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Improving the coverage and accuracy of syphilis testing: The development of a novel rapid, point-of-care test for confirmatory testing of active syphilis infection and its early evaluation in China and South Africa

BACKGROUND: Current point-of-care tests (POCT) for syphilis, based on the detection of Treponema pallidum (TP) total antibodies, have limited capacity in distinguishing between active and past/treated syphilis. We report the development and early evaluation of a new prototype POCT based on the detec...

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Autores principales: Pham, Minh D., Wise, Amy, Garcia, Mary L., Van, Huy, Zheng, Shuning, Mohamed, Yasmin, Han, Yan, Wei, Wan-Hui, Yin, Yue-Ping, Chen, Xiang-Sheng, Dimech, Wayne, Braniff, Susie, Technau, Karl-Günter, Luchters, Stanley, Anderson, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327895/
https://www.ncbi.nlm.nih.gov/pubmed/32637904
http://dx.doi.org/10.1016/j.eclinm.2020.100440
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author Pham, Minh D.
Wise, Amy
Garcia, Mary L.
Van, Huy
Zheng, Shuning
Mohamed, Yasmin
Han, Yan
Wei, Wan-Hui
Yin, Yue-Ping
Chen, Xiang-Sheng
Dimech, Wayne
Braniff, Susie
Technau, Karl-Günter
Luchters, Stanley
Anderson, David A.
author_facet Pham, Minh D.
Wise, Amy
Garcia, Mary L.
Van, Huy
Zheng, Shuning
Mohamed, Yasmin
Han, Yan
Wei, Wan-Hui
Yin, Yue-Ping
Chen, Xiang-Sheng
Dimech, Wayne
Braniff, Susie
Technau, Karl-Günter
Luchters, Stanley
Anderson, David A.
author_sort Pham, Minh D.
collection PubMed
description BACKGROUND: Current point-of-care tests (POCT) for syphilis, based on the detection of Treponema pallidum (TP) total antibodies, have limited capacity in distinguishing between active and past/treated syphilis. We report the development and early evaluation of a new prototype POCT based on the detection of TP-IgA antibodies, a novel biomarker for active syphilis. METHODS: The TP-IgA POCT (index test) was developed in response to the World Health Organisation (WHO) target product profile (TPP) for a POCT for confirmatory syphilis testing. Two sub-studies were conducted consecutively using 458 pre-characterised stored plasma samples in China (sub-study one, addressing the criteria for the WHO TPP), and 503 venous blood samples collected from pregnant/postpartum women in South Africa (sub-study two, addressing potential clinical utility). Performance of the index test was assessed against standard laboratory-based serology using a combination of treponemal (TPHA) and non-treponemal (rapid plasma reagin [RPR]) tests. FINDINGS: In sub-study one, the index test demonstrated 96·1% (95%CI=91·7%-98·5%) sensitivity and 84·7% (95%CI=80·15–88·6%) specificity for identification of active syphilis (TPHA positive, RPR positive). It correctly identified 71% (107/150) samples of past-treated syphilis (TPHA positive, RPR negative). In sub-study two, the index test achieved 100% (95%CI=59%-100%) sensitivity for active syphilis and correctly identified all nine women with past syphilis. INTERPRETATION: The TP-IgA POCT has met the WHO TPP for a POCT for diagnosis of active syphilis and demonstrated its potential utility in a clinical setting. Future studies are warranted to evaluate field performance of the final manufactured test. FUNDING: Saving Lives at Birth: Grand Challenge for Development, Thrasher Research Fund, and the Victorian Government Operational Infrastructure Scheme.
