Field-friendly serological tests for determination of M. leprae-specific antibodies

Abstract Early detection of leprosy is key to reduce the ongoing transmission. Antibodies directed against M. leprae PGL-I represent a useful biomarker for detecting multibacillary (MB) patients. Since efficient leprosy diagnosis requires field-friendly test conditions, we evaluated two rapid latera...

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Autores principales: Anouk van Hooij, Elisa M. Tjon Kon Fat, Susan J. F. van den Eeden, Louis Wilson, Moises Batista da Silva, Claudio G. Salgado, John S. Spencer, Paul L. A. M. Corstjens, Annemieke Geluk
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Publicado: Nature Portfolio 2017
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spelling oai:doaj.org-article:f2a8a590d48c4ec883a2189ae5b3d5ef2021-12-02T15:18:52ZField-friendly serological tests for determination of M. leprae-specific antibodies10.1038/s41598-017-07803-72045-2322https://doaj.org/article/f2a8a590d48c4ec883a2189ae5b3d5ef2017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-07803-7https://doaj.org/toc/2045-2322Abstract Early detection of leprosy is key to reduce the ongoing transmission. Antibodies directed against M. leprae PGL-I represent a useful biomarker for detecting multibacillary (MB) patients. Since efficient leprosy diagnosis requires field-friendly test conditions, we evaluated two rapid lateral flow assays (LFA) for detection of Mycobacterium leprae-specific antibodies: the visual immunogold OnSite Leprosy Ab Rapid test [Gold-LFA] and the quantitative, luminescent up-converting phosphor anti-PGL-I test [UCP-LFA]. Test performance was assessed in independent cohorts originating from three endemic areas. In the Philippine cohort comprising patients with high bacillary indices (BI; average:4,9), 94%(n = 161) of MB patients were identified by UCP-LFA and 78%(n = 133) by Gold-LFA. In the Bangladeshi cohort, including mainly MB patients with low BI (average:1), 41%(n = 14) and 44%(n = 15) were detected by UCP-LFA and Gold-LFA, respectively. In the third cohort of schoolchildren from a leprosy hyperendemic region in Brazil, both tests detected 28%(n = 17) seropositivity. Both rapid tests corresponded well with BI(p < 0.0001), with a fairly higher sensitivity obtained with the UCP-LFA assay. However, due to the spectral character of leprosy, additional, cellular biomarkers are required to detect patients with low BIs. Therefore, the UCP-LFA platform, which allows multiplexing with differential biomarkers, offers more cutting-edge potential for diagnosis across the whole leprosy spectrum.Anouk van HooijElisa M. Tjon Kon FatSusan J. F. van den EedenLouis WilsonMoises Batista da SilvaClaudio G. SalgadoJohn S. SpencerPaul L. A. M. CorstjensAnnemieke GelukNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Anouk van Hooij
Elisa M. Tjon Kon Fat
Susan J. F. van den Eeden
Louis Wilson
Moises Batista da Silva
Claudio G. Salgado
John S. Spencer
Paul L. A. M. Corstjens
Annemieke Geluk
Field-friendly serological tests for determination of M. leprae-specific antibodies
description Abstract Early detection of leprosy is key to reduce the ongoing transmission. Antibodies directed against M. leprae PGL-I represent a useful biomarker for detecting multibacillary (MB) patients. Since efficient leprosy diagnosis requires field-friendly test conditions, we evaluated two rapid lateral flow assays (LFA) for detection of Mycobacterium leprae-specific antibodies: the visual immunogold OnSite Leprosy Ab Rapid test [Gold-LFA] and the quantitative, luminescent up-converting phosphor anti-PGL-I test [UCP-LFA]. Test performance was assessed in independent cohorts originating from three endemic areas. In the Philippine cohort comprising patients with high bacillary indices (BI; average:4,9), 94%(n = 161) of MB patients were identified by UCP-LFA and 78%(n = 133) by Gold-LFA. In the Bangladeshi cohort, including mainly MB patients with low BI (average:1), 41%(n = 14) and 44%(n = 15) were detected by UCP-LFA and Gold-LFA, respectively. In the third cohort of schoolchildren from a leprosy hyperendemic region in Brazil, both tests detected 28%(n = 17) seropositivity. Both rapid tests corresponded well with BI(p < 0.0001), with a fairly higher sensitivity obtained with the UCP-LFA assay. However, due to the spectral character of leprosy, additional, cellular biomarkers are required to detect patients with low BIs. Therefore, the UCP-LFA platform, which allows multiplexing with differential biomarkers, offers more cutting-edge potential for diagnosis across the whole leprosy spectrum.
format article
author Anouk van Hooij
Elisa M. Tjon Kon Fat
Susan J. F. van den Eeden
Louis Wilson
Moises Batista da Silva
Claudio G. Salgado
John S. Spencer
Paul L. A. M. Corstjens
Annemieke Geluk
author_facet Anouk van Hooij
Elisa M. Tjon Kon Fat
Susan J. F. van den Eeden
Louis Wilson
Moises Batista da Silva
Claudio G. Salgado
John S. Spencer
Paul L. A. M. Corstjens
Annemieke Geluk
author_sort Anouk van Hooij
title Field-friendly serological tests for determination of M. leprae-specific antibodies
title_short Field-friendly serological tests for determination of M. leprae-specific antibodies
title_full Field-friendly serological tests for determination of M. leprae-specific antibodies
title_fullStr Field-friendly serological tests for determination of M. leprae-specific antibodies
title_full_unstemmed Field-friendly serological tests for determination of M. leprae-specific antibodies
title_sort field-friendly serological tests for determination of m. leprae-specific antibodies
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/f2a8a590d48c4ec883a2189ae5b3d5ef
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