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淋巴细胞趋化因子CCL21共刺激初始T细胞扩增以及非调节性CD4+ T细胞的Th1极化。

The lymphoid chemokine CCL21 costimulates naive T cell expansion and Th1 polarization of non-regulatory CD4+ T cells.

作者信息

Flanagan Kenneth, Moroziewicz Dorota, Kwak Heesun, Hörig Heidi, Kaufman Howard L

机构信息

Department of Pathology, Columbia University, New York, NY 10032, USA.

出版信息

Cell Immunol. 2004 Sep-Oct;231(1-2):75-84. doi: 10.1016/j.cellimm.2004.12.006. Epub 2005 Jan 21.

Abstract

CCL21 (SLC/6Ckine) is constitutively expressed by secondary lymphoid tissue and attracts CCR7-expressing mature dendritic cells and naive T cells. Recent studies demonstrated that intra-tumoral delivery of CCL21 induces tumor regression in a T cell dependent manner. CCL21 is known to mediate T cell trafficking but little is known about its function as a costimulatory molecule. Herein, we demonstrate that CCL21 costimulates expansion of CD4+ and CD8+ T cells and induces Th1 polarization. These effects were specific for naive T cells, and we show that CD4+CD25+ regulatory T cells were hyporesponsive to CCL21 induced migration, and unresponsive to CCL21 costimulation. These unique functions of CCL21 to both attract naive T cells as well as costimulate their proliferation and differentiation, suggests that CCL21 is a pivotal molecule for priming T cell responses and has therapeutic implications for local delivery of CCL21. The coordinated effects of CCL21 on T cell migration and activation may also represent a more comprehensive paradigm for the activity of other chemokines as well.

摘要

CCL21(SLC/6Ckine)由二级淋巴组织组成性表达,可吸引表达CCR7的成熟树突状细胞和初始T细胞。最近的研究表明,肿瘤内递送CCL21以T细胞依赖的方式诱导肿瘤消退。已知CCL21介导T细胞转运,但对其作为共刺激分子的功能了解甚少。在此,我们证明CCL21共刺激CD4+和CD8+T细胞的扩增并诱导Th1极化。这些效应是初始T细胞特有的,并且我们表明CD4+CD25+调节性T细胞对CCL21诱导的迁移反应低下,对CCL21共刺激无反应。CCL21吸引初始T细胞以及共刺激其增殖和分化的这些独特功能表明,CCL21是引发T细胞反应的关键分子,并且对CCL21的局部递送具有治疗意义。CCL21对T细胞迁移和激活的协同作用也可能代表了其他趋化因子活性的更全面模式。

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