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The role of chemokines in adjusting the balance between CD4+effector T cell subsets and FOXp3-negative regulatory T cells

机译:趋化因子在调节CD4 +效应T细胞亚群和FOXp3阴性调节性T细胞之间的平衡中的作用

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摘要

Chemokines are small (similar to 8-14 kDa) structurally-related chemotactic cytokines that regulate cell trafficking through interactions with specific seven-trans membrane, G protein-coupled receptors (GPCRs). One of the important features of G protein-coupled receptors (GPCRs) is their ability to transmit diverse signaling cascades upon binding different ligands. The current review focuses on the interplay between three ligands: CXCL9, CXCL10 and CXCL11 binding the same receptor (CXCR3) on CD4 + T cells, yet direct different signaling cascades to shape T cell mediated immunity. The review brings about a new concept regarding the biological activities of chemokines in shaping CD4 + T cell immunity, and also a new approach for applying chemokine based therapy of autoimmune diseases. (C) 2015 Elsevier B.V. All rights reserved.
机译:趋化因子是与结构相关的趋化性细胞因子,很小(类似于8-14 kDa),可通过与特定的七跨膜G蛋白偶联受体(GPCR)相互作用来调节细胞运输。 G蛋白偶联受体(GPCR)的重要特征之一是它们能够在结合不同的配体后传递不同的信号级联。当前的评论集中在三种配体之间的相互作用:CXCL9,CXCL10和CXCL11结合CD4 + T细胞上的同一受体(CXCR3),但指导不同的信号级联反应来塑造T细胞介导的免疫力。审查带来了有关趋化因子在塑造CD4 + T细胞免疫方面的生物学活性的新概念,也为基于趋化因子的自身免疫性疾病治疗应用提供了新途径。 (C)2015 Elsevier B.V.保留所有权利。

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