Abstract

BackgroundThe time necessary for malaria parasite to re-appear in the blood following treatment (re-infection time) is an indirect method for evaluating the immune defences operating against pre-erythrocytic and early erythrocytic malaria stages. Few longitudinal data are available in populations in whom malaria transmission level had also been measured.MethodsOne hundred and ten individuals from the village of Ndiop (Senegal), aged between one and 72 years, were cured of malaria by quinine (25 mg/day oral Quinimax™ in three equal daily doses, for seven days). Thereafter, thick blood films were examined to detect the reappearance of Plasmodium falciparum every week, for 11 weeks after treatment. Malaria transmission was simultaneously measured weekly by night collection of biting mosquitoes.ResultsMalaria transmission was on average 15.3 infective bites per person during the 77 days follow up. The median reappearance time for the whole study population was 46.8 days, whereas individuals would have received an average one infective bite every 5 days. At the end of the follow-up, after 77 days, 103 of the 110 individuals (93.6%; CI 95% [89.0–98.2]) had been re-infected with P. falciparum. The median reappearance time ('re-positivation') was longer in subjects with patent parasitaemia at enrolment than in parasitologically-negative individuals (58 days vs. 45.9; p = 0.03) and in adults > 30 years than in younger subjects (58.6 days vs. 42.7; p = 0.0002). In a multivariate Cox PH model controlling for the sickle cell trait, G6PD deficiency and the type of habitat, the presence of parasitaemia at enrolment and age ≥ 30 years were independently predictive of a reduced risk of re-infection (PH = 0.5 [95% CI: 0.3–0.9] and 0.4; [95% CI: 0.2–0.6] respectively).ConclusionResults indicate the existence of a substantial resistance to sporozoites inoculations, but which was ultimately overcome in almost every individual after 2 1/2 months of natural challenges. Such a study design and the results obtained suggest that, despite a small sample size, this approach can contribute to assess the impact of intervention methods, such as the efficacy vector-control measures or of malaria pre-erythrocytic stages vaccines.

Highlights

  • The time necessary for malaria parasite to re-appear in the blood following treatment is an indirect method for evaluating the immune defences operating against pre-erythrocytic and early erythrocytic malaria stages

  • The acquisition of a state of protection against clinical malaria, called premunition, by individuals who are regularly infected with Plasmodium falciparum enables them to control parasite densities to low levels and, thereby, to reduce the incidence of clinical malaria episodes

  • Exposure to infected mosquitoe bites induces immune responses to sporozoite surface antigens and their intensity is a function of the Entomological Inoculation Rate (EIR), and, obviously, of age, reflecting the cumulative number of sporozoites received [3,4,5,6]

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Summary

Introduction

The time necessary for malaria parasite to re-appear in the blood following treatment (re-infection time) is an indirect method for evaluating the immune defences operating against pre-erythrocytic and early erythrocytic malaria stages. The acquisition of a state of protection against clinical malaria, called premunition, by individuals who are regularly infected with Plasmodium falciparum enables them to control parasite densities to low levels and, thereby, to reduce the incidence of clinical malaria episodes. This control is usually considered to be mainly induced by and effective against erythrocytic forms of P. falciparum [1]. It has been proposed that the protection acquired by exposure to infection, may extend to other stages including pre-erythrocytic forms [2]. Acquired antibodies strongly inhibit sporozoite invasion into hepatocytes under in vitro conditions [7]

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