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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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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. |
format | Online Article Text |
id | pubmed-5687722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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