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Emergence of Plasmodium falciparum triple mutant in Cambodia
The rationale for this combination relies on evidence that parasites carrying markers of resistance both to artemisinin (pfKelch13-580Y mutant) and piperaquine (later associated with the amplification of pfplasmepsin2)3,4 have regained susceptibility to mefloquine (low in vitro IC50 [half maximal in...
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Published in: | The Lancet infectious diseases 2017-12, Vol.17 (12), p.1233-1233 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The rationale for this combination relies on evidence that parasites carrying markers of resistance both to artemisinin (pfKelch13-580Y mutant) and piperaquine (later associated with the amplification of pfplasmepsin2)3,4 have regained susceptibility to mefloquine (low in vitro IC50 [half maximal inhibitory concentration] values and the single-copy pfmdr1, the amplification of which has been associated with mefloquine resistance).2 One valuable hypothesis is that these genetic events could represent counteracting resistance mechanisms, allowing strategies of alternating mefloquine and piperaquine (or a combination of all three drugs) to be considered as reasonable treatment options.In October, 2015, MSF strengthened the malaria passive case detection activity by adding the systematic collection of blood samples for subsequent real-time PCR analysis.5 Over this period, the first-line treatment changed from DHA-PPQ (before February, 2016) to ASMQ (after February, 2016), and 194 clinical cases of P falciparum were confirmed (130 before and 64 after February, 2016).In view of these data, vigilant drug resistance surveillance and investment in alternative treatment options are warranted. |
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ISSN: | 1473-3099 1474-4457 |
DOI: | 10.1016/S1473-3099(17)30635-7 |