类风湿性关节炎中的促炎细胞因子:与 Janus 激酶和白细胞介素 6 抑制剂疗法相抗衡的动态变化

A. A. Baranov, N. Lapkina, E. A. Leontyeva, A. Karateev, A. A. Kolinyko, A. P. Pavluchkov, A. Artyuhov, I. A. Gorohov
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The study included 30 patients with a reliable diagnosis of RA, advanced stage of disease, with moderate or high RA activity and ineffectiveness of previous therapy with csDMARD or bDMARD for at least 6 months. 10 patients received TOFA at a dose of 5 mg twice daily 10 received UPA at a dose of 15 mg once daily and 10 were on OKZ therapy at a dose of 64 mg subcutaneously every 4 weeks. Studies were performed before treatment, after 3 and 6 months of therapy. The levels of IL-1β, IL-6, IL-17A, IL-17F, IL-23, IL-31, IL-33, INF-γ, TNF-α in serum were investigated using multiplex xMAR technology on Bio-PlexTM 200 System analyser (BIO-RAD, USA).Results. In all groups of patients after 3 and 6 months from the start of therapy, there was a significant decrease in the RA activity index compared to baseline values. The concentration of IL-1β, IL-17A, IL-17F and IL-23 did not change significantly during treatment with any of the drugs. IL-6 values on TOFA background significantly decreased after 3 and 6 months of follow-up compared to the baseline level. UPA therapy had no effect on IL-6 level during the whole observation period, and against the background of OKZ application its values significantly increased after 3 months, and after 6 months – decreased, remaining higher than the initial values. The concentration of IL-31 after 3 months of TOFA treatment significantly decreased (respectively: 6.95 (3.85; 17.72) pg/ml and 3.00 (1.50; 3.85) pg/ml, p<0.05), and after 6 months – increased, but remained lower than baseline (5.09 (3.85; 6.33) pg/ml, p<0.05). IL-33 level on the background of UPA decreased and after 6 months was significantly lower than baseline (1.11 (0.86; 3.95) pg/ ml; 1.05 (0.37; 3.95) and 0.37 (0.12; 1.23) pg/ml, p<0.05). 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The study included 30 patients with a reliable diagnosis of RA, advanced stage of disease, with moderate or high RA activity and ineffectiveness of previous therapy with csDMARD or bDMARD for at least 6 months. 10 patients received TOFA at a dose of 5 mg twice daily 10 received UPA at a dose of 15 mg once daily and 10 were on OKZ therapy at a dose of 64 mg subcutaneously every 4 weeks. Studies were performed before treatment, after 3 and 6 months of therapy. The levels of IL-1β, IL-6, IL-17A, IL-17F, IL-23, IL-31, IL-33, INF-γ, TNF-α in serum were investigated using multiplex xMAR technology on Bio-PlexTM 200 System analyser (BIO-RAD, USA).Results. In all groups of patients after 3 and 6 months from the start of therapy, there was a significant decrease in the RA activity index compared to baseline values. The concentration of IL-1β, IL-17A, IL-17F and IL-23 did not change significantly during treatment with any of the drugs. 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引用次数: 0

