Department of Clinical Immunology, State Key Discipline of Cell Biology, First Affiliated Hospital, Fourth Military Medical University, No. 127 West Changle Road, Xi'an, 710032, Shaanxi Province, People's Republic of China.
J Clin Immunol. 2013 Jan;33(1):151-61. doi: 10.1007/s10875-012-9774-0. Epub 2012 Aug 29.
To investigate the effects of TNF-α blockage on levels of circulating Th17, Treg and their related cytokines in ankylosing spondylitis (AS) patients with different response to anti-TNF-α therapy.
The frequencies of circulating Th17 and Treg and serum levels of related cytokines were determined using flow cytometry analysis and ELISA, respectively, in 222 AS patients both before (baseline) and 6 months after anti-TNF-α therapy. Therapeutic response was defined according to ASAS (Assessment in Spondyloarthritis International Society) response criteria.
Significantly higher baseline circulating Th17 and serum TNF-α, IL-6, IL-17, IL-23 were observed in active AS patients than in healthy controls. After anti-TNF-α therapy, 168 patients (75.7 %) were responders and 54 (24.3 %) were non-responders. Frequencies of Th17 significantly decreased in responders, but significantly increased in non-responders. Treg increased significantly in responders but decreased significantly in non-responders. Levels of TNF-α, IL-6, IL-17, and IL-23 were significantly decreased in responders. In contrast, IL-17 and IL-23 significantly increased in non-responders. TGF-β were significantly increased only in responders, whereas no significant changes were seen in IL-10 in either responders or non-responders. Spearman correlation analysis showed that frequencies of Th17 and levels of TNF-α, IL-6, IL-17, and IL-23 were positively correlated with BASDAI score. They were also positively correlated with BASFI score except for IL-6. Treg were found to be negatively correlated with BASDAI score.
The beneficial effect of anti-TNF-α therapy in AS might not only neutralize the effects of TNF-α but also down-regulate Th17 and Th17-related cytokines accompanied by up-regulating the Treg/TGF-β axis in responders.
探讨肿瘤坏死因子-α(TNF-α)阻断对不同抗 TNF-α 治疗反应的强直性脊柱炎(AS)患者循环 Th17、Treg 及其相关细胞因子水平的影响。
采用流式细胞术分析和酶联免疫吸附试验(ELISA)分别检测 222 例 AS 患者抗 TNF-α 治疗前后(基线)循环 Th17 和 Treg 及相关细胞因子的血清水平。根据 ASAS(国际脊柱关节炎评估协会)反应标准定义治疗反应。
活动期 AS 患者的循环 Th17 和血清 TNF-α、IL-6、IL-17、IL-23 水平明显高于健康对照组。抗 TNF-α 治疗后,168 例(75.7%)患者为应答者,54 例(24.3%)为无应答者。应答者 Th17 频率显著降低,而无应答者显著升高。应答者 Treg 显著增加,而无应答者显著减少。应答者 TNF-α、IL-6、IL-17 和 IL-23 水平显著降低。相反,无应答者的 IL-17 和 IL-23 水平显著升高。仅在应答者中 TGF-β 显著增加,而在应答者或无应答者中 IL-10 均未见明显变化。Spearman 相关分析表明,Th17 频率和 TNF-α、IL-6、IL-17 和 IL-23 水平与 BASDAI 评分呈正相关。它们与 BASFI 评分呈正相关,除了 IL-6。Treg 与 BASDAI 评分呈负相关。
抗 TNF-α 治疗 AS 的有益效果不仅可能中和 TNF-α 的作用,而且可能下调 Th17 和 Th17 相关细胞因子,同时在应答者中上调 Treg/TGF-β 轴。