Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Nat Rev Microbiol. 2024 Dec;22(12):756-772. doi: 10.1038/s41579-024-01065-7. Epub 2024 Jul 18.
Malaria killed over 600,000 people in 2022, a death toll that has not improved since 2015. Additionally, parasites and mosquitoes resistant to existing interventions are spreading across Africa and other regions. Vaccines offer hope to reduce the mortality burden: the first licensed malaria vaccines, RTS,S and R21, will be widely deployed in 2024 and should substantially reduce childhood deaths. In this Review, we provide an overview of the malaria problem and the Plasmodium parasite, then describe the RTS,S and R21 vaccines (the first vaccines for any human parasitic disease), summarizing their benefits and limitations. We explore next-generation vaccines designed using new knowledge of malaria pathogenesis and protective immunity, which incorporate antigens and platforms to elicit effective immune responses against different parasite stages in human or mosquito hosts. We describe a decision-making process that prioritizes malaria vaccine candidates for development in a resource-constrained environment. Future vaccines might improve upon the protective efficacy of RTS,S or R21 for children, or address the wider malaria scourge by preventing pregnancy malaria, reducing the burden of Plasmodium vivax or accelerating malaria elimination.
2022 年,疟疾导致超过 60 万人死亡,自 2015 年以来,这一死亡人数并未减少。此外,对现有干预措施具有抗药性的寄生虫和蚊子正在非洲和其他地区蔓延。疫苗为减轻死亡率带来了希望:第一种获得许可的疟疾疫苗 RTS,S 和 R21 将在 2024 年广泛部署,应该会大大减少儿童死亡人数。在这篇综述中,我们概述了疟疾问题和疟原虫寄生虫,然后描述了 RTS,S 和 R21 疫苗(第一种针对任何人类寄生虫病的疫苗),总结了它们的益处和局限性。我们探讨了使用疟疾发病机制和保护性免疫的新知识设计的下一代疫苗,这些疫苗结合了抗原和平台,以在人类或蚊子宿主中针对不同寄生虫阶段引发有效的免疫反应。我们描述了一个决策过程,该过程优先考虑在资源有限的环境中开发疟疾疫苗候选物。未来的疫苗可能会提高 RTS,S 或 R21 对儿童的保护效力,或者通过预防妊娠疟疾、减轻间日疟原虫的负担或加速疟疾消除来解决更广泛的疟疾问题。