Developmental stage, phenotype, and migration distinguish naive- and effector/memory-like CD4+ regulatory T cells

被引:512
作者
Huehn, J
Siegmund, K
Lehmann, JCU
Siewert, C
Haubold, U
Feuerer, M
Debes, GF
Lauber, J
Frey, O
Przybylski, GK
Niesner, U
de la Rosa, M
Schmidt, CA
Bäuer, R
Buer, J
Scheffold, A
Hamann, A
机构
[1] Humboldt Univ, DRFZ, Med Klin, Charite, D-10117 Berlin, Germany
[2] Gesell Biotechnol Forsch mbH, Mukosale Immunitaet, D-38124 Braunschweig, Germany
[3] Univ Jena, Inst Pathol, D-07743 Jena, Germany
[4] Ernst Moritz Arndt Univ Greifswald, D-17487 Greifswald, Germany
[5] Polish Acad Sci, Inst Human Genet, PL-60479 Poznan, Poland
[6] Deutsch Rheumaforschungszentrum, D-10117 Berlin, Germany
关键词
CD103; CD25; lymphocyte migration; chemokines; inflammation;
D O I
10.1084/jem.20031562
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells (Tregs) fulfill a central role in immune regulation. We reported previously that the integrin alpha(E)beta(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. alpha(E)(-)CD25(+) cells expressed L-selectin and CCR7, enabling recirculation through lymphoid tissues. In contrast, alpha(E)-positve 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, alpha(E)-expressing cells were found to be the most potent suppressors of inflammatory processes in disease models such as antigen-induced arthritis.
引用
收藏
页码:303 / 313
页数:11
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