Abstract

A vaccine against malaria is urgently needed for control and eventual eradication. Different approaches are pursued to induce either sterile immunity directed against pre-erythrocytic parasites or to mimic naturally acquired immunity by controlling blood-stage parasite densities and disease severity. Pre-erythrocytic and blood-stage malaria vaccines are often seen as opposing tactics, but it is likely that they have to be combined into a multi-stage malaria vaccine to be optimally safe and effective.Since many antigenic targets are shared between liver- and blood-stage parasites, malaria vaccines have the potential to elicit cross-stage protection with immune mechanisms against both stages complementing and enhancing each other. Here we discuss evidence from pre-erythrocytic and blood-stage subunit and whole parasite vaccination approaches that show that protection against malaria is not necessarily stage-specific. Parasites arresting at late liver-stages especially, can induce powerful blood-stage immunity, and similarly exposure to blood-stage parasites can afford pre-erythrocytic immunity.The incorporation of a blood-stage component into a multi-stage malaria vaccine would hence not only combat breakthrough infections in the blood should the pre-erythrocytic component fail to induce sterile protection, but would also actively enhance the pre-erythrocytic potency of this vaccine. We therefore advocate that future studies should concentrate on the identification of cross-stage protective malaria antigens, which can empower multi-stage malaria vaccine development.

Highlights

  • Malaria remains a major global health scourge and there is a general consensus that elimination and eradication efforts will not be successful without an effective malaria vaccine

  • After vaccination of humans with apical membrane antigen 1 (AMA-1) and merozoite surface protein 1 (MSP-1), time to diagnosis, which was delayed in the vaccinees, significantly correlated with liver-to-blood parasite levels but not blood-stage multiplication rates

  • As Plasmodium matures in the liver, it is potentially capable of inducing immunity against preerythrocytic and against blood-stage parasites [36]

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Summary

Background

Malaria remains a major global health scourge and there is a general consensus that elimination and eradication efforts will not be successful without an effective malaria vaccine. Immunity against severe disease caused by bloodstage parasites can be acquired after only one or two infections, while infections with high parasite densities still occur [1]. Vaccines targeting blood-stage parasites should induce control of (severe) disease but clearance of blood-stage parasites. This is essential as gametocytes form during blood-stage infection and transmission to mosquitoes can otherwise continue

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