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Development of a One-Step Probe Based Molecular Assay for Rapid Immunodiagnosis of Infection with M. tuberculosis Using Dried Blood Spots

BACKGROUND: Antigen specific release of IP-10 is the most promising alternative marker to IFN-γ for infection with M. tuberculosis. Compared to Interferon-γ release assays (IGRA), IP-10 is released in high levels enabling novel approaches such as field friendly dried blood spots (DBS) and molecular...

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Autores principales: Blauenfeldt, Thomas, Heyckendorf, Jan, Graff Jensen, Sidse, Lange, Christoph, Drabe, Camilla, Hermansen, Thomas S., de Thurah, Lena, Lillebaek, Troels, Eugen-Olsen, Jesper, Seersholm, Niels, Hoff, Søren, Bonde, Jesper, Ruhwald, Morten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153573/
https://www.ncbi.nlm.nih.gov/pubmed/25184553
http://dx.doi.org/10.1371/journal.pone.0105628
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author Blauenfeldt, Thomas
Heyckendorf, Jan
Graff Jensen, Sidse
Lange, Christoph
Drabe, Camilla
Hermansen, Thomas S.
de Thurah, Lena
Lillebaek, Troels
Eugen-Olsen, Jesper
Seersholm, Niels
Hoff, Søren
Bonde, Jesper
Ruhwald, Morten
author_facet Blauenfeldt, Thomas
Heyckendorf, Jan
Graff Jensen, Sidse
Lange, Christoph
Drabe, Camilla
Hermansen, Thomas S.
de Thurah, Lena
Lillebaek, Troels
Eugen-Olsen, Jesper
Seersholm, Niels
Hoff, Søren
Bonde, Jesper
Ruhwald, Morten
author_sort Blauenfeldt, Thomas
collection PubMed
description BACKGROUND: Antigen specific release of IP-10 is the most promising alternative marker to IFN-γ for infection with M. tuberculosis. Compared to Interferon-γ release assays (IGRA), IP-10 is released in high levels enabling novel approaches such as field friendly dried blood spots (DBS) and molecular detection. AIM: To develop a robust IP-10 based molecular assay for the diagnosis of infection with M. tubercuolsis from whole blood and DBS. METHOD: We developed a one-step probe based multiplex RT-qPCR assay for detecting IP-10 and IFN-γ mRNA expression from whole blood and DBS samples. The assay was validated and applied for the diagnosis of M. tuberculosis infection in DBS samples from 43 patients with confirmed TB, 13 patients with latent TB and 96 presumed uninfected controls. In parallel, IP-10 and INF-γ levels were measured in Quantiferon (QFT-TB) plasma supernatants. RESULTS: IP-10 mRNA upregulation was detectable at 4 hours after stimulation (6 fold upregulation) peaking at 8 hours (108 fold upregulation). IFN-γ expression occurred in concert but levels were lower (peak 6.7 fold upregulation). IP-10 gene expression level was significantly higher in patients with tuberculosis (median 31.2, IQR 10.7–67.0) and persons with latent tuberculosis infection (LTBI) (41.2, IQR 9.8–64.9) compared to healthy controls (1.6, IQR 1.1–2.4; p<0.0001). The IP-10 mRNA and protein based tests had comparable diagnostic accuracy to QFT-TB, sensitivity (85% and 88% vs 85%) and specificity (96% and 96% vs 97%, p = ns.). CONCLUSION: We developed a rapid, robust and accurate molecular immunodiagnostic test for M. tuberculosis infection. By combining DBS based sample acquisition, mail or currier based sample transport with centralized molecular detection, this immunodiagnostic test concept can reduce the local technological requirements everywhere and make it possible to offer highly accurate immunodiagnostic tests in low resource settings.
