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A Step Toward Eradication of Human Filariases in Areas Where Loa Is Endemic

Mass drug administration (MDA) programs have achieved remarkable success in limiting the pathology and transmission of the human parasitic infections onchocerciasis and lymphatic filariasis. The full implementation of MDA campaigns for filariasis elimination has been stymied by the unacceptable inci...

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Detalles Bibliográficos
Autor principal: Geary, Timothy G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959516/
https://www.ncbi.nlm.nih.gov/pubmed/27073095
http://dx.doi.org/10.1128/mBio.00456-16
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author Geary, Timothy G.
author_facet Geary, Timothy G.
author_sort Geary, Timothy G.
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description Mass drug administration (MDA) programs have achieved remarkable success in limiting the pathology and transmission of the human parasitic infections onchocerciasis and lymphatic filariasis. The full implementation of MDA campaigns for filariasis elimination has been stymied by the unacceptable incidence of severe adverse events observed following drug treatment of a subset of individuals who harbor high loads of Loa loa microfilaria. Extending MDA strategies to regions where loiasis is coendemic could be done confidently if a simple, inexpensive, and rapid diagnostic method was available that could accurately identify individuals who have L. loa microfilarial loads above the risk threshold and could thus be excluded from treatment. A recent paper in mBio reports the discovery of an antigen unique to L. loa microfilaria that can be detected in blood and urine and may form the basis for such an assay. Further work will reveal whether this discovery will smooth the path to achieve filariasis eradication.
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spelling pubmed-49595162016-07-25 A Step Toward Eradication of Human Filariases in Areas Where Loa Is Endemic Geary, Timothy G. mBio Commentary Mass drug administration (MDA) programs have achieved remarkable success in limiting the pathology and transmission of the human parasitic infections onchocerciasis and lymphatic filariasis. The full implementation of MDA campaigns for filariasis elimination has been stymied by the unacceptable incidence of severe adverse events observed following drug treatment of a subset of individuals who harbor high loads of Loa loa microfilaria. Extending MDA strategies to regions where loiasis is coendemic could be done confidently if a simple, inexpensive, and rapid diagnostic method was available that could accurately identify individuals who have L. loa microfilarial loads above the risk threshold and could thus be excluded from treatment. A recent paper in mBio reports the discovery of an antigen unique to L. loa microfilaria that can be detected in blood and urine and may form the basis for such an assay. Further work will reveal whether this discovery will smooth the path to achieve filariasis eradication. American Society for Microbiology 2016-04-12 /pmc/articles/PMC4959516/ /pubmed/27073095 http://dx.doi.org/10.1128/mBio.00456-16 Text en Copyright © 2016 Geary. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
Geary, Timothy G.
A Step Toward Eradication of Human Filariases in Areas Where Loa Is Endemic
title A Step Toward Eradication of Human Filariases in Areas Where Loa Is Endemic
title_full A Step Toward Eradication of Human Filariases in Areas Where Loa Is Endemic
title_fullStr A Step Toward Eradication of Human Filariases in Areas Where Loa Is Endemic
title_full_unstemmed A Step Toward Eradication of Human Filariases in Areas Where Loa Is Endemic
title_short A Step Toward Eradication of Human Filariases in Areas Where Loa Is Endemic
title_sort step toward eradication of human filariases in areas where loa is endemic
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959516/
https://www.ncbi.nlm.nih.gov/pubmed/27073095
http://dx.doi.org/10.1128/mBio.00456-16
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