Role of T Cells in Experimental Spondyloarthropathy

T 细胞在实验性脊柱关节病中的作用

• 批准号: 6341706
• 负责人: JOEL D TAUROG
• 金额: $ 24.38万
• 依托单位: UT SOUTHWESTERN MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 1998
• 资助国家: 美国
• 起止时间: 1998-01-01 至 2002-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6341706
• 关键词: MHC class I antigen; antigen presentation; gene deletion mutation; gene targeting; genetically modified animals; laboratory mouse; major histocompatibility complex; molecular cloning; protein biosynthesis

HLA-B27 is a human class I MHC allele that is found with strikingly increased prevalence in patients with the rheumatic diseases termed spondyloarthropathies (SpA). There is persuasive evidence that the B27 molecule, ordinarily a normal component of the immune system, itself participates in the pathogenesis of SpA. It would represent a significant advance in the understanding of the pathogenesis of chronic idiopathic inflammatory diseases to identify the molecular role of B27 in the pathogenesis of SpA. We have developed an animal model for this disease, namely, rats transgenic for HLA-B27. These rats spontaneously develop a disease (rSpA) that in many essential ways resembles human SpA. We have previously shown that the disease in these rats is dependent upon T lymphocytes. The focus of this proposal is to gain a clearer picture of the role of these cells the disease process. In Specific Aim I, we will attempt to determine whether T cell receptor (TCR) oligoclonality is present in early lesions of the inflammatory disease in B27 transgenic rats (rSpA). The specific hypothesis to be tested is that clonal expansions of pathogenic antigen-specific T cells can be found in rats with rSpA. In Specific Aim II, we will investigate the effect of depletion of CD8 T cells on the inflammatory disease of HLA-B27 transgenic rats. In Specific Aim III, we will determine if there is an effect of a polymorphism in the gene for the peptide transporter Tap2 on peptide binding to HLA-B27 and on rSpA. These experiments will examine directly the effect of Tap2a on the B27 peptide repertoire and on disease manifestations.

HLA-B27是人类I类MHC等位基因，其在被称为脊柱关节病（SpA）的风湿性疾病患者中的患病率显著增加。 有令人信服的证据表明，B27分子，通常是免疫系统的正常组成部分，本身参与了SpA的发病机制。 明确B27在SpA发病机制中的分子作用将是理解慢性特发性炎症性疾病发病机制的重要进展。 我们已经开发了这种疾病的动物模型，即HLA-B27转基因大鼠。 这些大鼠自发地发展出一种在许多基本方面类似于人类SpA的疾病（rSpA）。 我们以前已经表明，在这些大鼠的疾病是依赖于T淋巴细胞。 这项提案的重点是更清楚地了解这些细胞在疾病过程中的作用。 在特定目标I中，我们将尝试确定是否T细胞受体（TCR）寡克隆性存在于B27转基因大鼠（rSpA）的炎症性疾病的早期病变中。 待检验的特定假设是，在rSpA大鼠中可以发现致病性抗原特异性T细胞的克隆扩增。 在特定目标II中，我们将研究CD 8 T细胞耗竭对HLA-B27转基因大鼠炎症性疾病的影响。 在特定目标III中，我们将确定肽转运蛋白Tap 2基因多态性是否对肽与HLA-B27和rSpA的结合有影响。 这些实验将直接检查Tap 2a对B27肽库和疾病表现的影响。