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spelling pubmed-41535732014-09-05 Development of a One-Step Probe Based Molecular Assay for Rapid Immunodiagnosis of Infection with M. tuberculosis Using Dried Blood Spots Blauenfeldt, Thomas Heyckendorf, Jan Graff Jensen, Sidse Lange, Christoph Drabe, Camilla Hermansen, Thomas S. de Thurah, Lena Lillebaek, Troels Eugen-Olsen, Jesper Seersholm, Niels Hoff, Søren Bonde, Jesper Ruhwald, Morten PLoS One Research Article BACKGROUND: Antigen specific release of IP-10 is the most promising alternative marker to IFN-γ for infection with M. tuberculosis. Compared to Interferon-γ release assays (IGRA), IP-10 is released in high levels enabling novel approaches such as field friendly dried blood spots (DBS) and molecular detection. AIM: To develop a robust IP-10 based molecular assay for the diagnosis of infection with M. tubercuolsis from whole blood and DBS. METHOD: We developed a one-step probe based multiplex RT-qPCR assay for detecting IP-10 and IFN-γ mRNA expression from whole blood and DBS samples. The assay was validated and applied for the diagnosis of M. tuberculosis infection in DBS samples from 43 patients with confirmed TB, 13 patients with latent TB and 96 presumed uninfected controls. In parallel, IP-10 and INF-γ levels were measured in Quantiferon (QFT-TB) plasma supernatants. RESULTS: IP-10 mRNA upregulation was detectable at 4 hours after stimulation (6 fold upregulation) peaking at 8 hours (108 fold upregulation). IFN-γ expression occurred in concert but levels were lower (peak 6.7 fold upregulation). IP-10 gene expression level was significantly higher in patients with tuberculosis (median 31.2, IQR 10.7–67.0) and persons with latent tuberculosis infection (LTBI) (41.2, IQR 9.8–64.9) compared to healthy controls (1.6, IQR 1.1–2.4; p<0.0001). The IP-10 mRNA and protein based tests had comparable diagnostic accuracy to QFT-TB, sensitivity (85% and 88% vs 85%) and specificity (96% and 96% vs 97%, p = ns.). CONCLUSION: We developed a rapid, robust and accurate molecular immunodiagnostic test for M. tuberculosis infection. By combining DBS based sample acquisition, mail or currier based sample transport with centralized molecular detection, this immunodiagnostic test concept can reduce the local technological requirements everywhere and make it possible to offer highly accurate immunodiagnostic tests in low resource settings. Public Library of Science 2014-09-03 /pmc/articles/PMC4153573/ /pubmed/25184553 http://dx.doi.org/10.1371/journal.pone.0105628 Text en © 2014 Blauenfeldt 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Blauenfeldt, Thomas
Heyckendorf, Jan
Graff Jensen, Sidse
Lange, Christoph
Drabe, Camilla
Hermansen, Thomas S.
de Thurah, Lena
Lillebaek, Troels
Eugen-Olsen, Jesper
Seersholm, Niels
Hoff, Søren
Bonde, Jesper
Ruhwald, Morten
Development of a One-Step Probe Based Molecular Assay for Rapid Immunodiagnosis of Infection with M. tuberculosis Using Dried Blood Spots
title Development of a One-Step Probe Based Molecular Assay for Rapid Immunodiagnosis of Infection with M. tuberculosis Using Dried Blood Spots
title_full Development of a One-Step Probe Based Molecular Assay for Rapid Immunodiagnosis of Infection with M. tuberculosis Using Dried Blood Spots
title_fullStr Development of a One-Step Probe Based Molecular Assay for Rapid Immunodiagnosis of Infection with M. tuberculosis Using Dried Blood Spots
title_full_unstemmed Development of a One-Step Probe Based Molecular Assay for Rapid Immunodiagnosis of Infection with M. tuberculosis Using Dried Blood Spots
title_short Development of a One-Step Probe Based Molecular Assay for Rapid Immunodiagnosis of Infection with M. tuberculosis Using Dried Blood Spots
title_sort development of a one-step probe based molecular assay for rapid immunodiagnosis of infection with m. tuberculosis using dried blood spots
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153573/
https://www.ncbi.nlm.nih.gov/pubmed/25184553
http://dx.doi.org/10.1371/journal.pone.0105628
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