首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Costimulation of memory T-cells by ICOS: a potential therapeutic target for autoimmunity?
【24h】

Costimulation of memory T-cells by ICOS: a potential therapeutic target for autoimmunity?

机译:ICOS对记忆性T细胞的共刺激:自身免疫的潜在治疗靶点?

获取原文
获取原文并翻译 | 示例
           

摘要

Approaches that target costimulatory receptors are independent of T-cell receptor specificity and may be useful for T-cell-mediated diseases in which the antigens involved are not well defined. However, the proper costimulatory pathways need to be targeted. For example, therapies for human T-cell-mediated diseases need to be effective against previously activated memory cells. In this review, we use autoimmune demyelination as a paradigm for established immune-mediated pathogenesis. Studies with the human disease multiple sclerosis and the rodent model experimental autoimmune encephalomyelitis have suggested that the effectiveness of CD28 blockade, as a therapeutic strategy for established autoimmune demyelination, may be limited. ICOS, a receptor that appears to be involved in the costimulation of previously activated T-cells, may be an attractive alternative. Copyright 2001 Academic Press.
机译:靶向共刺激受体的方法不依赖于T细胞受体特异性,对于未明确定义所涉及抗原的T细胞介导疾病可能有用。但是,需要确定适当的共刺激途径。例如,用于人类T细胞介导的疾病的疗法需要有效对抗先前激活的记忆细胞。在这篇综述中,我们使用自身免疫脱髓鞘作为建立的免疫介导的发病机制的范例。对人类疾病多发性硬化症和啮齿动物模型实验性自身免疫性脑脊髓炎的研究表明,CD28阻断作为已建立的自身免疫性脱髓鞘的治疗策略的有效性可能受到限制。 ICOS是一种可能参与先前激活的T细胞共刺激的受体,可能是一种有吸引力的选择。版权所有2001,学术出版社。

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