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Updated: Jan 21, 2026

15:03
Building a Better Mosquito: Identifying the Genes Enabling Malaria and Dengue Fever Resistance in A. gambiae and A. aegypti Mosquitoes
Published on: July 4, 2007
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8-Aminoquinoline Therapy for Latent Malaria
1Eijkman-Oxford Clinical Research Unit, Eijkman Institute for Molecular Biology, Jakarta, Indonesia kbaird@eocru.org.
Clinical Microbiology Reviews
|August 2, 2019
Summary
8-aminoquinoline drugs treat malaria but can cause dangerous red blood cell destruction in G6PD-deficient individuals. Research is needed for safer malaria therapies for all patients.
Area of Science:
- Pharmacology
- Tropical Medicine
- Drug Discovery
Background:
- 8-aminoquinolines represent a critical class of antimalarial drugs.
- Their history spans from early synthesis to modern applications, marked by significant scientific and clinical challenges.
- Key drugs include plasmochin, primaquine, and tafenoquine, each with distinct therapeutic roles and limitations.
Purpose of the Study:
- To review the technical evolution and clinical practice of 8-aminoquinoline antimalarial therapy.
- To analyze the historical development and scientific insights derived from these drugs.
- To explore strategies for overcoming the limitations of current 8-aminoquinolines, particularly hemolytic toxicity.
Main Methods:
- Historical review of scientific literature and clinical data.
- Analysis of drug development timelines and regulatory approvals.
- Examination of the biochemical basis of drug toxicity, specifically glucose-6-phosphate dehydrogenase (G6PD) deficiency.
Main Results:
- 8-aminoquinolines have been pivotal in malaria treatment, offering cures for latent infections.
- Hemolytic crises, linked to G6PD deficiency, have been a persistent challenge since the introduction of primaquine.
- Tafenoquine, approved in 2018, offers extended prophylaxis but still carries risks for G6PD-deficient patients.
Conclusions:
- The hemolytic toxicity of 8-aminoquinolines remains a significant barrier to their widespread use.
- Despite challenges, these drugs provide essential treatment options for malaria.
- Future research should prioritize developing novel antimalarials that are safe for G6PD-deficient populations.
Keywords:
8-aminoquinolinesCYP2D6G6PD deficiencyPlasmodium vivaxhemolytic toxicitylatencyplasmochinprimaquinetafenoquinetherapyMore Related Videos
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