首页> 外文会议>Artificial immune systems. >In Silico Investigation into CD8Treg Mediated Recovery in Murine Experimental Autoimmune Encephalomyelitis
【24h】

In Silico Investigation into CD8Treg Mediated Recovery in Murine Experimental Autoimmune Encephalomyelitis

机译:在计算机上调查CD8Treg介导的小鼠实验性自身免疫性脑脊髓炎的恢复

获取原文
获取原文并翻译 | 示例

摘要

Experimental autoimmune encephalomyelitis (EAE) is an animal model of human autoimmune diseases in general, and multiple sclerosis (MS) in particular [2]. The animal disease is mediated through a network of cells; encephalitogenic CDThelper (CD4Thl) cells are activated in the peripheral lymph nodes following immunization for EAE, and migrate to the central nervous system where they induce activation of microglia, macrophages and dendritic cells (DCs). The resultant inflammation causes demyelination of neurons, prompting the presentation of myelin basic protein (MBP) to additional encephalitogenic T cell populations in the cervical lymph nodes by migratory DCs.
机译:实验性自身免疫性脑脊髓炎(EAE)通常是人类自身免疫性疾病的动物模型,尤其是多发性硬化症(MS)[2]。动物疾病是通过细胞网络介导的。免疫EEA后,致脑炎性CDThelper(CD4Thl)细胞在外周淋巴结中被激活,并迁移到中枢神经系统,在其中诱导小胶质细胞,巨噬细胞和树突状细胞(DC)的激活。由此产生的炎症会导致神经元脱髓鞘,从而促使迁移性DC将髓鞘碱性蛋白(MBP)呈递给子宫颈淋巴结的其他致脑性T细胞群体。

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