Human T-cell Epitopes in SARS

SARS 中的人类 T 细胞表位

• 批准号: 7426937
• 负责人: Michael Joseph Buchmeier
• 金额: $ 53.53万
• 依托单位: UNIVERSITY OF CALIFORNIA-IRVINE
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-07-01 至 2010-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7426937
• 关键词: Address; Alleles; Animal Model; Animals; Antibody Formation; Binding; Bioinformatics; Biological; Biological Assay; CD4 Positive T Lymphocytes; Categories; Cells; Cellular Assay; Class; Classification; Copulation; Coronavirus; Coronavirus Infections; Data; Development; Diagnostic; Diagnostic Reagent; Disease; Epitopes; Ethnic Origin; Evaluation; General Population; Genes; Genetic Polymorphism; Genome; Goals; Helper-Inducer T-Lymphocyte; Histocompatibility Antigens Class II; Human; Ice; Immunity; In Vitro; Individual; Infection; Lead; Life; MHC binding peptide; Macaca; Modeling; Mus; Peptides; Performance; Peripheral Blood Mononuclear Cell; Play; Prevention; Primates; Range; Role; SARS coronavirus; Sampling; Severe Acute Respiratory Syndrome; System; T-Lymphocyte; T-Lymphocyte Epitopes; Testing; Time; Transgenic Mice; Transgenic Organisms; Vaccines; Vaccinia; Vaccinia virus; Validation; Viral Antigens; Virus; Work; base; cytotoxic; design; genome wide association study; immunogenic; immunogenicity; in vivo; interdisciplinary approach; mouse model; nonhuman primate; protein aminoacid sequence; research study; response; size; vaccine delivery

DESCRIPTION (provided by applicant): The discovery and validation of HLA-restricted cytotoxic and helper T cell epitopes derived from the Severe Acute Respiratory Syndrome coronavirus (SARS CoV) represents a significant challenge because of the large genome size and because of the extreme polymorphism of HLA alleles. Herein, we propose to combine bioinformatic approaches and high throughput MHC- peptide binding assays to identify epitopes restricted by HLA class I and class II molecules representative of >95% of the general population, irrespective of ethnicity. These epitopes will be further validated with in vivo and in vitro immunogenicity studies utilizing HLA transgenic mice and human PBMC from healthy unexposed donors. Animal models are likely to play a vital role in the development of SARS specific vaccines and diagnostics. Accordingly, we also plan to identify epitopes presented by mouse and human MHC molecules expressed in human MHC transgenic mice. In the final part of this application, we propose to explore development of a multi-epitope SARS vaccine construct. This construct could be utilized by itself, or in conjunction with other vaccine constructs aimed at inducing anti-SARS antibody responses. Because the proposed approach is based on a systematic definition of the immunogenic potential of SARS-derived peptide sequences, only minimal use of live SARS virus or biological samples from infected or convalescent individuals is required. The studies proposed herein will lead to the definition of a broad range of epitopes, facilitate the development of diagnostic reagents necessary to rigorously evaluate T cell responses associated with infection in humans, and enable the evaluation, at the level of T cell immunity, of the performance of different vaccine candidates.

描述（由申请人提供）：来自严重急性呼吸综合征冠状病毒（SARS CoV）的HLA限制性细胞毒性和辅助性T细胞表位的发现和验证代表了一个重大挑战，因为大基因组大小和HLA等位基因的极端多态性。在此，我们建议结合生物信息学方法和高通量MHC-肽结合测定来鉴定HLA I类和II类分子限制的表位，这些分子代表了大约95%的普通人群，而不考虑种族。这些表位将通过利用HLA转基因小鼠和来自健康未暴露供体的人PBMC进行体内和体外免疫原性研究进一步验证。动物模型可能在SARS特异性疫苗和诊断方法的开发中发挥至关重要的作用。因此，我们还计划鉴定在人MHC转基因小鼠中表达的小鼠和人MHC分子所呈现的表位。在本申请的最后一部分，我们建议探索开发一种多表位SARS疫苗结构。该构建体可以单独使用，也可以与其他旨在诱导抗sars抗体反应的疫苗构建体结合使用。由于所提出的方法是基于对SARS衍生肽序列的免疫原性潜力的系统定义，因此只需要少量使用活的SARS病毒或来自感染者或恢复期个体的生物样本。本文提出的研究将导致广泛的表位的定义，促进诊断试剂的发展，以严格评估与人类感染相关的T细胞反应，并使在T细胞免疫水平上评估不同候选疫苗的性能成为可能。