4.7 Article

The Novel bis-1,2,4-Triazine MIPS-0004373 Demonstrates Rapid and Potent Activity against All Blood Stages of the Malaria Parasite

期刊

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.00311-21

关键词

malaria; antimalarial; triazine; Plasmodium

资金

  1. Australian National Health and Medical Research Council (NHMRC) [APP1102147, APP1148700, APP1117602]
  2. Medicines for Malaria Venture (MMV)
  3. Ruth L. Kirschstein Institutional National Research Award from the National Institute for General Medical Sciences [T32 GM008666]
  4. MMV grant [RD-08-2800]
  5. Wellcome [100993/Z/13/Z]

向作者/读者索取更多资源

Novel bis-1,2,4-triazine compound MIPS-0004373 demonstrates potent in vitro activity against Plasmodium falciparum parasites, with good efficacy against blood and sexually committed ring stage parasites. The compound also shows activity against liver stage parasites in an in vitro P. berghei model, but limited activity against mature gametocytes. In vivo, MIPS-0004373 efficiently clears established P. berghei infection, with efficacy similar to artesunate and chloroquine.
Novel bis-1,2,4-triazine compounds with potent in vitro activity against Plasmodium falciparum parasites were recently identified. The bis-1,2,4-triazines represent a unique antimalarial pharmacophore and are proposed to act by a novel but as-yet-unknown mechanism of action. This study investigated the activity of the bis-1,2,4-triazine MIPS-0004373 across the mammalian life cycle stages of the parasite and profiled the kinetics of activity against blood and transmission stage parasites in vitro and in vivo. MIPS-0004373 demonstrated rapid and potent activity against P. falciparum, with excellent in vitro activity against all asexual blood stages. Prolonged in vitro drug exposure failed to generate stable resistance de novo, suggesting a low propensity for the emergence of resistance. Excellent activity was observed against sexually committed ring stage parasites, but activity against mature gametocytes was limited to inhibiting male gametogenesis. Assessment of liver stage activity demonstrated good activity in an in vitro P. berghei model but no activity against Plasmodium cynomolgi hypnozoites or liver schizonts. The bis-1,2,4-triazine MIPS-0004373 efficiently cleared an established P. berghei infection in vivo, with efficacy similar to that of artesunate and chloroquine and a recrudescence profile comparable to that of chloroquine. This study demonstrates the suitability of bis-1,2,4-triazines for further development toward a novel treatment for acute malaria.

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