Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ahmed, Mohamed I. M., Ziegler, Christian, Held, Kathrin, Dubinski, Ilja, Ley-Zaporozhan, Julia, Geldmacher, Christof, von Both, Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
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
_version_ 1783395898645020672
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
work_keys_str_mv AT ahmedmohamedim thetamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT zieglerchristian thetamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT heldkathrin thetamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT dubinskiilja thetamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT leyzaporozhanjulia thetamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT geldmacherchristof thetamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT vonbothulrich thetamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT ahmedmohamedim tamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT zieglerchristian tamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT heldkathrin tamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT dubinskiilja tamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT leyzaporozhanjulia tamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT geldmacherchristof tamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring
AT vonbothulrich tamtbassayapromisingtbimmunediagnostictestwithapotentialfortreatmentmonitoring