Modular Chimeric Vaccines tailored for malaria parasites

针对疟疾寄生虫量身定制的模块化嵌合疫苗

• 批准号: 7468359
• 负责人: Alberto Moreno
• 金额: $ 40.25万
• 依托单位: EMORY UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-08-15 至 2011-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7468359
• 关键词: Advanced Development; Africa; Algorithms; Amino Acid Sequence; Antibodies; Antigens; Aotus primate; Area; B-Lymphocyte Epitopes; CD4 Positive T Lymphocytes; Centers for Disease Control and Prevention (U.S.); Characteristics; Chloroquine; Clinical; Clinical Trials; Codon Nucleotides; Computer Assisted; Computer Simulation; Cytotoxic T-Lymphocytes; Data; Development; Drug Formulations; Drug resistance; Epitopes; Erythrocytes; Escherichia coli Proteins; Evaluation; Exposure to; Genes; Genetic; Goals; Gold; Health; Helper-Inducer T-Lymphocyte; Human; Immune response; Immune system; Immunity; Immunization; Infection; Infection Control; Intervention; Life Cycle Stages; Macaca mulatta; Malaria; Malaria Vaccines; Measures; Mediating; Modeling; Molecular; Molecular Conformation; Monkeys; Mus; Numbers; Parasites; Peptides; Plasmodium; Plasmodium cynomolgi; Plasmodium knowlesi; Plasmodium vivax; Primaquine; Procedures; Proteins; Recombinant Proteins; Research; Research Proposals; Sporozoites; Staging; Standards of Weights and Measures; Structure; Synthetic Genes; Synthetic Vaccines; T-Lymphocyte Epitopes; Testing; Therapeutic; Translating; Vaccine Design; Vaccines; Vivax Malaria; base; clinically relevant; design; disorder control; experience; immunogenicity; nonhuman primate; novel; novel strategies; prophylactic; research study; response; vaccine development

DESCRIPTION (provided by applicant): The overall goal of this research proposal is to optimize the design, composition and formulation of malaria Modular Chimeric Vaccines (MCVs) as effective intervention measures to control the disease in endemic areas. MCVs are synthetic genes designed to express an array of protective antigens derived from several proteins and a number of Plasmodium universal T cell epitopes. Malaria universal T cell epitopes will promote helper T-cell responses, overcome the genetic restriction associated with several malaria antigens and facilitate the boosting effect induced by natural exposure to malaria parasites. MCVs will be designed in silico using computer-assisted algorithms to predict molecular conformation and stability characteristics and to induce immune responses to several stages of the parasite life cycle. The amino acid sequences of these chimeric constructs will be reverse translated, codon optimized and assembled into synthetic genes. The synthetic genes will be cloned, inserted into E. coli, and the proteins expressed and purified. These antigens will be assessed for molecular stability and antigenicity, and then tested for immunogenicity and protection. The first specific aim will focus on developing strategies to construct and deliver stable and efficacious MCVs that can protect rhesus macaques against the experimental challenge with a simian malaria parasite Plasmodium cynomolgi. This parasite reproduces in rhesus monkeys several clinical features of the infection of humans with P. vivax. The second aim of the project will build on the experience gained to design MCVs with the potential to protect humans against P. vivax. These P. vivax MCVs will be tested for immunogenicity and protection in Aotus monkeys, a non-human primate model considered the gold standard for testing malaria vaccine candidates. Our rigorous evaluation of MCVs in stringent models of protection will provide critical data to advance the development of this vaccine platform for use in clinical trials. Relevance. Malaria caused by P. vivax is a major worldwide health problem with an estimated 80 million cases annually. Outside Africa, P. vivax is the most widely distributed malaria parasite. P. vivax malaria is resurging and now represents a serious threat in areas where it had been eradicated. The emergence of P. vivax chloroquine and primaquine drug resistant strains has brought increased emphasis to the need for alternative prophylactic and therapeutic strategies to control this infection.

描述（由申请人提供）：本研究方案的总体目标是优化疟疾模块嵌合疫苗（MCV）的设计、组成和配方，作为控制流行区疾病的有效干预措施。MCV是合成基因，其被设计为表达衍生自几种蛋白质和许多疟原虫通用T细胞表位的保护性抗原阵列。疟疾通用T细胞表位将促进辅助性T细胞应答，克服与几种疟疾抗原相关的遗传限制，并促进由自然暴露于疟原虫诱导的增强效应。MCV将使用计算机辅助算法在计算机上设计，以预测分子构象和稳定性特征，并诱导对寄生虫生命周期几个阶段的免疫反应。这些嵌合构建体的氨基酸序列将被反向翻译、密码子优化并组装成合成基因。这些合成基因将被克隆，插入到E. coli中进行表达和纯化。将评估这些抗原的分子稳定性和抗原性，然后检测免疫原性和保护性。第一个具体目标将侧重于制定策略，以构建和提供稳定有效的MCV，可以保护恒河猴免受猴疟疾寄生虫食蟹猴疟原虫的实验挑战。这种寄生虫在恒河猴中复制了人类感染间日疟原虫的几个临床特征。该项目的第二个目标将建立在设计具有保护人类免受间日疟原虫侵害潜力的MCV所获得的经验的基础上。这些间日疟原虫MCV将在Aotus猴中检测免疫原性和保护性，Aotus猴是一种非人灵长类动物模型，被认为是检测疟疾候选疫苗的金标准。我们在严格的保护模型中对MCV进行的严格评估将为推进该疫苗平台的开发提供关键数据，以用于临床试验。本案无关由间日疟原虫引起的疟疾是一个主要的世界性健康问题，估计每年有8000万病例。在非洲以外，间日疟原虫是分布最广的疟疾寄生虫。间日疟原虫疟疾正在死灰复燃，现在在已经根除的地区构成严重威胁。间日疟原虫氯喹和伯氨喹耐药菌株的出现使人们越来越重视对控制这种感染的替代预防和治疗策略的需求。