The Benefits of Artemisinin Combination Therapy for Malaria Extend Beyond the Individual Patient

0287 T he traditional, low-cost mainstay drugs for malaria, chloroquine (CQ) and sulphadoxine-pyrimethamine (SP), have a very limited lifetime left in terms of their clinical usefulness. These drugs have been relatively ineffective in Asia for two decades, and rising drug resistance levels have now also rendered them ineffective in many sub-Saharan African countries [1]. Artemisinin drugs, such as artesunate and artemether, derived from the Chinese herb Artemisia annua, are rapidly being adopted as standard treatments in Africa, in the hope that effective treatment will assist in reversing the apparently increasing death rates in African children [2]. In the most severe form of human malaria, Plasmodium falciparum, adequate treatment of a malaria attack does not necessarily prevent the infected person from transmitting the disease to others. Mosquitoes become infected by ingesting mature sexual stages, known as gametocytes, which take around ten days to develop. Mature gametocytes present at the time of treatment may be unaffected, and parasites already committed to gametogenesis at the time of treatment will continue their development. Therefore, infectious gametocytes may be present in the blood for many days after the patient has been treated and feels better. Gametocytes responsible for such " post-treatment transmission " are more likely to carry and spread drug-resistant alleles [3]. Trials showed that adding three days of the artemisinin derivative artesunate to existing antimalarial treatments led to a marked reduction in the number of gametocytes in the month following the treatment [4]. Whether this translates to an impact on transmission is less clear: in an area of low transmission in western Thailand, the introduction of artesunate in 1994 coincided with a sustained decrease in incidence of malaria [5]. However, infectiousness of patients to mosquitoes in this study was not measured directly, and the association of drug introduction and incidence reduction may have been coincidental. A randomized controlled study by Sutherland and colleagues in this month's PLoS Medicine [6] shows conclusively that a six-dose course of artemether-lumefantrine (co-artemether) given to children with P. falciparum malaria in Gambia reduces gametocyte prevalence, duration of gametocyte carriage, and infectiousness to mosquitoes, compared to dual treatment with CQ and SP (CQ/SP). Presumably owing to lower gametocyte density, none of the artemether-lumefantrine-treated gametocyte carriers were infectious on day 7 after treatment, compared to 37% of the CQ/SP-treated children. The results also show that artemether-lumefantrine has a specifi c action against developing gametocytes in addition to its action on …