4.7 Review

Elucidating Mechanisms of Drug-Resistant Plasmodium falciparum

Journal

CELL HOST & MICROBE
Volume 26, Issue 1, Pages 35-47

Publisher

CELL PRESS
DOI: 10.1016/j.chom.2019.06.001

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Funding

  1. NIH [R38 AI50234, R01AI124678, R01 AI109023, NRSA T32 AI120578]

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Intensified treatment and control efforts since the early 2000s have dramatically reduced the burden of Plasmodium falciparum malaria. However, drug resistance threatens to derail this progress. In this review, we present four antimalarial resistance case studies that differ in timeline, technical approaches, mechanisms of action, and categories of resistance: chloroquine, sulfadoxine-pyrimethamine, artemisinin, and piperaquine. Lessons learned from prior losses of treatment efficacy, drug combinations, and control strategies will help advance mechanistic research into how P. falciparum parasites acquire resistance to current first-line artemisinin-based combination therapies. Understanding resistance in the clinic and laboratory is essential to prolong the effectiveness of current antimalarial drugs and to optimize the pipeline of future medicines.

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