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Drug Resistance in Visceral Leishmaniasis

Visceral leishmaniasis remains a public health problem worldwide. This illness was included by the World Health Organization in the list of neglected tropical diseases targeted for elimination by 2015. The widespread emergence of resistance to pentavalent antimonials in India where half cases occur...

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Detalles Bibliográficos
Autor principal: Maltezou, Helena C.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771279/
https://www.ncbi.nlm.nih.gov/pubmed/19888437
http://dx.doi.org/10.1155/2010/617521
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author Maltezou, Helena C.
author_facet Maltezou, Helena C.
author_sort Maltezou, Helena C.
collection PubMed
description Visceral leishmaniasis remains a public health problem worldwide. This illness was included by the World Health Organization in the list of neglected tropical diseases targeted for elimination by 2015. The widespread emergence of resistance to pentavalent antimonials in India where half cases occur globally and the unavailability of a vaccine in clinical use constitute major obstacles in achieving this goal. The last decade new antileishmanials became available, including the oral agent miltefosine. However, in poor endemic countries their wide use was curtailed because of the high costs, and also due to concerns of toxicity and emergence of resistance. Various mechanisms of antileishmanial resistance were identified recently in field isolates. Their elucidation will boost the design of new drugs and the molecular surveillance of resistance. Combination regimens should be evaluated in large trials. Overall, the development of antileishmanials has been generally slow; new drugs are needed. In order to control visceral leishmaniasis worldwide, treatment advances should become affordable in the poorest countries, where they are needed most.
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spelling pubmed-27712792009-11-03 Drug Resistance in Visceral Leishmaniasis Maltezou, Helena C. J Biomed Biotechnol Review Article Visceral leishmaniasis remains a public health problem worldwide. This illness was included by the World Health Organization in the list of neglected tropical diseases targeted for elimination by 2015. The widespread emergence of resistance to pentavalent antimonials in India where half cases occur globally and the unavailability of a vaccine in clinical use constitute major obstacles in achieving this goal. The last decade new antileishmanials became available, including the oral agent miltefosine. However, in poor endemic countries their wide use was curtailed because of the high costs, and also due to concerns of toxicity and emergence of resistance. Various mechanisms of antileishmanial resistance were identified recently in field isolates. Their elucidation will boost the design of new drugs and the molecular surveillance of resistance. Combination regimens should be evaluated in large trials. Overall, the development of antileishmanials has been generally slow; new drugs are needed. In order to control visceral leishmaniasis worldwide, treatment advances should become affordable in the poorest countries, where they are needed most. Hindawi Publishing Corporation 2010 2009-11-01 /pmc/articles/PMC2771279/ /pubmed/19888437 http://dx.doi.org/10.1155/2010/617521 Text en Copyright © 2010 Helena C. Maltezou. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Maltezou, Helena C.
Drug Resistance in Visceral Leishmaniasis
title Drug Resistance in Visceral Leishmaniasis
title_full Drug Resistance in Visceral Leishmaniasis
title_fullStr Drug Resistance in Visceral Leishmaniasis
title_full_unstemmed Drug Resistance in Visceral Leishmaniasis
title_short Drug Resistance in Visceral Leishmaniasis
title_sort drug resistance in visceral leishmaniasis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771279/
https://www.ncbi.nlm.nih.gov/pubmed/19888437
http://dx.doi.org/10.1155/2010/617521
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