Induction of regulatory T cells and dominant tolerance by dendritic cells incapable of full activation.

Transplants tolerated through a process known as infectious tolerance evoke continuous recruitment of regulatory T (Treg) cells that are necessary to maintain the unresponsive state. This state is maintained long-term and requires continuous Ag exposure. It is not known, however, whether infectious...

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Main Authors: Yates, S, Paterson, A, Nolan, K, Cobbold, S, Saunders, N, Waldmann, H, Fairchild, P
Format: Journal article
Language:English
Published: 2007
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author Yates, S
Paterson, A
Nolan, K
Cobbold, S
Saunders, N
Waldmann, H
Fairchild, P
author_facet Yates, S
Paterson, A
Nolan, K
Cobbold, S
Saunders, N
Waldmann, H
Fairchild, P
author_sort Yates, S
collection OXFORD
description Transplants tolerated through a process known as infectious tolerance evoke continuous recruitment of regulatory T (Treg) cells that are necessary to maintain the unresponsive state. This state is maintained long-term and requires continuous Ag exposure. It is not known, however, whether infectious tolerance operates through sustained recruitment of pre-existing regulatory cells, induction of regulatory cells, or both. Using mice deficient in natural Treg cells, we show here that quiescent donor dendritic cells (DC) laden with histocompatibility Ag can induce Treg cells de novo that mediate transplantation tolerance. In contrast, fully activated DC fail to do so. These findings suggest that DC incapable of delivering full activation signals to naive T cells may favor their polarization toward a regulatory phenotype. Furthermore, they suggest a role for quiescent endogenous DC in the maintenance of the tolerant state.
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spelling oxford-uuid:cd6ca3ca-0367-4fe0-be1a-d1d732fa7b2a2022-03-27T07:28:39ZInduction of regulatory T cells and dominant tolerance by dendritic cells incapable of full activation.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:cd6ca3ca-0367-4fe0-be1a-d1d732fa7b2aEnglishSymplectic Elements at Oxford2007Yates, SPaterson, ANolan, KCobbold, SSaunders, NWaldmann, HFairchild, PTransplants tolerated through a process known as infectious tolerance evoke continuous recruitment of regulatory T (Treg) cells that are necessary to maintain the unresponsive state. This state is maintained long-term and requires continuous Ag exposure. It is not known, however, whether infectious tolerance operates through sustained recruitment of pre-existing regulatory cells, induction of regulatory cells, or both. Using mice deficient in natural Treg cells, we show here that quiescent donor dendritic cells (DC) laden with histocompatibility Ag can induce Treg cells de novo that mediate transplantation tolerance. In contrast, fully activated DC fail to do so. These findings suggest that DC incapable of delivering full activation signals to naive T cells may favor their polarization toward a regulatory phenotype. Furthermore, they suggest a role for quiescent endogenous DC in the maintenance of the tolerant state.
spellingShingle Yates, S
Paterson, A
Nolan, K
Cobbold, S
Saunders, N
Waldmann, H
Fairchild, P
Induction of regulatory T cells and dominant tolerance by dendritic cells incapable of full activation.
title Induction of regulatory T cells and dominant tolerance by dendritic cells incapable of full activation.
title_full Induction of regulatory T cells and dominant tolerance by dendritic cells incapable of full activation.
title_fullStr Induction of regulatory T cells and dominant tolerance by dendritic cells incapable of full activation.
title_full_unstemmed Induction of regulatory T cells and dominant tolerance by dendritic cells incapable of full activation.
title_short Induction of regulatory T cells and dominant tolerance by dendritic cells incapable of full activation.
title_sort induction of regulatory t cells and dominant tolerance by dendritic cells incapable of full activation
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