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Dual Mechanisms for Balancing Th17 and Treg Cell Fate by CREB

机译:CREB平衡Th17和Treg细胞命运的双重机制

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摘要

Th17 cells, which express the cytokine IL-17A, and master regulator RORγt, are important in the inflammatory response to fungal and bacterial pathogens, but also have a pathogenic role in many inflammatory disorders. In contrast, regulatory T cells (Treg), expressing the Foxp3 transcription factor, have a suppressive function and can dampen an immune response. The appropriate balance of these distinct effector functions is critical for an effective immune response and autoimmunity can arise if this process goes awry. In this issue, Wang et al. demonstrate a critical role for the transcription factor CREB (cyclic AMP-responsive element binding protein) in regulating the balance between inflammatory Th17 and suppressive Treg cells with implications for autoimmunity.
机译:表达细胞因子IL-17A和主调节因子RORγt的Th17细胞在对真菌和细菌病原体的炎症反应中很重要,但在许多炎症性疾病中也具有致病作用。相反,表达Foxp3转录因子的调节性T细胞(Treg)具有抑制功能,可以抑制免疫反应。这些独特的效应子功能的适当平衡对于有效的免疫反应至关重要,如果此过程出错,则会产生自身免疫。在本期中,Wang等。证明转录因子CREB(环状AMP应答元件结合蛋白)在调节炎症性Th17细胞与抑制性Treg细胞之间的平衡中起着至关重要的作用,对自身免疫具有影响。

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