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NOVEL APPROACH TO CHLAMYDIA VACCINE DEVELOPMENT

NOVEL APPROACH TO CHLAMYDIA VACCINE DEVELOPMENT
衣原体疫苗开发的新方法
批准号:
7058323
负责人:
ELLEN KRAIG
金额:
$32.08万
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 2008-04-30

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中文摘要
翻译
描述(由申请人提供):沙眼衣原体是美国性传播疾病(STD)的主要细菌原因,并继续在人群中传播,因为> 50%的感染者没有明显症状,无法获得治疗。这些未经治疗的衣原体感染会导致严重的并发症,包括盆腔炎、输卵管不孕和宫外孕,从而对妇女造成特别的健康风险。尽管这是一个高度优先事项,但已证明很难设计出一种有效的沙眼衣原体疫苗。研究表明,T细胞是免疫保护所必需的,但它们也可能导致与发病机制相关的炎症。因此,阐明免疫T细胞在感染过程中的作用是非常重要的。虽然T细胞克隆对C.尽管已经报道了沙眼衣原体,但是很难获得足够数量的这种同质系来分析对这种病原体的T细胞应答的库(repertoire)。因此,我们已经利用T细胞杂交瘤技术,以产生克隆的辅助(CD4+)和细胞毒性(CD8+)T细胞从小鼠阴道接种有活力的沙眼衣原体的面板。T细胞杂交瘤将为我们提供一个独特的工具,用于识别抗原从C。沙眼衣原体,能够在小鼠中引发广泛的T细胞应答。此外,通过与拉克兰空军基地威尔福德霍尔医学中心的临床研究人员的新合作,将有可能评估感染衣原体的人类T细胞是否对小鼠中鉴定的相同抗原产生反应。这些目标代表了T细胞杂交瘤首次被用于评估T细胞对活衣原体感染的响应,并应提供重要的见解,以增强对衣原体的免疫力的新方法。沙眼和其他细胞内病原体。
英文摘要
DESCRIPTION (provided by applicant): Chlamydia trachomatis is the leading bacterial cause of sexually transmitted disease (STD) in the United States and continues to spread in the population as >50% of the infected individuals show no overt symptoms and fail to obtain treatment. These untreated chlamydial infections pose a particular health risk in women by leading to severe complications including pelvic inflammation, tubal infertility, and ectopic pregnancy. Although a high priority, it has proven difficult to design an effective vaccine for Chlamydia trachomatis. It has been shown that T cells are necessary for immune protection, but they may also contribute to inflammation associated with pathogenesis. Thus, it is of great importance to delineate the roles of immune T cells during infection. Although T cell clones specific for C. trachomatis have been reported, it has been difficult to obtain sufficient numbers of such homogeneous lines to analyze the repertoire of the T cell response to this pathogen. Thus, we have exploited T cell hybridoma technology in order to generate panels of cloned helper (CD4 +) and cytotoxic (CD8 +) T cells from mice that had been vaginally inoculated with viable Chlamydia trachomatis. The T cell hybridomas will provide us with a unique tool for use in identifying the antigens from C. trachomatis that are capable of eliciting a broadbased T cell response in mice. In addition, through a new collaboration with clinical investigators at Wilford Hall Medical Center, Lackland Air Force Base, it will be possible to assess whether T cells from humans infected with Chlamydia respond to the same antigens that were identified in mice. These aims represent the first time that T cell hybridomas have been used to assess the activation of T cells in response to an infection with viable Chlamydia and should provide important insights into novel approaches for enhancing immunity to C. trachomatis and to other intracellular pathogens.
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