摘要
获得性再生障碍性贫血(AA)是由自身反应性 T 细胞介导的骨髓衰竭性疾病,调节性 T 细胞是一类具有免疫抑制性和免疫无能性的 T 细胞亚群,对自身反应性 T 细胞的发生和发展起关键作用,其中最重要的是 CD4+CD25+调节性 T 细胞,在自身免疫耐受和维持机体内环境稳定中至关重要,而转录因子 Foxp3是 CD4+CD25+调节性 T 细胞发育和发挥免疫功能的关键。近年来发现 AA 患者中存在CD4+CD25+Foxp3+调节性 T 细胞数量和功能的异常,CD4+CD25+Foxp3+调节性 T 细胞在 AA 发生发展中的作用及机制成为当前研究的热点,其在 AA 患者中的临床意义也日趋重要。
Acquired aplastic anemia(AA) is a disease of bone marrow failure mediated by autoimmune T cells. CD4+CD25+ regulatory T cells, which have immunosuppressive and anergic, belong to a subpopulation of T cells specialized for immune regulation and play important roles in the development of autoimmune T cells. Foxp3 plays a significant role in the development and function of regulatory T cells which have been confirmed by many investigations. In recent years, the relationship between CD4 +CD25 +Foxp3 + regulatory T cells and AA has become a hot spot of research. What’s more, its clinical significance is becoming more and more obvious in AA.
出处
《白血病.淋巴瘤》
CAS
2016年第7期438-441,共4页
Journal of Leukemia & Lymphoma
基金
国家自然科学基金(30950015)
山西省留学回国人员重点科研项目(2009-5)