Salmond, R orcid.org/0000-0002-1807-1056 (2023) Regulation of T cell activation and metabolism by Transforming Growth Factor-Beta. Biology, 12 (2). 297. ISSN 2079-7737
Abstract
Transforming growth factor beta (TGFβ) receptor signalling regulates T cell development, differentiation and effector function. Expression of the immune-associated isoform of this cytokine, TGFβ1, is absolutely required for the maintenance of immunological tolerance in both mice and humans, whilst context-dependent TGFβ1 signalling regulates the differentiation of both anti- and pro-inflammatory T cell effector populations. Thus, distinct TGFβ-dependent T cell responses are implicated in the suppression or initiation of inflammatory and autoimmune diseases. In cancer settings, TGFβ signals contribute to the blockade of anti-tumour immune responses and disease progression. Given the key functions of TGFβ in the regulation of immune responses and the potential for therapeutic targeting of TGFβ-dependent pathways, the mechanisms underpinning these pleiotropic effects have been the subject of much investigation. This review focuses on accumulating evidence suggesting that modulation of T cell metabolism represents a major mechanism by which TGFβ influences T cell immunity.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2023 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
Keywords: | T cell activation; immunometabolism; cytokines; signaling; TGFβ |
Dates: |
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Institution: | The University of Leeds |
Funding Information: | Funder Grant number Cancer Research UK Supplier No: 138573 C55663/A23269 |
Depositing User: | Symplectic Publications |
Date Deposited: | 23 Feb 2023 11:13 |
Last Modified: | 23 Feb 2023 11:13 |
Status: | Published |
Publisher: | MDPI |
Identification Number: | 10.3390/biology12020297 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:196712 |