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Host markers in Quantiferon supernatants differentiate active TB from latent TB infection: preliminary report

BACKGROUND: Interferon gamma release assays, including the QuantiFERON(® )TB Gold In Tube (QFT) have been shown to be accurate in diagnosing Mycobacterium tuberculosis infection. These assays however, do not discriminate between latent TB infection (LTBI) and active TB disease. METHODS: We recruited...

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Autores principales: Chegou, Novel N, Black, Gillian F, Kidd, Martin, van Helden, Paul D, Walzl, Gerhard
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696407/
https://www.ncbi.nlm.nih.gov/pubmed/19445695
http://dx.doi.org/10.1186/1471-2466-9-21
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author Chegou, Novel N
Black, Gillian F
Kidd, Martin
van Helden, Paul D
Walzl, Gerhard
author_facet Chegou, Novel N
Black, Gillian F
Kidd, Martin
van Helden, Paul D
Walzl, Gerhard
author_sort Chegou, Novel N
collection PubMed
description BACKGROUND: Interferon gamma release assays, including the QuantiFERON(® )TB Gold In Tube (QFT) have been shown to be accurate in diagnosing Mycobacterium tuberculosis infection. These assays however, do not discriminate between latent TB infection (LTBI) and active TB disease. METHODS: We recruited twenty-three pulmonary TB patients and 34 household contacts from Cape Town, South Africa and performed the QFT test. To investigate the ability of new host markers to differentiate between LTBI and active TB, levels of 29 biomarkers in QFT supernatants were evaluated using a Luminex multiplex cytokine assay. RESULTS: Eight out of 29 biomarkers distinguished active TB from LTBI in a pilot study. Baseline levels of epidermal growth factor (EGF) soluble CD40 ligand (sCD40L), antigen stimulated levels of EGF, and the background corrected antigen stimulated levels of EGF and macrophage inflammatory protein (MIP)-1β were the most informative single markers for differentiation between TB disease and LTBI, with AUCs of 0.88, 0.84, 0.87, 0.90 and 0.79 respectively. The combination of EGF and MIP-1β predicted 96% of active TB cases and 92% of LTBIs. Combinations between EGF, sCD40L, VEGF, TGF-α and IL-1α also showed potential to differentiate between TB infection states. EGF, VEGF, TGF-α and sCD40L levels were higher in TB patients. CONCLUSION: These preliminary data suggest that active TB may be accurately differentiated from LTBI utilizing adaptations of the commercial QFT test that includes measurement of EGF, sCD40L, MIP-1β, VEGF, TGF-α or IL-1α in supernatants from QFT assays. This approach holds promise for development as a rapid diagnostic test for active TB.
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spelling pubmed-26964072009-06-16 Host markers in Quantiferon supernatants differentiate active TB from latent TB infection: preliminary report Chegou, Novel N Black, Gillian F Kidd, Martin van Helden, Paul D Walzl, Gerhard BMC Pulm Med Research Article BACKGROUND: Interferon gamma release assays, including the QuantiFERON(® )TB Gold In Tube (QFT) have been shown to be accurate in diagnosing Mycobacterium tuberculosis infection. These assays however, do not discriminate between latent TB infection (LTBI) and active TB disease. METHODS: We recruited twenty-three pulmonary TB patients and 34 household contacts from Cape Town, South Africa and performed the QFT test. To investigate the ability of new host markers to differentiate between LTBI and active TB, levels of 29 biomarkers in QFT supernatants were evaluated using a Luminex multiplex cytokine assay. RESULTS: Eight out of 29 biomarkers distinguished active TB from LTBI in a pilot study. Baseline levels of epidermal growth factor (EGF) soluble CD40 ligand (sCD40L), antigen stimulated levels of EGF, and the background corrected antigen stimulated levels of EGF and macrophage inflammatory protein (MIP)-1β were the most informative single markers for differentiation between TB disease and LTBI, with AUCs of 0.88, 0.84, 0.87, 0.90 and 0.79 respectively. The combination of EGF and MIP-1β predicted 96% of active TB cases and 92% of LTBIs. Combinations between EGF, sCD40L, VEGF, TGF-α and IL-1α also showed potential to differentiate between TB infection states. EGF, VEGF, TGF-α and sCD40L levels were higher in TB patients. CONCLUSION: These preliminary data suggest that active TB may be accurately differentiated from LTBI utilizing adaptations of the commercial QFT test that includes measurement of EGF, sCD40L, MIP-1β, VEGF, TGF-α or IL-1α in supernatants from QFT assays. This approach holds promise for development as a rapid diagnostic test for active TB. BioMed Central 2009-05-16 /pmc/articles/PMC2696407/ /pubmed/19445695 http://dx.doi.org/10.1186/1471-2466-9-21 Text en Copyright © 2009 Chegou et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chegou, Novel N
Black, Gillian F
Kidd, Martin
van Helden, Paul D
Walzl, Gerhard
Host markers in Quantiferon supernatants differentiate active TB from latent TB infection: preliminary report
title Host markers in Quantiferon supernatants differentiate active TB from latent TB infection: preliminary report
title_full Host markers in Quantiferon supernatants differentiate active TB from latent TB infection: preliminary report
title_fullStr Host markers in Quantiferon supernatants differentiate active TB from latent TB infection: preliminary report
title_full_unstemmed Host markers in Quantiferon supernatants differentiate active TB from latent TB infection: preliminary report
title_short Host markers in Quantiferon supernatants differentiate active TB from latent TB infection: preliminary report
title_sort host markers in quantiferon supernatants differentiate active tb from latent tb infection: preliminary report
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696407/
https://www.ncbi.nlm.nih.gov/pubmed/19445695
http://dx.doi.org/10.1186/1471-2466-9-21
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