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Characterization of Human T Cells Against Chlamydia

人类 T 细胞抗衣原体的特性

基本信息

批准号：
7414396
负责人：
Paula B. Kavathas
金额：
$ 34.22万
依托单位：
YALE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2004
资助国家：
美国
起止时间：
2004-05-01 至 2010-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7414396
关键词：
Alleles Antibodies Antigen-Presenting Cells Antigens Applications Grants Bacterial Sexually Transmitted Diseases Biological Assay Blood CD4 Positive T Lymphocytes CD8B1 gene CTL assay Cell surface Cells Characteristics Chlamydia Chlamydia trachomatis Chlamydophila pneumoniae Chlamydophila psittaci Chronic Class Common Epitope Complement Effectiveness Epitope Mapping Epitopes Frequencies Future Goals HLA Antigens Histocompatibility Antigens Class II Homologous Protein Human Immune response Immunity Immunization Individual Infection Infertility Inflammation Interferon Type II Laboratories Location MHC Class I Genes Membrane Membrane Proteins Mothers Newborn Infant Numbers Organism Outcome Pathway interactions Pelvis Peptides Protein Region Proteins Recombinants Risk Set protein T-Lymphocyte T-Lymphocyte Epitopes Testing Vaccines Virus Diseases Woman antigen processing bacterial H antigen base cytokine cytotoxic cytotoxicity exhaust granzyme B immunogenic lymphoblastoid cell line major outer membrane protein mutant response vaccine development

项目摘要

DESCRIPTION (provided by applicant): Chlamydia trachomatis (Ct) is the most common cause of bacterial sexually transmitted disease worldwide. In the majority of infected individuals they are asymptomatic. This poses a heath risk for women, causing pelvic inflammation and tubal infertility, and for newborns from infected mothers. Our goal is to characterize the human T cell immune response to Ct in infected individuals with the goal of identifying immunogenic proteins and peptides that could be used for vaccine development. We will determine whether CD4 or CD8 T cell responses can be elicited against Ct proteins that enter the MHC class I or class II antigen processing pathway or are likely to enter those pathways. Specific peptide epitopes from these proteins and the HLA allotypes that present the peptides will be determined using a unique panel of B lymphoblastoid lines expressing single HLA antigens. Our hypothesis is that some regions of immunogenic proteins will contain epitope clusters for both CD4 and CD8 T cells as we found for the major outer membrane protein MOMP. The functional characteristics of the Ct-specific T cells will be determined using antibodies against cytokines, proteins involved in cytotoxicity, and cell surface molecules. Assays such as the Lysispot assay will be used to determine CTL function. Ct-specific T cells in the blood of infected individuals will be enumerated with MHC class I tetramer and class II tetramers. We will determine if the CD8 T cells recognizing Ct antigens are functional CTL cells or potentially "exhausted" T cells lacking CTL activity, which has been found in chronic viral infections. The potential for immunogenic epitopes to cross-protect other Ct species such as C. pneumonia and C. psittaci will be determined by sequence comparisons. Characterizing human T cell responses to Ct is important for understanding immunity to Ct in humans and for future vaccine development.

描述（由申请人提供）：沙眼衣原体（Ct）是全球细菌性传播疾病的最常见原因。大多数感染者没有症状。这对妇女和受感染母亲的新生儿构成健康风险，导致盆腔炎和输卵管不孕。我们的目标是表征感染个体中对Ct的人T细胞免疫应答，目的是鉴定可用于疫苗开发的免疫原性蛋白质和肽。我们将确定是否可以针对进入MHC I类或II类抗原加工途径或可能进入这些途径的Ct蛋白引起CD4或CD8 T细胞应答。来自这些蛋白质的特异性肽表位和呈递肽的HLA同种异型将使用表达单一HLA抗原的一组独特的B类淋巴母细胞系来确定。我们的假设是，免疫原性蛋白质的一些区域将包含CD4和CD8 T细胞的表位簇，正如我们发现的主要外膜蛋白MOMP。Ct特异性T细胞的功能特征将使用针对细胞因子、参与细胞毒性的蛋白质和细胞表面分子的抗体来确定。将使用诸如Lysispot测定的测定来确定CTL功能。感染个体血液中的Ct特异性T细胞将用MHC I类四聚体和II类四聚体计数。我们将确定识别Ct抗原的CD8 T细胞是功能性CTL细胞还是缺乏CTL活性的潜在“耗竭”T细胞，这在慢性病毒感染中已被发现。免疫原性表位交叉保护其他Ct物种如C.肺炎和C.将通过序列比较来确定鹦鹉热。表征人类T细胞对Ct的反应对于理解人类对Ct的免疫力和未来的疫苗开发是重要的。

项目成果

期刊论文数量（4）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Uric acid induces trophoblast IL-1β production via the inflammasome: implications for the pathogenesis of preeclampsia.

DOI：
10.1111/j.1600-0897.2010.00960.x
发表时间：
2011-06
期刊：
American journal of reproductive immunology (New York, N.Y. : 1989)
影响因子：
0
作者：
Mulla MJ;Myrtolli K;Potter J;Boeras C;Kavathas PB;Sfakianaki AK;Tadesse S;Norwitz ER;Guller S;Abrahams VM
通讯作者：
Abrahams VM

Chlamydia trachomatis infection modulates trophoblast cytokine/chemokine production.