Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4+ Regulatory T Cells

Author:

Huehn Jochen1,Siegmund Kerstin1,Lehmann Joachim C.U.1,Siewert Christiane1,Haubold Uta1,Feuerer Markus1,Debes Gudrun F.1,Lauber Joerg2,Frey Oliver3,Przybylski Grzegorz K.45,Niesner Uwe6,de la Rosa Maurus6,Schmidt Christian A.4,Bräuer Rolf3,Buer Jan2,Scheffold Alexander6,Hamann Alf1

Affiliation:

1. Experimentelle Rheumatologie, Medizinische Klinik, Charité, Humboldt-Universitaet, 10117 Berlin, Germany

2. Mukosale Immunitaet, Gesellschaft für Biotechnologische Forschung, 38124 Braunschweig, Germany

3. Institut fuer Pathologie, Universitaet Jena, 07743 Jena, Germany

4. Universitaet Greifswald, 17487 Greifswald, Germany

5. Institute of Human Genetics, Polish Academy of Sciences, 60479 Poznan, Poland

6. Deutsches Rheumaforschungszentrum, 10117 Berlin, Germany

Abstract

Regulatory T cells (Tregs) fulfill a central role in immune regulation. We reported previously that the integrin αEβ7 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. αE−CD25+ cells expressed L-selectin and CCR7, enabling recirculation through lymphoid tissues. In contrast, αE-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, αE-expressing cells were found to be the most potent suppressors of inflammatory processes in disease models such as antigen-induced arthritis.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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