首页> 外文期刊>Journal of Neuroimmunology: Official Bulletin of the Research Committee on Neuroimmunology of the World Federation of Neurology >Multiple sclerosis: a study of CXCL10 and CXCR3 co-localization in the inflamed central nervous system.
【24h】

Multiple sclerosis: a study of CXCL10 and CXCR3 co-localization in the inflamed central nervous system.

机译:多发性硬化症:CXCL10和CXCR3在发炎的中枢神经系统中共定位的研究。

获取原文
获取原文并翻译 | 示例
           

摘要

T-cell accumulation in the central nervous system (CNS) is considered crucial to the pathogenesis of multiple sclerosis (MS). We found that the majority of T cells within the cerebrospinal fluid (CSF) compartment expressed the CXC chemokine receptor 3 (CXCR), independent of CNS inflammation. Quantitative immunohistochemistry revealed continuous accumulation of CXCR3+ T cells during MS lesion formation. The expression of one CXCR3 ligand, interferon (IFN)-gamma-inducible protein of 10 kDa (IP-10)/CXC chemokine ligand (CXCL) 10 was elevated in MS CSF, spatially associated with demyelination in CNS tissue sections and correlated tightly with CXCR3 expression. These data suggest a critical role for CXCL10 and CXCR3 in the accumulation of T cells in the CNS of MS patients.
机译:T细胞在中枢神经系统(CNS)中的积累被认为对多发性硬化症(MS)的发病机制至关重要。我们发现脑脊液(CSF)隔室内的大多数T细胞表达CXC趋化因子受体3(CXCR),独立于中枢神经系统炎症。定量免疫组化显示MS病变形成过程中CXCR3 + T细胞不断积累。一种CXCR3配体,干扰素(IFN)-γ诱导型10 kDa(IP-10)/ CXC趋化因子配体(CXCL)10的表达在MS CSF中升高,在空间上与CNS组织切片中的脱髓鞘相关,并与CXCR3表达。这些数据表明CXCL10和CXCR3在MS患者中枢神经系统中T细胞积累中起着关键作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号