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多发性肌炎和皮肌炎患者外周血淋巴细胞中趋化因子受体表达的改变。

Altered chemokine receptor expression in the peripheral blood lymphocytes in polymyositis and dermatomyositis.

机构信息

Department of Rheumatology and Immunology, First Affiliated Hospital, China Medical University, Shenyang 110001, People's Republic of China.

Department of 1st Cancer Institute, First Affiliated Hospital, China Medical University, Shenyang 110001, People's Republic of China.

出版信息

Cytokine. 2017 Nov;99:316-321. doi: 10.1016/j.cyto.2017.08.018. Epub 2017 Aug 30.

Abstract

OBJECTIVE

To examine the expression of chemokine receptors in different peripheral blood T-cell subsets in patients with polymyositis (PM) and dermatomyositis (DM).

METHODS

We used flow cytometry to measure the frequencies of chemokinereceptors CXCR3 and CCR4 expression in the CD4 or CD8 lymphocytes. Enzyme linked immunosorbent assays were also used to measure the concentrations of C-X-C motif chemokine 10 (CXCL10), thymus and activation regulated chemokine (TARC) and macrophage derived chemokine (MDC).

RESULTS

Comparing to 20 healthy controls, %CD4CXCR3 and %CD8CXCR3 T cells significantly decreased in 33DM patients, and %CD8CXCR3 cells decreased in 24PM patients, but %CD4CCR4 and %CD8CCR4 cells did not significantly change in both the PM and DM patients. Accordingly, the Th1/Th2 polarization, analyzed as the balance obtained after dividing %CD4CXCR3 cells by %CD4CCR4 cells, showed a significant reduction in DM. The serum concentration of CXCR3 ligand, CXCL10, significantly increased and negatively correlated with circulating %CD4CXCR3 cells in DM patients. There was no significant change of TARC and MDC in PM and DM patients. Furthermore, %CD4CXCR3 cells decreased more severely in the patients with interstitial lung disease.

CONCLUSIONS

The present results indicate that the distributions of circulating CXCR3 T-cells differ among the PM and DM cases. Our findings suggest a pathogenic difference between PM and DM.

摘要

目的

研究多发性肌炎(PM)和皮肌炎(DM)患者外周血 T 细胞亚群中趋化因子受体的表达。

方法

我们使用流式细胞术测量 CD4 或 CD8 淋巴细胞中趋化因子受体 CXCR3 和 CCR4 的表达频率。还使用酶联免疫吸附测定法测量 C-X-C 基序趋化因子 10(CXCL10)、胸腺激活调节趋化因子(TARC)和巨噬细胞来源趋化因子(MDC)的浓度。

结果

与 20 名健康对照相比,33 名 DM 患者的 %CD4CXCR3 和 %CD8CXCR3 T 细胞显著减少,24 名 PM 患者的 %CD8CXCR3 细胞减少,但 PM 和 DM 患者的 %CD4CCR4 和 %CD8CCR4 细胞均无明显变化。相应地,Th1/Th2 极化,分析为 %CD4CXCR3 细胞除以 %CD4CCR4 细胞后获得的平衡,在 DM 中显著降低。DM 患者血清 CXCR3 配体 CXCL10 浓度显著升高,与循环 %CD4CXCR3 细胞呈负相关。PM 和 DM 患者的 TARC 和 MDC 没有明显变化。此外,间质性肺病患者的 %CD4CXCR3 细胞减少更为严重。

结论

本研究结果表明,PM 和 DM 患者循环 CXCR3 T 细胞的分布不同。我们的发现表明 PM 和 DM 之间存在致病性差异。

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