG and IgM humoral responses to GlcB antigens were similar amongst all studied groups; nevertheless IgM levels against HspX were higher among the recent LTBI/HCW.
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spelling pubmed-22418232008-02-14 Humoral response to HspX and GlcB to previous and recent infection by Mycobacterium tuberculosis Rabahi, Marcelo Fouad Junqueira-Kipnis, Ana Paula dos Reis, Michelle Cristina Guerreiro Oelemann, Walter Conde, Marcus Barreto BMC Infect Dis Research Article BACKGROUND: Tuberculosis (TB) remains a major world health problem. Around 2 billions of people are infected by Mycobacterium tuberculosis, the causal agent of this disease. This fact accounts for a third of the total world population and it is expected that 9 million people will become infected each year. Only approximately 10% of the infected people will develop disease. However, health care workers (HCW) are continually exposed to the bacilli at endemic sites presenting increased chance of becoming sick. The objective of this work was to identify LTBI (latent tuberculosis infection) among all asymptomatic HCW of a Brazilian Central Hospital, in a three year follow up, and evaluate the humoral response among HCW with previous and recent LTBI to recombinant HspX and GlcB from M. tuberculosis. METHODS: Four hundred and thirty seven HCW were screened and classified into three different groups according to tuberculin skin test (TST) status: uninfected, previous LTBI and recent LTBI. ELISA test were performed to determine the humoral immune response to HspX and GlcB. RESULTS: The levels of IgG and IgM against the HspX and GlcB antigens were the same among HCW with recent and previous LTBI, as well as among non infected HCW. However, the IgM levels to HspX was significantly higher among HCW with recent LTBI (OD = 1.52 ± 0.40) than among the uninfected (OD = 1.09 ± 0.50) or subjects with previous LTBI (OD = 0.96 ± 0.51) (p < 0.001). CONCLUSION: IgG and IgM humoral responses to GlcB antigens were similar amongst all studied groups; nevertheless IgM levels against HspX were higher among the recent LTBI/HCW. BioMed Central 2007-12-31 /pmc/articles/PMC2241823/ /pubmed/18166139 http://dx.doi.org/10.1186/1471-2334-7-148 Text en Copyright © 2007 Rabahi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rabahi, Marcelo Fouad
Junqueira-Kipnis, Ana Paula
dos Reis, Michelle Cristina Guerreiro
Oelemann, Walter
Conde, Marcus Barreto
Humoral response to HspX and GlcB to previous and recent infection by Mycobacterium tuberculosis
title Humoral response to HspX and GlcB to previous and recent infection by Mycobacterium tuberculosis
title_full Humoral response to HspX and GlcB to previous and recent infection by Mycobacterium tuberculosis
title_fullStr Humoral response to HspX and GlcB to previous and recent infection by Mycobacterium tuberculosis
title_full_unstemmed Humoral response to HspX and GlcB to previous and recent infection by Mycobacterium tuberculosis
title_short Humoral response to HspX and GlcB to previous and recent infection by Mycobacterium tuberculosis
title_sort humoral response to hspx and glcb to previous and recent infection by mycobacterium tuberculosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241823/
https://www.ncbi.nlm.nih.gov/pubmed/18166139
http://dx.doi.org/10.1186/1471-2334-7-148
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