Affiliation:
1. Australian Army Malaria Institute, Enoggera, Brisbane, QLD, Australia
2. Novartis Institute of Tropical Diseases, Singapore
Abstract
ABSTRACT
In vitro
drug treatment with artemisinin derivatives, such as dihydroartemisinin (DHA), results in a temporary growth arrest (i.e., dormancy) at an early ring stage in
Plasmodium falciparum
. This response has been proposed to play a role in the recrudescence of
P. falciparum
infections following monotherapy with artesunate and may contribute to the development of artemisinin resistance in
P. falciparum
malaria. We demonstrate here that artemether does induce dormant rings, a finding which further supports the class effect of artemisinin derivatives in inducing the temporary growth arrest of
P. falciparum
parasites. In contrast and similarly to lumefantrine, the novel and fast-acting spiroindolone compound KAE609 does not induce growth arrest at the early ring stage of
P. falciparum
and prevents the recrudescence of DHA-arrested rings at a low concentration (50 nM). Our findings, together with previous clinical data showing that KAE609 is active against artemisinin-resistant K13 mutant parasites, suggest that KAE609 could be an effective partner drug with a broad range of antimalarials, including artemisinin derivatives, in the treatment of multidrug-resistant
P. falciparum
malaria.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
12 articles.
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