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

机译:发育阶段,表型和迁移区分幼稚和效应/记忆样CD4 +调节性T细胞

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摘要

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.
机译:调节性T细胞(Tregs)在免疫调节中起着核心作用。我们之前曾报道过,整合素αEβ7可以区分鼠CD4 +调节性T细胞的不同亚群。现在,使用该标记有助于阐明调节性T细胞之间的基本二分法。 αE-CD25+细胞表达L-选择蛋白和CCR7,从而可通过淋巴组织再循环。相反,αE阳性亚群(CD25 +和CD25-)表现出一种效应子/记忆表型,表达高水平的E / P-选择蛋白结合配体,多种粘附分子以及炎性趋化因子的受体,从而可有效迁移至发炎部位。因此,发现在疾病模型例如抗原诱导的关节炎中,表达αE的细胞是炎症过程最有效的抑制剂。

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