MHC tetramers for epitopes of B anthracis PA
MHC tetramers for epitopes of B anthracis PA
批准号:
6763899
负责人:
GERALD T NEPOM
金额:
$35.1万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-05-01 至 2006-04-30
关键词:
Bacillus anthracisanthraxanthrax vaccinesbacterial antigensbiomarkerbioterrorism /chemical warfarecellular immunityclinical researchgenetically modified animalshelper T lymphocytehuman subjectimmune responselaboratory mousemajor histocompatibility complexpatient oriented researchvaccine developmentvaccine evaluation
中文摘要
描述(由申请人提供):美国已承诺为大量人员接种炭疽疫苗。然而,人们普遍认识到目前炭疽疫苗的局限性,并正在努力改进疫苗配方。我们将创建对炭疽疫苗接种反应的生物标记和预测因子,以设计更安全、更有效的疫苗作为长期临床目标。为了实现这一目标,我们将开发新的人类II类MHC四聚体,用于识别炭疽芽孢杆菌保护性抗原(BAPA)特异性CD4+ T细胞。炭疽疫苗接种后四聚体阳性T细胞的定量和表型将作为细胞免疫的指标进行评估。
英文摘要
DESCRIPTION (provided by applicant): A commitment has been made in the USA to vaccinate large numbers of persons against anthrax. However, limitations of the current anthrax vaccine are widely acknowledged, and efforts are underway to improve the vaccine formulation. We will create biological markers and predictors of the response to anthrax vaccination, with the long-term clinical goal of designing safer and more effective vaccines. To achieve this objective, we will develop novel human class II MHC tetramers which identify antigen-specific CD4+ T cells specific for bacillus anthrax Protective Antigen (BAPA). Quantitation and phenotyping of the tetramer-positive T cells following anthrax vaccination will be evaluated as an indicator of cellular immunity.
The Specific Aims are:
Aim 1. To identify immunodominant epitopes of bacillus anthrax Protective Antigen (BAPA) based on HLA class II binding and recognized by CD4 T cells which are capable of eliciting robust immunity.
Aim 2. To use soluble HLA-BAPA tetramers to quantify the CD4 T cell response to anthrax vaccination.
Tetramers will be produced and evaluated which encompass most of the prevalent human class II haplotypes, based on selection of peptides corresponding to T cell recognition of a restricted set of BAPA epitopes. MHC-peptide binding assays, tetramer production and testing methods, and epitope scanning technologies for this project are all validated, and preliminary data using transgenic murine surrogates for the T cell response to BAPA demonstrate successful detection of the responding antigen-specific population following vaccination.
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