Malaria Journal

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Treatment of asymptomatic carriers with artemether-lumefantrine: an opportunity to reduce the burden of malaria?

Bernhards Ogutu1,2*, Alfred B Tiono3, Michael Makanga4, Zulfiqarali Premji5, Adama D Gbadoé6, David Ubben7, Anne C Marrast8 and Oumar Gaye9

Author Affiliations

1 Walter Reed Project/Centre for Clinical Research-Kenya Medical Research Institute, Nairobi, Kenya

2 Malaria Clinical Trials Alliance - INDEPTH Network, Nairobi, Kenya

3 Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso

4 European and Developing Countries Clinical Trials, Cape Town, South Africa

5 Department of Parasitology and Medical Entomology, Muhimbili University College of Health Sciences, Dar es Salaam, Tanzania

6 Department of Paediatrics, University of Lomé, Lomé, Togo

7 Medicines for Malaria Venture, Geneva, Switzerland

8 Novartis Pharma AG, Basel, Switzerland

9 Faculty of Medicine, University CAD Dakar, Senegal

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Malaria Journal 2010, 9:30 doi:10.1186/1475-2875-9-30

Published: 22 January 2010

Abstract

Background

Increased investment and commitment to malaria prevention and treatment strategies across Africa has produced impressive reductions in the incidence of this disease. Nevertheless, it is clear that further interventions will be necessary to meet the international target of a reversal in the incidence of malaria by 2015. This article discusses the prospective role of an innovative malaria control strategy - the community-based treatment of asymptomatic carriers of Plasmodium falciparum, with artemisinin-based combination therapy (ACT). The potential of this intervention was considered by key scientists in the field at an Advisory Board meeting held in Basel, in April 2009. This article summarizes the discussions that took place among the participants.

Presentation of the hypothesis

Asymptomatic carriers do not seek treatment for their infection and, therefore, constitute a reservoir of parasites and thus a real public-health risk. The systematic identification and treatment of individuals with asymptomatic P. falciparum as part of a surveillance intervention strategy should reduce the parasite reservoir, and if this pool is greatly reduced, it will impact disease transmission.

Testing the hypothesis

This article considers the populations that could benefit from such a strategy and examines the ethical issues associated with the treatment of apparently healthy individuals, who represent a neglected public health risk. The potential for the treatment of asymptomatic carriers to impair the development of protective immunity, resulting in a 'rebound' and age escalation of malaria incidence, is also discussed.

For policymakers to consider the treatment of asymptomatic carriers with ACT as a new tool in their malaria control programmes, it will be important to demonstrate that such a strategy can produce significant benefits, without having a negative impact on the efficacy of ACT and the health of the target population.

Implications of the hypothesis

The treatment of asymptomatic carriers with ACT is an innovative and essential tool for breaking the cycle of infection in some transmission settings. Safe and effective medicines can save the lives of children, but the reprieve is only temporary so long as the mosquitoes can become re-infected from the asymptomatic carriers. With improvements in rapid diagnostic tests that allow easier identification of asymptomatic carriers, the elimination of the pool of parasites is within reach.