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CXCL9 和 CXCL10 作为类风湿关节炎患者疾病活动的敏感标志物。

CXCL 9 and CXCL 10 as Sensitive markers of disease activity in patients with rheumatoid arthritis.

机构信息

Department of Rheumatology, Hospital Selayang, Selangor, Malaysia.

出版信息

J Rheumatol. 2010 Feb;37(2):257-64. doi: 10.3899/jrheum.090769. Epub 2009 Dec 23.

Abstract

OBJECTIVE

To assess whether serum levels of CC and CXC chemokines correlate with disease activity in patients with rheumatoid arthritis (RA), and to determine whether these effects predict clinical response.

METHODS

Serum levels of the chemokines CC (CCL2, CCL5) and CXC (CXCL8, CXCL9, CXCL10) were quantified at baseline and after 12 weeks of treatment with disease-modifying antirheumatic drugs or biologic agents in 28 patients using flow cytometry. Serum from 40 healthy individuals was collected for comparison at baseline. Response to treatment was classified according to the European League Against Rheumatism (EULAR) response criteria. Remission of disease was defined as a Disease Activity Score < 2.6.

RESULTS

The baseline serum concentrations of CC and CXC chemokines were significantly elevated in patients with active RA compared to healthy controls (p < 0.05) except for CCL2. Significant improvement in all disease activity measurements was observed after 12 weeks of treatment. Seventeen (60.7%) patients achieved good to moderate response based on the EULAR response criteria, and 5 (17.9%) patients achieved remission. The improvement in clinical activity in patients with RA was accompanied by a significant reduction in the serum concentration of CXCL9 and CXCL10 (p < 0.001). A significant reduction in the serum level of CXCL10 was also observed in the group that achieved EULAR response. Serum concentration of CCL5 remained significantly elevated in patients with RA (n = 5) who achieved remission compared to the healthy controls (p < 0.05).

CONCLUSION

Serum concentration of CXCL9 and CXCL10 may serve as sensitive biomarkers for disease activity in patients with RA.

摘要

目的

评估类风湿关节炎(RA)患者血清 CC 和 CXC 趋化因子水平与疾病活动度的相关性,并确定这些效应是否能预测临床反应。

方法

采用流式细胞术检测 28 例患者在接受疾病修饰抗风湿药物或生物制剂治疗 12 周前后及 40 例健康对照者(基线)血清中 CC(CCL2、CCL5)和 CXC(CXCL8、CXCL9、CXCL10)趋化因子的水平。根据欧洲抗风湿病联盟(EULAR)反应标准对治疗反应进行分类。疾病缓解定义为疾病活动评分(DAS)<2.6。

结果

与健康对照组相比,活动期 RA 患者基线时血清 CC 和 CXC 趋化因子浓度显著升高(p<0.05),但 CCL2 除外。治疗 12 周后,所有疾病活动度测量均显著改善。根据 EULAR 反应标准,17 例(60.7%)患者达到良好至中度反应,5 例(17.9%)患者达到缓解。RA 患者临床活动度的改善伴随着血清 CXCL9 和 CXCL10 浓度的显著降低(p<0.001)。在达到 EULAR 反应的患者中,也观察到血清 CXCL10 水平显著降低。与健康对照组相比,达到缓解的 RA 患者(n=5)血清 CCL5 浓度仍显著升高(p<0.05)。

结论

血清 CXCL9 和 CXCL10 浓度可能是 RA 患者疾病活动的敏感生物标志物。

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