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 alphaEbeta7 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. alphaE-CD25+ c...

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Veröffentlicht in:The Journal of experimental medicine 2004-02, Vol.199 (3), p.303-313
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung:Regulatory T cells (Tregs) fulfill a central role in immune regulation. We reported previously that the integrin alphaEbeta7 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. alphaE-CD25+ cells expressed L-selectin and CCR7, enabling recirculation through lymphoid tissues. In contrast, alphaE -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, alphaE -expressing cells were found to be the most potent suppressors of inflammatory processes in disease models such as antigen-induced arthritis.
ISSN:0022-1007
1540-9538
DOI:10.1084/jem.20031562