TGF-β control of adaptive immune tolerance: A break from Treg cells Journal Article


Authors: Liu, M.; Li, S.; Li, M. O.
Article Title: TGF-β control of adaptive immune tolerance: A break from Treg cells
Abstract: The vertebrate adaptive immune system has well defined functions in maintaining tolerance to self-tissues. Suppression of autoreactive T cells is dependent on the regulatory cytokine transforming growth factor-β (TGF-β) and regulatory T (Treg) cells, a distinct T cell lineage specified by the transcription factor Foxp3. Although TGF-β promotes thymic Treg (tTreg) cell development by repressing T cell clonal deletion and peripheral Treg cell differentiation by inducing Foxp3 expression, a recent study shows that TGF-β suppresses autoreactive T cells independent of Foxp3+ Treg cells. These findings imply that as an ancestral growth factor family member, TGF-β may have been co-opted as a T cell-intrinsic mechanism of self-tolerance control to assist the evolutionary transition of vertebrate adaptive immunity. Later, perhaps in placental mammals upon their acquisition of a TGF-β regulatory element in the Foxp3 locus, the TGF-β pathway is further engaged to induce peripheral Treg cell differentiation and expand the scope of T cell tolerance control to innocuous foreign antigens. © 2018 WILEY Periodicals, Inc.
Keywords: evolution; immune tolerance; autoimmunity; adaptive immunity; foxp3; tgf-β; treg
Journal Title: BioEssays
Volume: 40
Issue: 11
ISSN: 0265-9247
Publisher: John Wiley & Sons  
Date Published: 2018-11-01
Start Page: 1800063
Language: English
DOI: 10.1002/bies.201800063
PUBMED: 30159904
PROVIDER: scopus
PMCID: PMC6300063
DOI/URL:
Notes: Review -- Export Date: 1 November 2018 -- Source: Scopus
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  1. Ming Li
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  2. Ming Liu
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  3. Shun Li
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