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The emergence of artemisinin partial resistance in Africa: how do we respond?
Rosenthal, Philip J; Asua, Victor; Bailey, Jeffrey A; Conrad, Melissa D; Ishengoma, Deus S; Kamya, Moses R; Rasmussen, Charlotte; Tadesse, Fitsum G; Uwimana, Aline; Fidock, David A.
Affiliation
  • Rosenthal PJ; Department of Medicine, University of California, San Francisco, CA, USA. Electronic address: philip.rosenthal@ucsf.edu.
  • Asua V; Infectious Diseases Research Collaboration, Kampala, Uganda; University of Tübingen, Tübingen, Germany.
  • Bailey JA; Center for Computational Molecular Biology, Brown University, Providence, RI, USA; Departments of Pathology and Laboratory Medicine, Warren Alpert Medical School, Brown University, Providence, RI, USA.
  • Conrad MD; Department of Medicine, University of California, San Francisco, CA, USA.
  • Ishengoma DS; National Institute for Medical Research, Dar es Salaam, Tanzania; Department of Biochemistry, Kampala International University in Tanzania, Dar es Salaam, Tanzania; School of Public Health, Harvard University, Boston, MA, USA.
  • Kamya MR; Infectious Diseases Research Collaboration, Kampala, Uganda; Department of Medicine, Makerere University, Kampala, Uganda.
  • Rasmussen C; WHO, Geneva, Switzerland.
  • Tadesse FG; Armauer Hansen Research Institute, Addis Ababa, Ethiopia; London School of Hygiene and Tropical Medicine, London, UK.
  • Uwimana A; Rwanda Biomedical Center, Kigali, Rwanda; Louvain Drug Research Institute, Université Catholique de Louvain, Brussels, Belgium.
  • Fidock DA; Department of Microbiology and Immunology and Center for Malaria Therapeutics and Antimicrobial Resistance, Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Lancet Infect Dis ; 2024 Mar 26.
Article de En | MEDLINE | ID: mdl-38552654
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.

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Lancet Infect Dis Sujet du journal: DOENCAS TRANSMISSIVEIS Année: 2024 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Lancet Infect Dis Sujet du journal: DOENCAS TRANSMISSIVEIS Année: 2024 Type de document: Article