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spelling pubmed-73278952020-07-06 Improving the coverage and accuracy of syphilis testing: The development of a novel rapid, point-of-care test for confirmatory testing of active syphilis infection and its early evaluation in China and South Africa Pham, Minh D. Wise, Amy Garcia, Mary L. Van, Huy Zheng, Shuning Mohamed, Yasmin Han, Yan Wei, Wan-Hui Yin, Yue-Ping Chen, Xiang-Sheng Dimech, Wayne Braniff, Susie Technau, Karl-Günter Luchters, Stanley Anderson, David A. EClinicalMedicine Research paper BACKGROUND: Current point-of-care tests (POCT) for syphilis, based on the detection of Treponema pallidum (TP) total antibodies, have limited capacity in distinguishing between active and past/treated syphilis. We report the development and early evaluation of a new prototype POCT based on the detection of TP-IgA antibodies, a novel biomarker for active syphilis. METHODS: The TP-IgA POCT (index test) was developed in response to the World Health Organisation (WHO) target product profile (TPP) for a POCT for confirmatory syphilis testing. Two sub-studies were conducted consecutively using 458 pre-characterised stored plasma samples in China (sub-study one, addressing the criteria for the WHO TPP), and 503 venous blood samples collected from pregnant/postpartum women in South Africa (sub-study two, addressing potential clinical utility). Performance of the index test was assessed against standard laboratory-based serology using a combination of treponemal (TPHA) and non-treponemal (rapid plasma reagin [RPR]) tests. FINDINGS: In sub-study one, the index test demonstrated 96·1% (95%CI=91·7%-98·5%) sensitivity and 84·7% (95%CI=80·15–88·6%) specificity for identification of active syphilis (TPHA positive, RPR positive). It correctly identified 71% (107/150) samples of past-treated syphilis (TPHA positive, RPR negative). In sub-study two, the index test achieved 100% (95%CI=59%-100%) sensitivity for active syphilis and correctly identified all nine women with past syphilis. INTERPRETATION: The TP-IgA POCT has met the WHO TPP for a POCT for diagnosis of active syphilis and demonstrated its potential utility in a clinical setting. Future studies are warranted to evaluate field performance of the final manufactured test. FUNDING: Saving Lives at Birth: Grand Challenge for Development, Thrasher Research Fund, and the Victorian Government Operational Infrastructure Scheme. Elsevier 2020-06-27 /pmc/articles/PMC7327895/ /pubmed/32637904 http://dx.doi.org/10.1016/j.eclinm.2020.100440 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research paper
Pham, Minh D.
Wise, Amy
Garcia, Mary L.
Van, Huy
Zheng, Shuning
Mohamed, Yasmin
Han, Yan
Wei, Wan-Hui
Yin, Yue-Ping
Chen, Xiang-Sheng
Dimech, Wayne
Braniff, Susie
Technau, Karl-Günter
Luchters, Stanley
Anderson, David A.
Improving the coverage and accuracy of syphilis testing: The development of a novel rapid, point-of-care test for confirmatory testing of active syphilis infection and its early evaluation in China and South Africa
title Improving the coverage and accuracy of syphilis testing: The development of a novel rapid, point-of-care test for confirmatory testing of active syphilis infection and its early evaluation in China and South Africa
title_full Improving the coverage and accuracy of syphilis testing: The development of a novel rapid, point-of-care test for confirmatory testing of active syphilis infection and its early evaluation in China and South Africa
title_fullStr Improving the coverage and accuracy of syphilis testing: The development of a novel rapid, point-of-care test for confirmatory testing of active syphilis infection and its early evaluation in China and South Africa
title_full_unstemmed Improving the coverage and accuracy of syphilis testing: The development of a novel rapid, point-of-care test for confirmatory testing of active syphilis infection and its early evaluation in China and South Africa
title_short Improving the coverage and accuracy of syphilis testing: The development of a novel rapid, point-of-care test for confirmatory testing of active syphilis infection and its early evaluation in China and South Africa
title_sort improving the coverage and accuracy of syphilis testing: the development of a novel rapid, point-of-care test for confirmatory testing of active syphilis infection and its early evaluation in china and south africa
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327895/
https://www.ncbi.nlm.nih.gov/pubmed/32637904
http://dx.doi.org/10.1016/j.eclinm.2020.100440
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