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CCR4 皮肤嗜性表型是健康受试者和银屑病患者中央记忆 CD8 T 细胞的特征。

CCR4 Skin-Tropic Phenotype as a Feature of Central Memory CD8 T Cells in Healthy Subjects and Psoriasis Patients.

机构信息

Department of Morphology, Surgery and Experimental Medicine and LTTA Centre, University of Ferrara, Ferrara, Italy.

IRCCS Istituto Ortopedico Galeazzi, Milan, Italy.

出版信息

Front Immunol. 2020 Apr 3;11:529. doi: 10.3389/fimmu.2020.00529. eCollection 2020.

Abstract

The chemokine receptor CCR4 has emerged as a skin-homing molecule important for the migration of T cells from the blood to the dermis. From our previous data on psoriasis patients, CCR4 memory T cells emerged as a putative recirculating population between skin and blood. Here we focused our attention on the expression of CCR4 and skin-tropic molecules in the different stages of memory T cell differentiation. We analyzed the chemokine receptor profile in CD8 and CD4 CD45RACCR7 (T) and CD45RACCR7 (T) cells. Subpopulations were further divided on the basis of CD62L expression, and the distribution among the subsets of the skin-homing molecule CLA (Cutaneous Lymphocyte Antigen) was evaluated. The characterization was performed on peripheral blood mononuclear cells isolated from 21 healthy subjects and 24 psoriasis patients. The results indicate that (i) the skin-homing CCR4 marker is mainly expressed in T cells, (ii) CCR4 T cells also express high level of CLA and that (iii) the more differentiated phenotype T expresses CXCR3 and CCR5 but lower level of CCR4 and CLA. This indicates that progressive stages of memory T cell differentiation have profoundly different chemokine receptor patterns, with CD8 T displaying a marked skin-tropic phenotype CLACCR4. Differential skin-tropic phenotype between T and T cells was observed in both healthy subjects and psoriasis patients. However, patients showed an expanded circulating population of CD8 T cells with phenotype CCR4CXCR3 that could play a role in the pathophysiology of psoriasis and possibly in disease recurrence.

摘要

趋化因子受体 CCR4 已成为一种皮肤归巢分子,对于 T 细胞从血液迁移到真皮至关重要。根据我们之前在银屑病患者中的数据,CCR4 记忆 T 细胞作为一种在皮肤和血液之间循环的假定群体出现。在这里,我们将注意力集中在记忆 T 细胞分化的不同阶段中 CCR4 和皮肤归巢分子的表达上。我们分析了 CD8 和 CD4 CD45RACCR7(T)和 CD45RACCR7(T)细胞中趋化因子受体的特征。根据 CD62L 的表达进一步划分亚群,并评估皮肤归巢分子 CLA(皮肤淋巴细胞抗原)在亚群中的分布。该特征是在从 21 名健康受试者和 24 名银屑病患者中分离的外周血单核细胞上进行的。结果表明:(i)皮肤归巢 CCR4 标志物主要在 T 细胞中表达;(ii)CCR4 T 细胞也高表达 CLA;(iii)分化程度更高的 T 细胞表达 CXCR3 和 CCR5,但 CCR4 和 CLA 的表达水平较低。这表明记忆 T 细胞分化的渐进阶段具有明显不同的趋化因子受体模式,CD8 T 细胞显示出明显的皮肤归巢表型 CLACCR4。在健康受试者和银屑病患者中均观察到 T 和 T 细胞之间的不同皮肤归巢表型。然而,患者显示出具有表型 CCR4CXCR3 的循环 CD8 T 细胞的扩增,这可能在银屑病的发病机制中发挥作用,并且可能在疾病复发中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/347a/7147166/d0ffe83ee1fe/fimmu-11-00529-g0001.jpg

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