Dual Mechanisms for Balancing Th17 and Treg Cell Fate by CREB
- PMID: 29129697
- PMCID: PMC5704069
- DOI: 10.1016/j.ebiom.2017.10.031
Dual Mechanisms for Balancing Th17 and Treg Cell Fate by CREB
Abstract
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.
Keywords: CREB; Regulatory T cells; Th17 cells.
Copyright © 2017 The Authors. Published by Elsevier B.V. All rights reserved.
Comment on
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The dichotomous nature of T helper 17 cells.Nat Rev Immunol. 2017 Sep;17(9):535-544. doi: 10.1038/nri.2017.50. Epub 2017 May 30. Nat Rev Immunol. 2017. PMID: 28555673 Review.
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Cyclic AMP-Responsive Element-Binding Protein (CREB) is Critical in Autoimmunity by Promoting Th17 but Inhibiting Treg Cell Differentiation.EBioMedicine. 2017 Nov;25:165-174. doi: 10.1016/j.ebiom.2017.10.010. Epub 2017 Oct 12. EBioMedicine. 2017. PMID: 29050947 Free PMC article.
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