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Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells
Regulatory T cells (Tregs) fulfill a central role in immune regulation. We reported previously that the integrin α(E)β(7) discriminates distinct subsets of murine CD4(+) regulatory T cells. Use of this marker has now helped to unravel a fundamental dichotomy among regulatory T cells. α(E) (−)CD25(+)...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211798/ https://www.ncbi.nlm.nih.gov/pubmed/14757740 http://dx.doi.org/10.1084/jem.20031562 |
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author | Huehn, Jochen Siegmund, Kerstin Lehmann, Joachim C.U. Siewert, Christiane Haubold, Uta Feuerer, Markus Debes, Gudrun F. Lauber, Joerg Frey, Oliver Przybylski, Grzegorz K. Niesner, Uwe de la Rosa, Maurus Schmidt, Christian A. Bräuer, Rolf Buer, Jan Scheffold, Alexander Hamann, Alf |
author_facet | Huehn, Jochen Siegmund, Kerstin Lehmann, Joachim C.U. Siewert, Christiane Haubold, Uta Feuerer, Markus Debes, Gudrun F. Lauber, Joerg Frey, Oliver Przybylski, Grzegorz K. Niesner, Uwe de la Rosa, Maurus Schmidt, Christian A. Bräuer, Rolf Buer, Jan Scheffold, Alexander Hamann, Alf |
author_sort | Huehn, Jochen |
collection | PubMed |
description | Regulatory T cells (Tregs) fulfill a central role in immune regulation. We reported previously that the integrin α(E)β(7) discriminates distinct subsets of murine CD4(+) regulatory T cells. Use of this marker has now helped to unravel a fundamental dichotomy among regulatory T cells. α(E) (−)CD25(+) cells expressed L-selectin and CCR7, enabling recirculation through lymphoid tissues. In contrast, α(E)-positive subsets (CD25(+) and CD25(−)) displayed an effector/memory phenotype expressing high levels of E/P-selectin–binding ligands, multiple adhesion molecules as well as receptors for inflammatory chemokines, allowing efficient migration into inflamed sites. Accordingly, α(E)-expressing cells were found to be the most potent suppressors of inflammatory processes in disease models such as antigen-induced arthritis. |
format | Text |
id | pubmed-2211798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22117982008-03-11 Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells Huehn, Jochen Siegmund, Kerstin Lehmann, Joachim C.U. Siewert, Christiane Haubold, Uta Feuerer, Markus Debes, Gudrun F. Lauber, Joerg Frey, Oliver Przybylski, Grzegorz K. Niesner, Uwe de la Rosa, Maurus Schmidt, Christian A. Bräuer, Rolf Buer, Jan Scheffold, Alexander Hamann, Alf J Exp Med Article Regulatory T cells (Tregs) fulfill a central role in immune regulation. We reported previously that the integrin α(E)β(7) discriminates distinct subsets of murine CD4(+) regulatory T cells. Use of this marker has now helped to unravel a fundamental dichotomy among regulatory T cells. α(E) (−)CD25(+) cells expressed L-selectin and CCR7, enabling recirculation through lymphoid tissues. In contrast, α(E)-positive subsets (CD25(+) and CD25(−)) displayed an effector/memory phenotype expressing high levels of E/P-selectin–binding ligands, multiple adhesion molecules as well as receptors for inflammatory chemokines, allowing efficient migration into inflamed sites. Accordingly, α(E)-expressing cells were found to be the most potent suppressors of inflammatory processes in disease models such as antigen-induced arthritis. The Rockefeller University Press 2004-02-02 /pmc/articles/PMC2211798/ /pubmed/14757740 http://dx.doi.org/10.1084/jem.20031562 Text en Copyright © 2004, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Huehn, Jochen Siegmund, Kerstin Lehmann, Joachim C.U. Siewert, Christiane Haubold, Uta Feuerer, Markus Debes, Gudrun F. Lauber, Joerg Frey, Oliver Przybylski, Grzegorz K. Niesner, Uwe de la Rosa, Maurus Schmidt, Christian A. Bräuer, Rolf Buer, Jan Scheffold, Alexander Hamann, Alf Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells |
title | Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells |
title_full | Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells |
title_fullStr | Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells |
title_full_unstemmed | Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells |
title_short | Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells |
title_sort | developmental stage, phenotype, and migration distinguish naive- and effector/memory-like cd4(+) regulatory t cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211798/ https://www.ncbi.nlm.nih.gov/pubmed/14757740 http://dx.doi.org/10.1084/jem.20031562 |
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