Infectious tolerance via the consumption of essential amino acids and mTOR signaling.

Infectious tolerance describes the process of CD4(+) regulatory T cells (Tregs) converting naïve T cells to become additional Tregs. We show that antigen-specific Tregs induce, within skin grafts and dendritic cells, the expression of enzymes that consume at least 5 different essential amino acids (...

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Main Authors: Cobbold, S, Adams, E, Farquhar, C, Nolan, K, Howie, D, Lui, K, Fairchild, P, Mellor, A, Ron, D, Waldmann, H
Format: Journal article
Language:English
Published: 2009
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author Cobbold, S
Adams, E
Farquhar, C
Nolan, K
Howie, D
Lui, K
Fairchild, P
Mellor, A
Ron, D
Waldmann, H
author_facet Cobbold, S
Adams, E
Farquhar, C
Nolan, K
Howie, D
Lui, K
Fairchild, P
Mellor, A
Ron, D
Waldmann, H
author_sort Cobbold, S
collection OXFORD
description Infectious tolerance describes the process of CD4(+) regulatory T cells (Tregs) converting naïve T cells to become additional Tregs. We show that antigen-specific Tregs induce, within skin grafts and dendritic cells, the expression of enzymes that consume at least 5 different essential amino acids (EAAs). T cells fail to proliferate in response to antigen when any 1, or more, of these EAAs are limiting, which is associated with a reduced mammalian target of rapamycin (mTOR) signaling. Inhibition of the mTOR pathway by limiting EAAs, or by specific inhibitors, induces the Treg-specific transcription factor forkhead box P3, which depends on both T cell receptor activation and synergy with TGF-beta.
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spelling oxford-uuid:d57c9241-026c-44bf-96dc-908cafb48f2a2022-03-27T08:26:20ZInfectious tolerance via the consumption of essential amino acids and mTOR signaling.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:d57c9241-026c-44bf-96dc-908cafb48f2aEnglishSymplectic Elements at Oxford2009Cobbold, SAdams, EFarquhar, CNolan, KHowie, DLui, KFairchild, PMellor, ARon, DWaldmann, HInfectious tolerance describes the process of CD4(+) regulatory T cells (Tregs) converting naïve T cells to become additional Tregs. We show that antigen-specific Tregs induce, within skin grafts and dendritic cells, the expression of enzymes that consume at least 5 different essential amino acids (EAAs). T cells fail to proliferate in response to antigen when any 1, or more, of these EAAs are limiting, which is associated with a reduced mammalian target of rapamycin (mTOR) signaling. Inhibition of the mTOR pathway by limiting EAAs, or by specific inhibitors, induces the Treg-specific transcription factor forkhead box P3, which depends on both T cell receptor activation and synergy with TGF-beta.
spellingShingle Cobbold, S
Adams, E
Farquhar, C
Nolan, K
Howie, D
Lui, K
Fairchild, P
Mellor, A
Ron, D
Waldmann, H
Infectious tolerance via the consumption of essential amino acids and mTOR signaling.
title Infectious tolerance via the consumption of essential amino acids and mTOR signaling.
title_full Infectious tolerance via the consumption of essential amino acids and mTOR signaling.
title_fullStr Infectious tolerance via the consumption of essential amino acids and mTOR signaling.
title_full_unstemmed Infectious tolerance via the consumption of essential amino acids and mTOR signaling.
title_short Infectious tolerance via the consumption of essential amino acids and mTOR signaling.
title_sort infectious tolerance via the consumption of essential amino acids and mtor signaling
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