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Study roadmap for high-throughput development of easy to use and affordable biomarkers as diagnostics for tropical diseases: a focus on malaria and schistosomiasis

BACKGROUND: Interventions are currently being used against ‘infectious diseases of poverty’, which remain highly debilitating and deadly in most endemic countries, especially malaria, schistosomiasis, echinococcosis and African sleeping sickness. However, major limitations of current ‘traditional’ m...

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Autores principales: Kassegne, Kokouvi, Zhang, Ting, Chen, Shen-Bo, Xu, Bin, Dang, Zhi-Sheng, Deng, Wang-Ping, Abe, Eniola Michael, Shen, Hai-Mo, Hu, Wei, Guyo, Takele Geressu, Nwaka, Solomon, Chen, Jun-Hu, Zhou, Xiao-Nong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623970/
https://www.ncbi.nlm.nih.gov/pubmed/28965490
http://dx.doi.org/10.1186/s40249-017-0344-9
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author Kassegne, Kokouvi
Zhang, Ting
Chen, Shen-Bo
Xu, Bin
Dang, Zhi-Sheng
Deng, Wang-Ping
Abe, Eniola Michael
Shen, Hai-Mo
Hu, Wei
Guyo, Takele Geressu
Nwaka, Solomon
Chen, Jun-Hu
Zhou, Xiao-Nong
author_facet Kassegne, Kokouvi
Zhang, Ting
Chen, Shen-Bo
Xu, Bin
Dang, Zhi-Sheng
Deng, Wang-Ping
Abe, Eniola Michael
Shen, Hai-Mo
Hu, Wei
Guyo, Takele Geressu
Nwaka, Solomon
Chen, Jun-Hu
Zhou, Xiao-Nong
author_sort Kassegne, Kokouvi
collection PubMed
description BACKGROUND: Interventions are currently being used against ‘infectious diseases of poverty’, which remain highly debilitating and deadly in most endemic countries, especially malaria, schistosomiasis, echinococcosis and African sleeping sickness. However, major limitations of current ‘traditional’ methods for diagnosis are neither simple nor convenient for population surveillance, and showed low sensitivity and specificity. Access to novel technologies for the development of adequate and reliable tools are expressly needed. A collaborative project between African Network for Drugs and Diagnostics Innovation and partner institutions in Africa and China aims to screen suitable serological biomarkers for diagnostic pipelines against these ‘diseases of the poor’. METHODS: Parasite-specific exposed versus unexposed individuals were screened and sera or urine/stools were collected through case-control studies in China and African countries. Target genes/open reading frames were selected, then will be cloned and cell-free expressed, quantified and immuno-detected. Target antigens/epitopes will be probed and screened with sera from exposed or unexposed individuals using a high-throughput antigen screening platform as the study progresses. The specificity and sensitivity of highly immunoreactive biomarkers will be evaluated as well, using enzyme-linked immunosorbent assays or dipsticks. DISCUSSION: This roadmap explicitly unfolds the integrated operating procedures with focus on malaria and schistosomiasis, for the identification of suitable biomarkers that will aid the prioritization of diagnostics for population use. However, there is need to further validate any new diagnostic through comparison with standard methods in field deployable tests for each region. Our expectations for the future are to seek regulatory approval and promote the use of diagnostics in endemic areas. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40249-017-0344-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-56239702017-10-12 Study roadmap for high-throughput development of easy to use and affordable biomarkers as diagnostics for tropical diseases: a focus on malaria and schistosomiasis Kassegne, Kokouvi Zhang, Ting Chen, Shen-Bo Xu, Bin Dang, Zhi-Sheng Deng, Wang-Ping Abe, Eniola Michael Shen, Hai-Mo Hu, Wei Guyo, Takele Geressu Nwaka, Solomon Chen, Jun-Hu Zhou, Xiao-Nong Infect Dis Poverty Study Protocol BACKGROUND: Interventions are currently being used against ‘infectious diseases of poverty’, which remain highly debilitating and deadly in most endemic countries, especially malaria, schistosomiasis, echinococcosis and African sleeping sickness. However, major limitations of current ‘traditional’ methods for diagnosis are neither simple nor convenient for population surveillance, and showed low sensitivity and specificity. Access to novel technologies for the development of adequate and reliable tools are expressly needed. A collaborative project between African Network for Drugs and Diagnostics Innovation and partner institutions in Africa and China aims to screen suitable serological biomarkers for diagnostic pipelines against these ‘diseases of the poor’. METHODS: Parasite-specific exposed versus unexposed individuals were screened and sera or urine/stools were collected through case-control studies in China and African countries. Target genes/open reading frames were selected, then will be cloned and cell-free expressed, quantified and immuno-detected. Target antigens/epitopes will be probed and screened with sera from exposed or unexposed individuals using a high-throughput antigen screening platform as the study progresses. The specificity and sensitivity of highly immunoreactive biomarkers will be evaluated as well, using enzyme-linked immunosorbent assays or dipsticks. DISCUSSION: This roadmap explicitly unfolds the integrated operating procedures with focus on malaria and schistosomiasis, for the identification of suitable biomarkers that will aid the prioritization of diagnostics for population use. However, there is need to further validate any new diagnostic through comparison with standard methods in field deployable tests for each region. Our expectations for the future are to seek regulatory approval and promote the use of diagnostics in endemic areas. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40249-017-0344-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-02 /pmc/articles/PMC5623970/ /pubmed/28965490 http://dx.doi.org/10.1186/s40249-017-0344-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Kassegne, Kokouvi
Zhang, Ting
Chen, Shen-Bo
Xu, Bin
Dang, Zhi-Sheng
Deng, Wang-Ping
Abe, Eniola Michael
Shen, Hai-Mo
Hu, Wei
Guyo, Takele Geressu
Nwaka, Solomon
Chen, Jun-Hu
Zhou, Xiao-Nong
Study roadmap for high-throughput development of easy to use and affordable biomarkers as diagnostics for tropical diseases: a focus on malaria and schistosomiasis
title Study roadmap for high-throughput development of easy to use and affordable biomarkers as diagnostics for tropical diseases: a focus on malaria and schistosomiasis
title_full Study roadmap for high-throughput development of easy to use and affordable biomarkers as diagnostics for tropical diseases: a focus on malaria and schistosomiasis
title_fullStr Study roadmap for high-throughput development of easy to use and affordable biomarkers as diagnostics for tropical diseases: a focus on malaria and schistosomiasis
title_full_unstemmed Study roadmap for high-throughput development of easy to use and affordable biomarkers as diagnostics for tropical diseases: a focus on malaria and schistosomiasis
title_short Study roadmap for high-throughput development of easy to use and affordable biomarkers as diagnostics for tropical diseases: a focus on malaria and schistosomiasis
title_sort study roadmap for high-throughput development of easy to use and affordable biomarkers as diagnostics for tropical diseases: a focus on malaria and schistosomiasis
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623970/
https://www.ncbi.nlm.nih.gov/pubmed/28965490
http://dx.doi.org/10.1186/s40249-017-0344-9
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