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靶向早期类风湿关节炎的 IL-6 信号转导会导致 Th1 和 Th17 抑制以及 Th2 扩张。

Targeting IL-6 signalling in early rheumatoid arthritis is followed by Th1 and Th17 suppression and Th2 expansion.

机构信息

Dipartimento Biomedico di Medicina Interna e Specialistica, Sezione di Reumatologia, Università degli studi di Palermo, Italy.

出版信息

Clin Exp Rheumatol. 2014 Jan-Feb;32(1):77-81. Epub 2014 Jan 14.

Abstract

OBJECTIVES

To investigate the in vitro and ex-vivo effect of IL-6 inhibition on the balance between Th1, Th2, Th17 and Treg cells.

METHODS

Ten consecutive adult patients with active early rheumatoid arthritis (ERA) and ten healthy volunteers were included in the study. The percentages of Th1, Th2, Th17 and Treg cells were analysed by flow cytometry in the peripheral blood mononuclear cells obtained from controls and from RA patients at the time of first evaluation and just before the third TCZ infusion. The in vitro effect of TCZ on the different subsets of CD4+ T cells and the expression levels of Th1, Th2, Th17 and Treg-related cytokines was also assessed.

RESULTS

Treatment with TCZ, both ex vivo and in vitro, resulted in a significant reduction of the percentage of Th1, Th17 and Treg cells with a concomitant significant increase of Th2 cell subsets. The reduction of the different subsets of T lymphocytes was associated with an intense staining with Annexin V, suggesting an apoptotic-related cell reduction. A significant decrease of Th1, Th17 and Treg cytokines and a concomitant increase of IL-4 was also observed after TCZ treatment in PBMC isolated from RA patients.

CONCLUSIONS

TCZ could modify the immune imbalance in RA inducing apoptosis of Th1, Th17 and Treg cells and promoting the appearance of a Th2 response.

摘要

目的

研究白细胞介素 6(IL-6)抑制对 Th1、Th2、Th17 和 Treg 细胞平衡的体外和体内效应。

方法

本研究纳入了 10 例连续的活动期早期类风湿关节炎(ERA)成年患者和 10 例健康志愿者。通过流式细胞术分析来自对照组和 RA 患者首次评估时及第三次 TCZ 输注前外周血单个核细胞中 Th1、Th2、Th17 和 Treg 细胞的百分比。还评估了 TCZ 对 CD4+T 细胞不同亚群的体外作用以及 Th1、Th2、Th17 和 Treg 相关细胞因子的表达水平。

结果

TCZ 的治疗,无论是体外还是体内,均导致 Th1、Th17 和 Treg 细胞的百分比显著降低,同时 Th2 细胞亚群显著增加。不同 T 淋巴细胞亚群的减少与 Annexin V 的强烈染色相关,提示与细胞凋亡相关的减少。在从 RA 患者分离的 PBMC 中,TCZ 治疗后还观察到 Th1、Th17 和 Treg 细胞因子的显著减少和 IL-4 的同时增加。

结论

TCZ 可通过诱导 Th1、Th17 和 Treg 细胞凋亡和促进 Th2 反应来调节 RA 中的免疫失衡。

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