What is it about?

Although there has been major recent progress in malaria vaccine development, substantial challenges remain for achieving highly efficacious and durable vaccines against Plasmodium falciparum and Plasmodium vivax malaria. Greater knowledge of mechanisms and key targets of immunity are needed to accomplish this goal, together with new strategies for generating potent, long-lasting, functional immunity against multiple antigens. Implementation considerations in endemic areas will ultimately affect vaccine effectiveness, so innovations to simplify and enhance delivery are also needed. Whereas challenges remain, recent exciting progress and emerging knowledge promise hope for the future of malaria vaccines.

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Why is it important?

Malaria remains as one of the world’s leading health issues, responsible for >200 million clinical cases and up to 500,000 deaths annually, and is a leading cause of death among young children. The strong need for malaria vaccines with high efficacy to achieve control and elimination is recognized by key global organizations and heightened by the spread of antimalarial drug and insecticide resistance, recent rebound increases in malaria in many regions, and stalled progress toward reducing the global malaria burden

Perspectives

substantial challenges remain to advance beyond the generally modest efficacy demonstrated by existing vaccines tested in malaria-endemic areas and achieve the goal of a highly efficacious and durable vaccine, preferably for both P. falciparum and P. vivax. A deeper understanding of mechanisms and key targets of immunity is needed to underpin this, and research to reveal new strategies for the induction of a higher level of protective functional immunity. Achieving higher efficacy may require vaccines to induce multiple functional mechanisms and may require the inclusion of multiple antigens (of the same stage or across multiple stages), whole attenuated parasites, or innovative vaccine design to induce responses that better target specific protective epitopes compared to established strategies. A lack of correlates of protection to evaluate current vaccines and inform the development of new candidates is a constraint that hinders more expedient progress. Furthermore, most vaccines to date have induced protective immune responses of only short or modest duration, and new insights into how long-lasting immunity can be generated are urgently needed. Ideally, future vaccines will be low cost and affordable and administered in practical formulations and regimens suitable for mass vaccine campaigns and inclusion in childhood EPI. Although challenges remain, recent exciting progress and emerging knowledge promise great hope for the future

James Beeson
Burnet Institute

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This page is a summary of: Challenges and strategies for developing efficacious and long-lasting malaria vaccines, Science Translational Medicine, January 2019, American Association for the Advancement of Science,
DOI: 10.1126/scitranslmed.aau1458.
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