循环Tfh细胞促进B细胞活化在多发性硬化病理过程中的作用机制研究

项目名称： 循环Tfh细胞促进B细胞活化在多发性硬化病理过程中的作用机制研究

项目编号： No.31200665

项目类型： 青年科学基金项目

立项/批准年度： 2013

项目学科： 免疫学

项目作者： 郭俊

作者单位： 中国人民解放军第四军医大学

项目金额： 25万元

中文摘要： 多发性硬化（MS）作为中枢神经系统自身免疫性疾病，确切发病机制尚不明了。传统观点认为髓鞘反应性T细胞免疫介导了MS发病，新近证据支持B细胞免疫在MS中具有重要作用，但B细胞活化的调控机制尚不完全清楚。 辅助B细胞活化的主要效应细胞是滤泡辅助性T细胞（Tfh），定位于淋巴滤泡，在B细胞活化、生发中心(GC)形成及高亲和力抗体产生中发挥核心作用。研究表明外周血CD4+CXCR5+T细胞具有与Tfh相似的表型和功能，称为循环Tfh，可间接反映Tfh的功能状态。我们前期研究发现MS患者复发期外周血CD4+CXCR5+T细胞比例明显高于健康对照组，但该群细胞在MS发病中的作用如何尚无报道。 本项目采用免疫磁珠+流式细胞分选MS不同病程阶段的循环Tfh，分析其表面分子表达情况及与疾病负荷的相关性；体外细胞培养验证其对B细胞的活化作用；观察过继转移循环Tfh对EAE发病的影响，为MS治疗提供新的作用靶点

中文关键词： 滤泡辅助性T细胞；多发性硬化；实验性自身免疫性脑脊髓炎；B细胞；活化

英文摘要： Multiple sclerosis (MS) is an autoimmune disease of the central nervous system (CNS) in which the exact pathogenesis is unclear. It has been generally accepted that myelin-reactive T cell-induced immune responses cause the onset of MS, but the recent evidence has supported a critical role of B cells. However,the regulatory mechanism of the B-cell activation is not fully understood. T follicular helper (Tfh) cells, located in the lymphoid follicles, are the effector cells of B-cell activation,and play a central role in the activation of B cells,the formation of germinal center (GC) and the production of high-affinity antibodies. It has been demonstrated that CD4+CXCR5+ T cells in the peripheral blood posses a similar phenotype and function with GC-Tfh cells. In our recent study, a significant increase of circulating CD4+CXCR5+ T cells has been observed compared with healthy controls, but there is no studies concerning the potential role of these cells in the MS. In this study, we are planning to collect the circulating Tfh cells during relapsing or remitting period of RRMS patients by utilizing immunomagnetic beads and flow cytometry (FACS), evaluate the expression of the specific surface molecules, and explore the correlation between circulating Tfh cells and the disease load. We are trying to test the potential

英文关键词： T follicular helper cells；multiple sclerosis；experimental autoimmune encephalomyelitis；B cells；activation