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.
Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4+ Regulatory T Cells
J. Huehn and K. Siegmund contributed equally to this work.
The online version of this article includes supplemental material.
Abbreviations used in this paper: DNFB, 2,4-dinitrofluorobenzene; ICOS, inducible costimulator; mBSA, methylated BSA; SA, streptavidin; TREC, T cell receptor excision circle; Treg, regulatory T cell.
Jochen Huehn, Kerstin Siegmund, Joachim C.U. Lehmann, Christiane Siewert, Uta Haubold, Markus Feuerer, Gudrun F. Debes, Joerg Lauber, Oliver Frey, Grzegorz K. Przybylski, Uwe Niesner, Maurus de la Rosa, Christian A. Schmidt, Rolf Bräuer, Jan Buer, Alexander Scheffold, Alf Hamann; Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4+ Regulatory T Cells . J Exp Med 2 February 2004; 199 (3): 303–313. doi: https://doi.org/10.1084/jem.20031562
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