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Artemisinin-Based Antimalarial Drug Therapy: Molecular Pharmacology and Evolving Resistance
The molecular pharmacology of artemisinin (ART)-based antimalarial drugs is incompletely understood. Clinically, these drugs are used in combination with longer lasting partner drugs in several different artemisinin combination therapies (ACTs). ACTs are currently the standard of care against Plasmo...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631165/ https://www.ncbi.nlm.nih.gov/pubmed/31167396 http://dx.doi.org/10.3390/tropicalmed4020089 |
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author | Heller, Laura E. Roepe, Paul D. |
author_facet | Heller, Laura E. Roepe, Paul D. |
author_sort | Heller, Laura E. |
collection | PubMed |
description | The molecular pharmacology of artemisinin (ART)-based antimalarial drugs is incompletely understood. Clinically, these drugs are used in combination with longer lasting partner drugs in several different artemisinin combination therapies (ACTs). ACTs are currently the standard of care against Plasmodium falciparum malaria across much of the world. A harbinger of emerging artemisinin resistance (ARTR), known as the delayed clearance phenotype (DCP), has been well documented in South East Asia (SEA) and is beginning to affect the efficacy of some ACTs. Though several genetic mutations have been associated with ARTR/DCP, a molecular mechanism remains elusive. This paper summarizes our current understanding of ART molecular pharmacology and hypotheses for ARTR/DCP. |
format | Online Article Text |
id | pubmed-6631165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66311652019-08-19 Artemisinin-Based Antimalarial Drug Therapy: Molecular Pharmacology and Evolving Resistance Heller, Laura E. Roepe, Paul D. Trop Med Infect Dis Review The molecular pharmacology of artemisinin (ART)-based antimalarial drugs is incompletely understood. Clinically, these drugs are used in combination with longer lasting partner drugs in several different artemisinin combination therapies (ACTs). ACTs are currently the standard of care against Plasmodium falciparum malaria across much of the world. A harbinger of emerging artemisinin resistance (ARTR), known as the delayed clearance phenotype (DCP), has been well documented in South East Asia (SEA) and is beginning to affect the efficacy of some ACTs. Though several genetic mutations have been associated with ARTR/DCP, a molecular mechanism remains elusive. This paper summarizes our current understanding of ART molecular pharmacology and hypotheses for ARTR/DCP. MDPI 2019-06-04 /pmc/articles/PMC6631165/ /pubmed/31167396 http://dx.doi.org/10.3390/tropicalmed4020089 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Heller, Laura E. Roepe, Paul D. Artemisinin-Based Antimalarial Drug Therapy: Molecular Pharmacology and Evolving Resistance |
title | Artemisinin-Based Antimalarial Drug Therapy: Molecular Pharmacology and Evolving Resistance |
title_full | Artemisinin-Based Antimalarial Drug Therapy: Molecular Pharmacology and Evolving Resistance |
title_fullStr | Artemisinin-Based Antimalarial Drug Therapy: Molecular Pharmacology and Evolving Resistance |
title_full_unstemmed | Artemisinin-Based Antimalarial Drug Therapy: Molecular Pharmacology and Evolving Resistance |
title_short | Artemisinin-Based Antimalarial Drug Therapy: Molecular Pharmacology and Evolving Resistance |
title_sort | artemisinin-based antimalarial drug therapy: molecular pharmacology and evolving resistance |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631165/ https://www.ncbi.nlm.nih.gov/pubmed/31167396 http://dx.doi.org/10.3390/tropicalmed4020089 |
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