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A discovery and development roadmap for new endectocidal transmission-blocking agents in malaria
Reaching the overall goal of eliminating malaria requires halting disease transmission. One approach to blocking transmission is to prevent passage of the parasite to a mosquito, by preventing formation or transmission of gametocytes. An alternative approach, pioneered in the veterinary field, is to...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6287360/ https://www.ncbi.nlm.nih.gov/pubmed/30526594 http://dx.doi.org/10.1186/s12936-018-2598-5 |
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author | Burrows, Jeremy Slater, Hannah Macintyre, Fiona Rees, Sarah Thomas, Anna Okumu, Fredros Hooft van Huijsduijnen, Rob Duparc, Stephan Wells, Timothy N. C. |
author_facet | Burrows, Jeremy Slater, Hannah Macintyre, Fiona Rees, Sarah Thomas, Anna Okumu, Fredros Hooft van Huijsduijnen, Rob Duparc, Stephan Wells, Timothy N. C. |
author_sort | Burrows, Jeremy |
collection | PubMed |
description | Reaching the overall goal of eliminating malaria requires halting disease transmission. One approach to blocking transmission is to prevent passage of the parasite to a mosquito, by preventing formation or transmission of gametocytes. An alternative approach, pioneered in the veterinary field, is to use endectocides, which are molecules that render vertebrate blood meals toxic for the mosquito vector, also killing the parasite. Field studies and modelling suggest that reducing the lifespan of the mosquito may significantly reduce transmission, given the lengthy maturation process of the parasite. To guide the development of new endectocides, or the reformulation of existing molecules, it is important to construct a framework of the required attributes, commonly called the target candidate profile. Here, using a combination of insights from current endectocides, mathematical models of the malaria transmission dynamics, and known impacts of vector control, a target candidate profile (TCP-6) and a regulatory strategy are proposed for a transmission reducing agent. The parameters chosen can be used to assess the potential of a new medicine, independent of whether it has classical endectocide activity, reduces the insect and parasite lifespan or any combination of all three, thereby constituting an ‘endectocidal transmission blocking’ paradigm. |
format | Online Article Text |
id | pubmed-6287360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62873602018-12-14 A discovery and development roadmap for new endectocidal transmission-blocking agents in malaria Burrows, Jeremy Slater, Hannah Macintyre, Fiona Rees, Sarah Thomas, Anna Okumu, Fredros Hooft van Huijsduijnen, Rob Duparc, Stephan Wells, Timothy N. C. Malar J Review Reaching the overall goal of eliminating malaria requires halting disease transmission. One approach to blocking transmission is to prevent passage of the parasite to a mosquito, by preventing formation or transmission of gametocytes. An alternative approach, pioneered in the veterinary field, is to use endectocides, which are molecules that render vertebrate blood meals toxic for the mosquito vector, also killing the parasite. Field studies and modelling suggest that reducing the lifespan of the mosquito may significantly reduce transmission, given the lengthy maturation process of the parasite. To guide the development of new endectocides, or the reformulation of existing molecules, it is important to construct a framework of the required attributes, commonly called the target candidate profile. Here, using a combination of insights from current endectocides, mathematical models of the malaria transmission dynamics, and known impacts of vector control, a target candidate profile (TCP-6) and a regulatory strategy are proposed for a transmission reducing agent. The parameters chosen can be used to assess the potential of a new medicine, independent of whether it has classical endectocide activity, reduces the insect and parasite lifespan or any combination of all three, thereby constituting an ‘endectocidal transmission blocking’ paradigm. BioMed Central 2018-12-10 /pmc/articles/PMC6287360/ /pubmed/30526594 http://dx.doi.org/10.1186/s12936-018-2598-5 Text en © The Author(s) 2018 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 | Review Burrows, Jeremy Slater, Hannah Macintyre, Fiona Rees, Sarah Thomas, Anna Okumu, Fredros Hooft van Huijsduijnen, Rob Duparc, Stephan Wells, Timothy N. C. A discovery and development roadmap for new endectocidal transmission-blocking agents in malaria |
title | A discovery and development roadmap for new endectocidal transmission-blocking agents in malaria |
title_full | A discovery and development roadmap for new endectocidal transmission-blocking agents in malaria |
title_fullStr | A discovery and development roadmap for new endectocidal transmission-blocking agents in malaria |
title_full_unstemmed | A discovery and development roadmap for new endectocidal transmission-blocking agents in malaria |
title_short | A discovery and development roadmap for new endectocidal transmission-blocking agents in malaria |
title_sort | discovery and development roadmap for new endectocidal transmission-blocking agents in malaria |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6287360/ https://www.ncbi.nlm.nih.gov/pubmed/30526594 http://dx.doi.org/10.1186/s12936-018-2598-5 |
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