Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Nat Immunol. 2024 Sep;25(9):1530-1545. doi: 10.1038/s41590-024-01938-2. Epub 2024 Aug 28.
Despite various public health strategies, malaria caused by Plasmodium falciparum parasites remains a major global health challenge that requires development of new interventions. Extended half-life human monoclonal antibodies targeting the P. falciparum circumsporozoite protein on sporozoites, the infective form of malaria parasites, prevent malaria in rodents and humans and have been advanced into clinical development. The protective epitopes on the circumsporozoite protein targeted by monoclonal antibodies have been defined. Cryogenic electron and multiphoton microscopy have enabled mechanistic structural and functional investigations of how antibodies bind to the circumsporozoite protein and neutralize sporozoites. Moreover, innovations in bioinformatics and antibody engineering have facilitated enhancement of antibody potency and durability. Here, we summarize the latest scientific advances in understanding how monoclonal antibodies to the circumsporozoite protein prevent malaria and highlight existing clinical data and future plans for how this emerging intervention can be used alone or alongside existing antimalarial interventions to control malaria across at-risk populations.
尽管采取了各种公共卫生策略,但恶性疟原虫寄生虫引起的疟疾仍然是一个重大的全球健康挑战,需要开发新的干预措施。针对疟原虫孢子虫表面蛋白的延长半衰期人源单克隆抗体可预防啮齿动物和人类疟疾,并已进入临床开发阶段。单克隆抗体针对的孢子虫表面蛋白的保护性表位已被确定。低温电子显微镜和多光子显微镜使我们能够对抗体与孢子虫表面蛋白结合并中和孢子虫的机制结构和功能进行研究。此外,生物信息学和抗体工程方面的创新促进了抗体效力和持久性的提高。在这里,我们总结了对孢子虫表面蛋白单克隆抗体预防疟疾的最新科学进展,并强调了现有临床数据和未来计划,说明这种新出现的干预措施如何单独或与现有的抗疟干预措施一起用于控制高危人群的疟疾。