FOXP3型
自身免疫
免疫学
背景(考古学)
调节性T细胞
移植
生物
T细胞
医学
免疫系统
白细胞介素2受体
内科学
古生物学
作者
Anne M. Pesenacker,Laura Cook,Megan K. Levings
标识
DOI:10.1016/j.coi.2016.07.004
摘要
FOXP3 controls the development and function of T regulatory cells (Tregs). Autoimmunity is linked to changes in FOXP3 activity that can occur at multiple levels and lead to Treg dysfunction. For example, changes in IL-2 signaling, FOXP3 transcription and/or post-translational modifications can all contribute to loss of self-tolerance. As additional pathways of FOXP3 regulation are elucidated, new therapeutic approaches to increase Treg activity either by cell therapy or pharmacological intervention are being tested. Early success from pioneering studies of Treg-based therapy in transplantation has promoted the undertaking of similar studies in autoimmunity, with emerging evidence for the effectiveness of these approaches, particularly in the context of type 1 diabetes.
科研通智能强力驱动
Strongly Powered by AbleSci AI