摘要

血清和滑膜液中促炎细胞因子的分泌增加在RA的发病机制中起着重要作用。JAK 抑制剂和 bDMARD 旨在抑制由其引起的各种病理反应。在实际临床实践中确定 JAK 和 IL-6 抑制剂治疗对 RA 患者促炎细胞因子浓度的影响。研究纳入了 30 名确诊为 RA、疾病晚期、具有中度或高度 RA 活动性、既往使用 csDMARD 或 bDMARD 治疗至少 6 个月无效的患者。其中 10 名患者接受 TOFA 治疗,剂量为 5 毫克,每天两次;10 名患者接受 UPA 治疗,剂量为 15 毫克,每天一次;10 名患者接受 OKZ 治疗,剂量为 64 毫克,每 4 周皮下注射一次。研究分别在治疗前、治疗 3 个月和 6 个月后进行。在 Bio-PlexTM 200 系统分析仪(美国 BIO-RAD)上使用多重 xMAR 技术检测了血清中 IL-1β、IL-6、IL-17A、IL-17F、IL-23、IL-31、IL-33、INF-γ、TNF-α 的水平。自治疗开始 3 个月和 6 个月后,各组患者的 RA 活动指数与基线值相比均显著下降。在使用任何一种药物治疗期间,IL-1β、IL-17A、IL-17F 和 IL-23 的浓度均无明显变化。与基线水平相比,TOFA背景下的IL-6值在随访3个月和6个月后明显下降。在整个观察期间,UPA疗法对IL-6水平没有影响,而在应用OKZ的背景下,IL-6的数值在3个月后明显升高,6个月后有所下降,但仍高于初始值。经过 3 个月的 TOFA 治疗后,IL-31 的浓度明显下降(分别为 6.95(3.85;6.85;6.95;6.85;6.85):6.95 (3.85; 17.72) pg/ml 和 3.00 (1.50; 3.85) pg/ml,p<0.05),6 个月后有所上升,但仍低于基线值(5.09 (3.85; 6.33) pg/ml,p<0.05)。在 UPA 的背景下,IL-33 水平下降,6 个月后明显低于基线(1.11 (0.86; 3.95) pg/ml; 1.05 (0.37; 3.95) and 0.37 (0.12; 1.23) pg/ml,p<0.05)。与开始治疗时相比,服用 TOFA 3 个月和 6 个月后 INF-γ 的浓度明显下降(2.05 (1.48; 3.19) pg/ml; 0.99 (0.49; 2.05) pg/ml 和 0.99 (0.49; 2.62) pg/ml,p<0.05)。与基线值相比,OKZ治疗6个月后TNF-α水平升高,分别为0.79 (0.41; 0.98) pg/ml和1.23 (0.67; 2.06) pg/ml,p<0.05。对RA患者使用TOFA、UPA和OKZ对疾病活动有积极影响,但对血清中的促炎细胞因子水平有不同影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proinflammatory cytokines in rheumatoid arthritis: dynamics against therapy with Janus kinase and interleukin 6 inhibitors
Increased production of proinflammatory cytokines in serum and synovial fluid plays an important role in the pathogenesis of RA. JAK inhibitors and bDMARD are aimed at suppressing various pathological reactions caused by them.The aim of the study. To determine the effect of therapy with JAK and IL-6 inhibitors on the concentration of proinflammatory cytokines in RA patients in real clinical practice.Materials and methods. The study included 30 patients with a reliable diagnosis of RA, advanced stage of disease, with moderate or high RA activity and ineffectiveness of previous therapy with csDMARD or bDMARD for at least 6 months. 10 patients received TOFA at a dose of 5 mg twice daily 10 received UPA at a dose of 15 mg once daily and 10 were on OKZ therapy at a dose of 64 mg subcutaneously every 4 weeks. Studies were performed before treatment, after 3 and 6 months of therapy. The levels of IL-1β, IL-6, IL-17A, IL-17F, IL-23, IL-31, IL-33, INF-γ, TNF-α in serum were investigated using multiplex xMAR technology on Bio-PlexTM 200 System analyser (BIO-RAD, USA).Results. In all groups of patients after 3 and 6 months from the start of therapy, there was a significant decrease in the RA activity index compared to baseline values. The concentration of IL-1β, IL-17A, IL-17F and IL-23 did not change significantly during treatment with any of the drugs. IL-6 values on TOFA background significantly decreased after 3 and 6 months of follow-up compared to the baseline level. UPA therapy had no effect on IL-6 level during the whole observation period, and against the background of OKZ application its values significantly increased after 3 months, and after 6 months – decreased, remaining higher than the initial values. The concentration of IL-31 after 3 months of TOFA treatment significantly decreased (respectively: 6.95 (3.85; 17.72) pg/ml and 3.00 (1.50; 3.85) pg/ml, p<0.05), and after 6 months – increased, but remained lower than baseline (5.09 (3.85; 6.33) pg/ml, p<0.05). IL-33 level on the background of UPA decreased and after 6 months was significantly lower than baseline (1.11 (0.86; 3.95) pg/ ml; 1.05 (0.37; 3.95) and 0.37 (0.12; 1.23) pg/ml, p<0.05). The concentration of INF-γ after 3 and 6 months of TOFA administration decreased significantly compared to the start of therapy (2.05 (1.48; 3.19) pg/ml; 0.99 (0.49; 2.05) pg/ml and 0.99 (0.49; 2.62) pg/ml, p<0.05). Treatment with OKZ resulted in increased TNF-α levels after 6 months compared to baseline values of 0.79 (0.41; 0.98) pg/ml and 1.23 (0.67; 2.06) pg/ml, p<0.05.Conclusions. The use of TOFA, UPA and OKZ in RA patients has a positive effect on disease activity, but has different effects on the level of proinflammatory cytokines in serum.
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