Plasmodium falciparum Clearance Is Pitting-Dependent With Artemisinin-Based Drugs but Pitting-Independent With Atovaquone-Proguanil or Mefloquine

J Infect Dis. 2019 Jul 2;220(3):535-539. doi: 10.1093/infdis/jiz115.

Abstract

Pitting, the removal of dead parasites from their host erythrocyte, has been studied in patients with severe malaria treated parenterally with quinine or artesunate, and was recently shown to contribute to delayed hemolysis, a frequent adverse event of artesunate. We quantified pitting in 81 travelers treated with oral antimalarial therapy. Pitting rate was high (55.8%) with artemisinin-based combinations, but <10% with the nonartemisinin drugs quinine, mefloquine, and atovaquone-proguanil. This may, in part, explain the slower parasite clearance in patients treated with antimalarial drugs lacking an artemisinin component, as well as the absence of posttreatment hemolysis with these drugs.

Keywords: artemisinin derivatives combination therapy; atovaquone-proguanil; malaria parasite clearance; pitting; postartemisinin delayed hemolysis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Antimalarials / pharmacology*
  • Artemisinins / pharmacology*
  • Artesunate / pharmacology
  • Atovaquone / pharmacology*
  • Child
  • Drug Combinations
  • Female
  • Humans
  • Malaria, Falciparum / drug therapy*
  • Malaria, Falciparum / parasitology
  • Male
  • Mefloquine / pharmacology*
  • Middle Aged
  • Plasmodium falciparum / drug effects*
  • Proguanil / pharmacology*
  • Young Adult

Substances

  • Antimalarials
  • Artemisinins
  • Drug Combinations
  • atovaquone, proguanil drug combination
  • Artesunate
  • artemisinin
  • Proguanil
  • Mefloquine
  • Atovaquone