The emergence of artemisinin partial resistance in Africa: how do we respond?
- PMID: 38552654
- DOI: 10.1016/S1473-3099(24)00141-5
The emergence of artemisinin partial resistance in Africa: how do we respond?
Abstract
Malaria remains one of the most important infectious diseases in the world, with the greatest burden in sub-Saharan Africa, primarily from Plasmodium falciparum infection. The treatment and control of malaria is challenged by resistance to most available drugs, but partial resistance to artemisinins (ART-R), the most important class for the treatment of malaria, was until recently confined to southeast Asia. This situation has changed, with the emergence of ART-R in multiple countries in eastern Africa. ART-R is mediated primarily by single point mutations in the P falciparum kelch13 protein, with several mutations present in African parasites that are now validated resistance mediators based on clinical and laboratory criteria. Major priorities at present are the expansion of genomic surveillance for ART-R mutations across the continent, more frequent testing of the efficacies of artemisinin-based regimens against uncomplicated and severe malaria in trials, more regular assessment of ex-vivo antimalarial drug susceptibilities, consideration of changes in treatment policy to deter the spread of ART-R, and accelerated development of new antimalarial regimens to overcome the impacts of ART-R. The emergence of ART-R in Africa is an urgent concern, and it is essential that we increase efforts to characterise its spread and mitigate its impact.
Copyright © 2024 World Health Organization. Published by Elsevier Ltd.. All rights reserved.
Conflict of interest statement
Declaration of interests We declare no competing interests.
Similar articles
-
Emergence, transmission dynamics and mechanisms of artemisinin partial resistance in malaria parasites in Africa.Nat Rev Microbiol. 2024 Jun;22(6):373-384. doi: 10.1038/s41579-024-01008-2. Epub 2024 Feb 6. Nat Rev Microbiol. 2024. PMID: 38321292 Review.
-
Local emergence in Amazonia of Plasmodium falciparum k13 C580Y mutants associated with in vitro artemisinin resistance.Elife. 2020 May 12;9:e51015. doi: 10.7554/eLife.51015. Elife. 2020. PMID: 32394893 Free PMC article.
-
Spatial and molecular mapping of Pfkelch13 gene polymorphism in Africa in the era of emerging Plasmodium falciparum resistance to artemisinin: a systematic review.Lancet Infect Dis. 2021 Apr;21(4):e82-e92. doi: 10.1016/S1473-3099(20)30493-X. Epub 2020 Oct 27. Lancet Infect Dis. 2021. PMID: 33125913
-
Artemisinin Action and Resistance in Plasmodium falciparum.Trends Parasitol. 2016 Sep;32(9):682-696. doi: 10.1016/j.pt.2016.05.010. Epub 2016 Jun 9. Trends Parasitol. 2016. PMID: 27289273 Free PMC article. Review.
-
Emerging threat of artemisinin partial resistance markers (pfk13 mutations) in Plasmodium falciparum parasite populations in multiple geographical locations in high transmission regions of Uganda.Malar J. 2024 Nov 5;23(1):330. doi: 10.1186/s12936-024-05158-9. Malar J. 2024. PMID: 39501325 Free PMC article.
Cited by
-
Slowing the spread of treatment failure to artemisinin-based combination therapies in Uganda.medRxiv [Preprint]. 2025 May 18:2025.05.15.25327701. doi: 10.1101/2025.05.15.25327701. medRxiv. 2025. PMID: 40463542 Free PMC article. Preprint.
-
Genetic surveillance of Plasmodium falciparum populations following treatment policy revisions in the Greater Mekong Subregion.Nat Commun. 2025 May 20;16(1):4689. doi: 10.1038/s41467-025-59946-1. Nat Commun. 2025. PMID: 40394107 Free PMC article.
-
Ex Vivo Drug Susceptibility of Plasmodium malariae Isolates to Antimalarial Drugs in Gabon.Pathogens. 2025 May 6;14(5):453. doi: 10.3390/pathogens14050453. Pathogens. 2025. PMID: 40430773 Free PMC article.
-
Regional action needed to halt antimalarial drug resistance in Africa.Lancet. 2025 Jan 4;405(10472):7-10. doi: 10.1016/S0140-6736(24)02706-5. Epub 2024 Dec 12. Lancet. 2025. PMID: 39674185 Free PMC article. No abstract available.
-
Synthesis of 1,2,3-Triazole-Methyl-Menadione Derivatives: Evaluation of Electrochemical and Antiparasitic Properties against two Blood-Dwelling Parasites.ChemMedChem. 2025 Mar 15;20(6):e202400731. doi: 10.1002/cmdc.202400731. Epub 2025 Jan 8. ChemMedChem. 2025. PMID: 39676716 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources