Jelínková Lucie, Flores-Garcia Yevel, Shapiro Sarah, Roberts Bryce T, Petrovsky Nikolai, Zavala Fidel, Chackerian Bryce
Department of Molecular Genetics and Microbiology, University of New Mexico School of Medicine, Albuquerque, NM, USA.
W. Harry Feinstone Department of Molecular Microbiology and Immunology Malaria Research Institute, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
NPJ Vaccines. 2022 Mar 8;7(1):34. doi: 10.1038/s41541-022-00457-1.
Pre-erythrocytic malaria vaccines that induce high-titer, durable antibody responses can potentially provide protection from infection. Here, we engineered a virus-like particle (VLP)-based vaccine targeting a recently described vulnerable epitope at the N-terminus of the central repeat region of the Plasmodium falciparum circumsporozoite protein that is recognized by the potently inhibitory monoclonal antibody L9 and show that immunization with L9 VLPs induces strong antibody responses that provide protection from blood-stage malaria in a mouse infection model.
能够诱导高滴度、持久抗体反应的红细胞前期疟疾疫苗可能会提供感染防护。在此,我们构建了一种基于病毒样颗粒(VLP)的疫苗,该疫苗靶向恶性疟原虫环子孢子蛋白中央重复区域N端一个最近描述的易损表位,该表位可被强效抑制性单克隆抗体L9识别,并且表明用L9 VLP免疫可诱导强烈的抗体反应,在小鼠感染模型中提供针对血期疟疾的防护。