Steel Ryan W J, Sack Brandon K, Tsuji Moriya, Navarro Mary Jane L, Betz Will, Fishbaugher Matt E, Flannery Erika L, Kappe Stefan H I
Center for Infectious Disease Research, Seattle, Washington, USA.
HIV and Malaria Vaccine Program, Aaron Diamond AIDS Research Center, New York, New York, USA.
Clin Vaccine Immunol. 2017 Feb 6;24(2). doi: 10.1128/CVI.00445-16. Print 2017 Feb.
Plasmodium falciparum malaria remains the deadliest parasitic disease worldwide. Vaccines targeting the preerythrocytic sporozoite and liver stages have the potential to entirely prevent blood-stage infection and disease, as well as onward transmission. Sporozoite surface and secreted proteins are leading candidates for inclusion in a preerythrocytic stage-specific, antibody-based vaccine. Preclinical functional assays to identify humoral correlates of protection in vitro and to validate novel sporozoite protein targets for inclusion in multisubunit vaccines currently do not consider the interaction of sporozoite-targeting antibodies with other components of the immune system. Here, we describe the development of a simple flow cytometric assay to quantitatively assess the ability of antibodies directed against P. falciparum sporozoites to facilitate their phagocytosis. We demonstrate that this sporozoite opsonic phagocytosis assay (SOPA) is compatible with both monoclonal antibodies and human immune serum and can be performed using cryopreserved P. falciparum sporozoites. This simple, accessible assay will aid with the assessment of antibody responses to vaccination with Plasmodium antigens and their interaction with phagocytic cells of the immune system.
恶性疟原虫疟疾仍然是全球最致命的寄生虫病。针对红细胞前期子孢子和肝脏阶段的疫苗有潜力完全预防血液阶段的感染和疾病,以及阻止传播。子孢子表面和分泌蛋白是红细胞前期阶段特异性抗体疫苗的主要候选成分。目前,用于在体外鉴定保护性体液相关物以及验证用于多亚基疫苗的新型子孢子蛋白靶点的临床前功能测定并未考虑靶向子孢子的抗体与免疫系统其他成分的相互作用。在此,我们描述了一种简单的流式细胞术测定方法的开发,用于定量评估针对恶性疟原虫子孢子的抗体促进其吞噬作用的能力。我们证明,这种子孢子调理吞噬作用测定法(SOPA)与单克隆抗体和人免疫血清均兼容,并且可以使用冷冻保存的恶性疟原虫子孢子进行。这种简单、易操作的测定方法将有助于评估针对疟原虫抗原疫苗接种的抗体反应及其与免疫系统吞噬细胞的相互作用。