Salinas Nichole D, Ma Rui, McAleese Holly, Ouahes Tarik, Long Carole A, Miura Kazutoyo, Lambert Lynn E, Tolia Niraj H
Host-Pathogen Interactions and Structural Vaccinology Section, Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Vaccine Development Unit, Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Vaccines (Basel). 2024 May 16;12(5):546. doi: 10.3390/vaccines12050546.
Malaria is caused by eukaryotic protozoan parasites of the genus . There are 249 million new cases and 608,000 deaths annually, and new interventions are desperately needed. Malaria vaccines can be divided into three categories: liver stage, blood stage, or transmission-blocking vaccines. Transmission-blocking vaccines prevent the transmission of disease by the mosquito vector from one human to another. Pfs230 is one of the leading transmission-blocking vaccine antigens for malaria. Here, we describe the development of a 24-copy self-assembling nanoparticle vaccine comprising domain 1 of Pfs230 genetically fused to ferritin. The single-component Pfs230D1-ferritin construct forms a stable and homogenous 24-copy nanoparticle with good production yields. The nanoparticle is highly immunogenic, as two low-dose vaccinations of New Zealand White rabbits elicited a potent and durable antibody response with high transmission-reducing activity when formulated in two distinct adjuvants suitable for translation to human use. This single-component 24-copy Pfs230D1-ferritin nanoparticle vaccine has the potential to improve production pipelines and the cost of manufacturing a potent and durable transmission-blocking vaccine for malaria control.
疟疾由疟原虫属的真核原生动物寄生虫引起。每年有2.49亿新发病例和60.8万人死亡,因此迫切需要新的干预措施。疟疾疫苗可分为三类:肝期疫苗、血期疫苗或传播阻断疫苗。传播阻断疫苗可防止蚊媒将疾病从一个人传播给另一个人。Pfs230是主要的疟疾传播阻断疫苗抗原之一。在此,我们描述了一种由Pfs230的结构域1与铁蛋白基因融合而成的24拷贝自组装纳米颗粒疫苗的研发情况。单组分Pfs230D1-铁蛋白构建体形成了一种稳定且均匀的24拷贝纳米颗粒,产量很高。该纳米颗粒具有高度免疫原性,因为对新西兰白兔进行两次低剂量接种时,在两种适合转化为人类使用的不同佐剂中配制后,会引发强烈且持久的抗体反应,并具有高传播减少活性。这种单组分24拷贝Pfs230D1-铁蛋白纳米颗粒疫苗有潜力改善生产流程,并降低制造一种有效且持久的疟疾传播阻断疫苗的成本。