Functional analysis of erythrocyte determinants of malaria infection

疟疾感染红细胞决定因素的功能分析

• 批准号: 8645599
• 负责人: Manoj T Duraisingh
• 金额: $ 40.38万
• 依托单位: HARVARD SCHOOL OF PUBLIC HEALTH
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-05-01 至 2016-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8645599
• 关键词: Affect; Anti-malarial drug resistance; Antimalarials; Binding Proteins; Biochemical; Biological; Blood Circulation; Blood Group Antigens; Blood typing procedure; Cell surface; Cessation of life; Childhood; Clinical; Communicable Diseases; Development; Disease; Drug resistance; Environment; Erythrocytes; Gene Targeting; Genes; Genetic; Genetic Polymorphism; Genetic Screening; Glycophorin A; Goals; Growth; Hematopoietic stem cells; Homologous Protein; Human; Human Pathology; Immune; In Vitro; Individual; Infection; Intervention; Knock-out; Lead; Life; Ligands; Malaria; Measures; Membrane Proteins; Molecular Genetics; Parasites; Pathway interactions; Pharmaceutical Preparations; Plasmodium falciparum; Play; Population; Process; Proteins; RNA Interference; Regimen; Relative (related person); Resources; Reticulocytes; Role; Stem cells; Subfamily lentivirinae; Surface; System; Vaccines; Variant; Work; antigen binding; base; blood group; combinatorial; design; erythrocyte receptor; genetic analysis; loss of function; loss of function mutation; member; mortality; mutant; novel; novel strategies; novel therapeutics; parasite invasion; positional cloning; public health relevance; receptor; response; therapeutic target; vaccine candidate; vaccine development

DESCRIPTION (provided by applicant): Malaria remains a major global infectious disease, largely affecting people living in resource poor environments, and is one of the most important causes of childhood mortality. Drug-resistance is constantly undermining the usefulness of antimalarial regimens. There is an urgent need for the development of new therapeutic strategies. Plasmodium falciparum parasites utilize multiple ligand-receptor interactions for the invasion of human erythrocytes. Much work has focused on the characterization of parasite ligands, with the goal of developing them as vaccine candidates. Largely due to the genetic intractabiliy of enucleated human erythrocytes, the function of host human erythrocyte receptors in ligand-receptor interactions has not been comprehensively assessed. We have developed an approach combining an in vitro erythrocyte culture system, which supports P. falciparum invasion and growth, with lentiviral transduction to generate genetically modified erythrocytes. The best characterized ligand-receptor interaction in P. falciparum is that of the ligand EBA-175 and its receptor glycophorin A, with EBA-175 being developed as a vaccine candidate. Using this system, we have achieved knockdown in expression of glycophorin A, genetically demonstrating that it is required for efficient strain-specific parasite invasion. We hypothesize that targeting a limited number of erythrocyte receptors will be sufficient to abrogate P. falciparum invasion in all P. falciparum parasite lines. This project will functionally analyze erythrocyte determinants of the invasion process of P. falciparum. We will use 1) a loss-of- function approach to establish a hierarchy amongst putative erythrocyte receptors for invasion, 2) a combinatorial knockdown approach to identify minimal sets of erythrocyte surface determinants that are essential for invasion and 3) a genetic screen to identify human blood group antigens that are novel determinants of invasion. In the long-term we hope that our studies will provide a functional understanding of critical ligand-receptor interactions for P. falciparum invasion of erythrocytes to inform vaccine development and the design of host-targeted therapeutics.

描述（由申请人提供）：疟疾仍然是一种主要的全球性传染病，主要影响生活在资源贫乏环境中的人们，并且是儿童死亡的最重要原因之一。抗药性不断破坏抗疟疗法的效用。迫切需要开发新的治疗策略。恶性疟原虫寄生虫利用多种配体-受体相互作用侵入人类红细胞。许多工作都集中在寄生虫配体的表征，其目标是将其开发为候选疫苗。主要由于去核人红细胞的遗传不稳定性，尚未全面评估宿主人红细胞受体在配体-受体相互作用中的功能。我们已经开发了一种方法，该方法将支持恶性疟原虫侵袭和生长的体外红细胞培养系统与慢病毒转导相结合，以产生遗传修饰的红细胞。恶性疟原虫中最具特征的配体-受体相互作用是配体EBA-175及其受体血型糖蛋白A的相互作用，EBA-175被开发为候选疫苗。使用该系统，我们已经实现了血型糖蛋白A表达的敲低，遗传上证明了它是有效的菌株特异性寄生虫入侵所必需的。我们假设靶向有限数量的红细胞受体将足以消除所有恶性疟原虫寄生虫系中的恶性疟原虫入侵。本项目将对恶性疟原虫侵袭过程中的红细胞决定因子进行功能分析。我们将使用1）功能丧失的方法来建立一个层次之间的推定红细胞受体的入侵，2）组合敲低的方法来确定最小集的红细胞表面决定因素是必不可少的入侵和3）遗传筛选，以确定人类血型抗原是新的入侵决定因素。从长远来看，我们希望我们的研究将提供对恶性疟原虫入侵红细胞的关键配体-受体相互作用的功能性理解，以告知疫苗开发和宿主靶向疗法的设计。