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The TAM-TB Assay—A Promising TB Immune-Diagnostic Test With a Potential for Treatment Monitoring
Tuberculosis (TB) epidemiology is changing in Western and Central Europe due to the rise in immigration and refugees fleeing high-TB-burden areas of war and devastation. The change in local demography and the lack of sensitive and specific TB diagnostic and monitoring tools, especially for cases of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378289/ https://www.ncbi.nlm.nih.gov/pubmed/30805325 http://dx.doi.org/10.3389/fped.2019.00027 |
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author | Ahmed, Mohamed I. M. Ziegler, Christian Held, Kathrin Dubinski, Ilja Ley-Zaporozhan, Julia Geldmacher, Christof von Both, Ulrich |
author_facet | Ahmed, Mohamed I. M. Ziegler, Christian Held, Kathrin Dubinski, Ilja Ley-Zaporozhan, Julia Geldmacher, Christof von Both, Ulrich |
author_sort | Ahmed, Mohamed I. M. |
collection | PubMed |
description | Tuberculosis (TB) epidemiology is changing in Western and Central Europe due to the rise in immigration and refugees fleeing high-TB-burden areas of war and devastation. The change in local demography and the lack of sensitive and specific TB diagnostic and monitoring tools, especially for cases of childhood TB, leads to either missed cases or over-treatment of this group. Here we present a promising new diagnostic approach, the T cell activation marker (TAM)-TB assay, and its performance in a case of extra-pulmonary TB occurring in a 16 year old refugee from Afghanistan. This assay is based on the characterization of 3 activation markers (CD38, HLA-DR, and Ki67) and one maturation marker (CD27) on M. tuberculosis-specific CD4 T cells. It was performed at time-points T0 (10 days), T1 (1 month), T2 (6 months), and T3 (12 months) post-treatment initiation. All markers were able to detect active tuberculosis (aTB) within this patient at T0 and reverted to a healthy/LTBI phenotype at the end of treatment. Tantalizingly, there was a clear trend toward the healthy/LTBI phenotype for the markers at T1 and T2, indicating a potential role in monitoring anti-TB treatment in the future. This assay may therefore contribute to improved TB diagnostic algorithms and TB treatment monitoring, potentially allowing for individualization of TB treatment duration in the future. |
format | Online Article Text |
id | pubmed-6378289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63782892019-02-25 The TAM-TB Assay—A Promising TB Immune-Diagnostic Test With a Potential for Treatment Monitoring Ahmed, Mohamed I. M. Ziegler, Christian Held, Kathrin Dubinski, Ilja Ley-Zaporozhan, Julia Geldmacher, Christof von Both, Ulrich Front Pediatr Pediatrics Tuberculosis (TB) epidemiology is changing in Western and Central Europe due to the rise in immigration and refugees fleeing high-TB-burden areas of war and devastation. The change in local demography and the lack of sensitive and specific TB diagnostic and monitoring tools, especially for cases of childhood TB, leads to either missed cases or over-treatment of this group. Here we present a promising new diagnostic approach, the T cell activation marker (TAM)-TB assay, and its performance in a case of extra-pulmonary TB occurring in a 16 year old refugee from Afghanistan. This assay is based on the characterization of 3 activation markers (CD38, HLA-DR, and Ki67) and one maturation marker (CD27) on M. tuberculosis-specific CD4 T cells. It was performed at time-points T0 (10 days), T1 (1 month), T2 (6 months), and T3 (12 months) post-treatment initiation. All markers were able to detect active tuberculosis (aTB) within this patient at T0 and reverted to a healthy/LTBI phenotype at the end of treatment. Tantalizingly, there was a clear trend toward the healthy/LTBI phenotype for the markers at T1 and T2, indicating a potential role in monitoring anti-TB treatment in the future. This assay may therefore contribute to improved TB diagnostic algorithms and TB treatment monitoring, potentially allowing for individualization of TB treatment duration in the future. Frontiers Media S.A. 2019-02-11 /pmc/articles/PMC6378289/ /pubmed/30805325 http://dx.doi.org/10.3389/fped.2019.00027 Text en Copyright © 2019 Ahmed, Ziegler, Held, Dubinski, Ley-Zaporozhan, Geldmacher and von Both. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics Ahmed, Mohamed I. M. Ziegler, Christian Held, Kathrin Dubinski, Ilja Ley-Zaporozhan, Julia Geldmacher, Christof von Both, Ulrich The TAM-TB Assay—A Promising TB Immune-Diagnostic Test With a Potential for Treatment Monitoring |
title | The TAM-TB Assay—A Promising TB Immune-Diagnostic Test With a Potential for Treatment Monitoring |
title_full | The TAM-TB Assay—A Promising TB Immune-Diagnostic Test With a Potential for Treatment Monitoring |
title_fullStr | The TAM-TB Assay—A Promising TB Immune-Diagnostic Test With a Potential for Treatment Monitoring |
title_full_unstemmed | The TAM-TB Assay—A Promising TB Immune-Diagnostic Test With a Potential for Treatment Monitoring |
title_short | The TAM-TB Assay—A Promising TB Immune-Diagnostic Test With a Potential for Treatment Monitoring |
title_sort | tam-tb assay—a promising tb immune-diagnostic test with a potential for treatment monitoring |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378289/ https://www.ncbi.nlm.nih.gov/pubmed/30805325 http://dx.doi.org/10.3389/fped.2019.00027 |
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