Molecular assays for antimalarial drug resistance surveillance: A target product profile
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. Antimalarial drug resistance is...
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th-mahidol.446902019-08-23T17:29:00Z Molecular assays for antimalarial drug resistance surveillance: A target product profile Christian Nsanzabana Frederic Ariey Hans Peter Beck Xavier C. Ding Edwin Kamau Sanjeev Krishna Eric Legrand Naomi Lucchi Olivo Miotto Sidsel Nag Harald Noedl Cally Roper Philip J. Rosenthal Henk D.F.H. Schallig Steve M. Taylor Sarah K. Volkman Iveth J. Gonzalez Duke University Medical Center Medizinische Universitat Wien, Zentrum für Pathophysiologie, Infektiologie und Immunologie Foundation for Innovative New Diagnostics, Switzerland Harvard School of Public Health London School of Hygiene & Tropical Medicine Københavns Universitet St George's University of London Universite Paris Descartes University of Oxford University of California, San Francisco Universitat Basel Swiss Tropical and Public Health Institute (Swiss TPH) Centers for Disease Control and Prevention Hopital Cochin AP-HP Copenhagen University Hospital Walter Reed Army Institute of Research Mahidol University United States Army Wellcome Sanger Institute University of Amsterdam Institut Pasteur, Paris Broad Institute Simmons University Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. Antimalarial drug resistance is a major constraint for malaria control and elimination efforts. Artemisinin-based combination therapy is now the mainstay for malaria treatment. However, delayed parasite clearance following treatment with artemisinin derivatives has now spread in the Greater Mekong Sub region and may emerge or spread to other malaria endemic regions. This spread is of great concern for malaria control programmes, as no alternatives to artemisinin-based combination therapies are expected to be available in the near future. There is a need to strengthen surveillance systems for early detection and response to the antimalarial drug resistance threat. Current surveillance is mainly done through therapeutic efficacy studies; however these studies are complex and both time- and resource-intensive. For multiple common antimalarials, parasite drug resistance has been correlated with specific genetic mutations, and the molecular markers associated with antimalarial drug resistance offer a simple and powerful tool to monitor the emergence and spread of resistant parasites. Different techniques to analyse molecular markers associated with antimalarial drug resistance are available, each with advantages and disadvantages. However, procedures are not adequately harmonized to facilitate comparisons between sites. Here we describe the target product profiles for tests to analyse molecular markers associated with antimalarial drug resistance, discuss how use of current techniques can be standardised, and identify the requirements for an ideal product that would allow malaria endemic countries to provide useful spatial and temporal information on the spread of resistance. 2019-08-23T10:14:54Z 2019-08-23T10:14:54Z 2018-09-01 Article PLoS ONE. Vol.13, No.9 (2018) 10.1371/journal.pone.0204347 19326203 2-s2.0-85053676487 https://repository.li.mahidol.ac.th/handle/123456789/44690 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053676487&origin=inward |
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Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology Christian Nsanzabana Frederic Ariey Hans Peter Beck Xavier C. Ding Edwin Kamau Sanjeev Krishna Eric Legrand Naomi Lucchi Olivo Miotto Sidsel Nag Harald Noedl Cally Roper Philip J. Rosenthal Henk D.F.H. Schallig Steve M. Taylor Sarah K. Volkman Iveth J. Gonzalez Molecular assays for antimalarial drug resistance surveillance: A target product profile |
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This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. Antimalarial drug resistance is a major constraint for malaria control and elimination efforts. Artemisinin-based combination therapy is now the mainstay for malaria treatment. However, delayed parasite clearance following treatment with artemisinin derivatives has now spread in the Greater Mekong Sub region and may emerge or spread to other malaria endemic regions. This spread is of great concern for malaria control programmes, as no alternatives to artemisinin-based combination therapies are expected to be available in the near future. There is a need to strengthen surveillance systems for early detection and response to the antimalarial drug resistance threat. Current surveillance is mainly done through therapeutic efficacy studies; however these studies are complex and both time- and resource-intensive. For multiple common antimalarials, parasite drug resistance has been correlated with specific genetic mutations, and the molecular markers associated with antimalarial drug resistance offer a simple and powerful tool to monitor the emergence and spread of resistant parasites. Different techniques to analyse molecular markers associated with antimalarial drug resistance are available, each with advantages and disadvantages. However, procedures are not adequately harmonized to facilitate comparisons between sites. Here we describe the target product profiles for tests to analyse molecular markers associated with antimalarial drug resistance, discuss how use of current techniques can be standardised, and identify the requirements for an ideal product that would allow malaria endemic countries to provide useful spatial and temporal information on the spread of resistance. |
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Duke University Medical Center |
author_facet |
Duke University Medical Center Christian Nsanzabana Frederic Ariey Hans Peter Beck Xavier C. Ding Edwin Kamau Sanjeev Krishna Eric Legrand Naomi Lucchi Olivo Miotto Sidsel Nag Harald Noedl Cally Roper Philip J. Rosenthal Henk D.F.H. Schallig Steve M. Taylor Sarah K. Volkman Iveth J. Gonzalez |
format |
Article |
author |
Christian Nsanzabana Frederic Ariey Hans Peter Beck Xavier C. Ding Edwin Kamau Sanjeev Krishna Eric Legrand Naomi Lucchi Olivo Miotto Sidsel Nag Harald Noedl Cally Roper Philip J. Rosenthal Henk D.F.H. Schallig Steve M. Taylor Sarah K. Volkman Iveth J. Gonzalez |
author_sort |
Christian Nsanzabana |
title |
Molecular assays for antimalarial drug resistance surveillance: A target product profile |
title_short |
Molecular assays for antimalarial drug resistance surveillance: A target product profile |
title_full |
Molecular assays for antimalarial drug resistance surveillance: A target product profile |
title_fullStr |
Molecular assays for antimalarial drug resistance surveillance: A target product profile |
title_full_unstemmed |
Molecular assays for antimalarial drug resistance surveillance: A target product profile |
title_sort |
molecular assays for antimalarial drug resistance surveillance: a target product profile |
publishDate |
2019 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/44690 |
_version_ |
1763495909229854720 |