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Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell function

The WHO estimates around a million children contract tuberculosis (TB) annually with over 80 000 deaths from dissemination of infection outside of the lungs. The insidious onset and association with skin test anergy suggests failure of the immune system to both recognise and respond to infection. To...

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Autores principales: Hemingway, Cheryl, Berk, Maurice, Anderson, Suzanne T., Wright, Victoria J., Hamilton, Shea, Eleftherohorinou, Hariklia, Kaforou, Myrsini, Goldgof, Greg M., Hickman, Katy, Kampmann, Beate, Schoeman, Johan, Eley, Brian, Beatty, David, Pienaar, Sandra, Nicol, Mark P., Griffiths, Michael J., Waddell, Simon J., Newton, Sandra M., Coin, Lachlan J., Relman, David A., Montana, Giovanni, Levin, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687722/
https://www.ncbi.nlm.nih.gov/pubmed/29140996
http://dx.doi.org/10.1371/journal.pone.0185973
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author Hemingway, Cheryl
Berk, Maurice
Anderson, Suzanne T.
Wright, Victoria J.
Hamilton, Shea
Eleftherohorinou, Hariklia
Kaforou, Myrsini
Goldgof, Greg M.
Hickman, Katy
Kampmann, Beate
Schoeman, Johan
Eley, Brian
Beatty, David
Pienaar, Sandra
Nicol, Mark P.
Griffiths, Michael J.
Waddell, Simon J.
Newton, Sandra M.
Coin, Lachlan J.
Relman, David A.
Montana, Giovanni
Levin, Michael
author_facet Hemingway, Cheryl
Berk, Maurice
Anderson, Suzanne T.
Wright, Victoria J.
Hamilton, Shea
Eleftherohorinou, Hariklia
Kaforou, Myrsini
Goldgof, Greg M.
Hickman, Katy
Kampmann, Beate
Schoeman, Johan
Eley, Brian
Beatty, David
Pienaar, Sandra
Nicol, Mark P.
Griffiths, Michael J.
Waddell, Simon J.
Newton, Sandra M.
Coin, Lachlan J.
Relman, David A.
Montana, Giovanni
Levin, Michael
author_sort Hemingway, Cheryl
collection PubMed
description The WHO estimates around a million children contract tuberculosis (TB) annually with over 80 000 deaths from dissemination of infection outside of the lungs. The insidious onset and association with skin test anergy suggests failure of the immune system to both recognise and respond to infection. To understand the immune mechanisms, we studied genome-wide whole blood RNA expression in children with TB meningitis (TBM). Findings were validated in a second cohort of children with TBM and pulmonary TB (PTB), and functional T-cell responses studied in a third cohort of children with TBM, other extrapulmonary TB (EPTB) and PTB. The predominant RNA transcriptional response in children with TBM was decreased abundance of multiple genes, with 140/204 (68%) of all differentially regulated genes showing reduced abundance compared to healthy controls. Findings were validated in a second cohort with concordance of the direction of differential expression in both TBM (r(2) = 0.78 p = 2x10(-16)) and PTB patients (r(2) = 0.71 p = 2x10(-16)) when compared to a second group of healthy controls. Although the direction of expression of these significant genes was similar in the PTB patients, the magnitude of differential transcript abundance was less in PTB than in TBM. The majority of genes were involved in activation of leucocytes (p = 2.67E(-11)) and T-cell receptor signalling (p = 6.56E(-07)). Less abundant gene expression in immune cells was associated with a functional defect in T-cell proliferation that recovered after full TB treatment (p<0.0003). Multiple genes involved in T-cell activation show decreased abundance in children with acute TB, who also have impaired functional T-cell responses. Our data suggest that childhood TB is associated with an acquired immune defect, potentially resulting in failure to contain the pathogen. Elucidation of the mechanism causing the immune paresis may identify new treatment and prevention strategies.
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spelling pubmed-56877222017-11-30 Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell function Hemingway, Cheryl Berk, Maurice Anderson, Suzanne T. Wright, Victoria J. Hamilton, Shea Eleftherohorinou, Hariklia Kaforou, Myrsini Goldgof, Greg M. Hickman, Katy Kampmann, Beate Schoeman, Johan Eley, Brian Beatty, David Pienaar, Sandra Nicol, Mark P. Griffiths, Michael J. Waddell, Simon J. Newton, Sandra M. Coin, Lachlan J. Relman, David A. Montana, Giovanni Levin, Michael PLoS One Research Article The WHO estimates around a million children contract tuberculosis (TB) annually with over 80 000 deaths from dissemination of infection outside of the lungs. The insidious onset and association with skin test anergy suggests failure of the immune system to both recognise and respond to infection. To understand the immune mechanisms, we studied genome-wide whole blood RNA expression in children with TB meningitis (TBM). Findings were validated in a second cohort of children with TBM and pulmonary TB (PTB), and functional T-cell responses studied in a third cohort of children with TBM, other extrapulmonary TB (EPTB) and PTB. The predominant RNA transcriptional response in children with TBM was decreased abundance of multiple genes, with 140/204 (68%) of all differentially regulated genes showing reduced abundance compared to healthy controls. Findings were validated in a second cohort with concordance of the direction of differential expression in both TBM (r(2) = 0.78 p = 2x10(-16)) and PTB patients (r(2) = 0.71 p = 2x10(-16)) when compared to a second group of healthy controls. Although the direction of expression of these significant genes was similar in the PTB patients, the magnitude of differential transcript abundance was less in PTB than in TBM. The majority of genes were involved in activation of leucocytes (p = 2.67E(-11)) and T-cell receptor signalling (p = 6.56E(-07)). Less abundant gene expression in immune cells was associated with a functional defect in T-cell proliferation that recovered after full TB treatment (p<0.0003). Multiple genes involved in T-cell activation show decreased abundance in children with acute TB, who also have impaired functional T-cell responses. Our data suggest that childhood TB is associated with an acquired immune defect, potentially resulting in failure to contain the pathogen. Elucidation of the mechanism causing the immune paresis may identify new treatment and prevention strategies. Public Library of Science 2017-11-15 /pmc/articles/PMC5687722/ /pubmed/29140996 http://dx.doi.org/10.1371/journal.pone.0185973 Text en © 2017 Hemingway 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hemingway, Cheryl
Berk, Maurice
Anderson, Suzanne T.
Wright, Victoria J.
Hamilton, Shea
Eleftherohorinou, Hariklia
Kaforou, Myrsini
Goldgof, Greg M.
Hickman, Katy
Kampmann, Beate
Schoeman, Johan
Eley, Brian
Beatty, David
Pienaar, Sandra
Nicol, Mark P.
Griffiths, Michael J.
Waddell, Simon J.
Newton, Sandra M.
Coin, Lachlan J.
Relman, David A.
Montana, Giovanni
Levin, Michael
Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell function
title Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell function
title_full Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell function
title_fullStr Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell function
title_full_unstemmed Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell function
title_short Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell function
title_sort childhood tuberculosis is associated with decreased abundance of t cell gene transcripts and impaired t cell function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687722/
https://www.ncbi.nlm.nih.gov/pubmed/29140996
http://dx.doi.org/10.1371/journal.pone.0185973
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