Abstract

Background Plasmodium knowlesi (Pk), a simian malaria parasite, is a suitable primate model for Plasmodium falciparum (Pf), and it was recently identified as the fifth human malaria parasite [1]. To test the ability of yeast-expressed PkAMA1 (Figure 1) to protect rhesus macaques upon challenge with Pk, six healthy rhesus monkeys were vaccinated with PkAMA1 and six control monkeys were vaccinated with PfAMA1 formulated in an oil in water adjuvant [2]. All monkeys received three i.m. vaccinations at 4 week intervals. Results PkAMA1 monkeys produced antibodies that inhibited Pk growth in vitro. Monkeys were challenged two weeks after the third vaccination with Pk blood stage parasites and parasitaemia was followed for 3 weeks. Five out of six controls and one PkAMA1 animal developed fulminent parasitaemias. Four out of six PkAMA1 vaccinated monkeys delayed the onset of the parasitaemia (> 2 days) and one animal in the PkAMA1 group was able to completely control parasitaemia, which correlated with the level of parasite growth inhibitory antibodies. PkAMA1

Highlights

  • Plasmodium knowlesi (Pk), a simian malaria parasite, is a suitable primate model for Plasmodium falciparum (Pf), and it was recently identified as the fifth human malaria parasite [1]

  • Monkeys were challenged two weeks after the third vaccination with Pk blood stage parasites and parasitaemia was followed for 3 weeks

  • Four out of six PkAMA1 vaccinated monkeys delayed the onset of the parasitaemia (> 2 days) and one animal in the PkAMA1 group was able to completely control parasitaemia, which correlated with the level of parasite growth inhibitory antibodies

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Summary

Open Access

Muzamil Mahdi Abdel Hamid1*, Edmond J Remarque[2], Bart W Faber[2], Leonie M van Duivenvoorde[2], Clemens HM Kocken[2], Alan W Thomas[2]. From Parasite to Prevention: Advances in the understanding of malaria Edinburgh, UK. From Parasite to Prevention: Advances in the understanding of malaria Edinburgh, UK. 20-22 October 2010

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