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Evaluation of Anti-inflammatory Effects of Steroids and Arthritis-Related Biotherapies in an In Vitro Coculture Model with Immune Cells and Synoviocytes

机译:在免疫细胞和滑膜细胞的体外共培养模型中评估类固醇和关节炎相关生物疗法的抗炎作用

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Background During rheumatoid arthritis (RA), steroids and biotherapies are used alone and combined. Efficacy has been established in clinical trials but their differential effects at the cellular level are less documented. The aim was to study these cellular effects using an in vitro model with synoviocytes interacting with peripheral blood mononuclear cells (PBMC) to reproduce the interactions in the RA synovium. Methods Activated-PBMC were cocultured with RA synoviocytes during 48?h. A dose–response of methylprednisolone (MP) was tested and different biotherapies (Infliximab, Etanercept, Adalimumab, Tocilizumab, Abatacept, and Rituximab) were added alone or in combination with MP. Cytokine production (IL-17, IL-6, IL-1β, IFN-γ and IL-10) was measured by ELISA. Results Addition of MP to cocultures inhibited the production of all cytokines. The response to the biotherapies alone was treatment-dependent. IL-17 production was inhibited only by Tocilizumab ( p ?=?0.004), while IL-6 was decreased only by Infliximab ( p ?≤?0.002). IL-1β level was affected in all conditions ( p ?≤?0.03). IFN-γ production was mainly decreased by Infliximab ( p ?=?0.004) and IL-10 by Infliximab and Tocilizumab ( p ?≤?0.004). The combination MP and biotherapies did not induce an additional effect on pro-inflammatory cytokine inhibition. The combination MP and biotherapies induced a higher IL-10 secretion than MP alone, mainly with Rituximab. Conclusion Steroids inhibited the secretion of all cytokines, and low doses were as potent. The anti-inflammatory effect of biotherapies was dependent on their mechanism of action. MP and biotherapy combination did not enhance the inhibitory effect on pro-inflammatory cytokines but could have a beneficial effect by increasing IL-10 production.
机译:背景在类风湿关节炎(RA)期间,类固醇和生物疗法可单独使用或组合使用。功效已经在临床试验中确立,但它们在细胞水平上的差异作用尚无文献记载。目的是使用滑膜细胞与外周血单核细胞(PBMC)相互作用以在RA滑膜中复制相互作用的体外模型研究这些细胞效应。方法活化的PBMC与RA滑膜细胞共培养48小时。测试了甲基强的松龙(MP)的剂量反应,并单独或与MP组合使用了不同的生物疗法(英夫利昔单抗,依那西普,阿达木单抗,托珠单抗,阿巴西普和利妥昔单抗)。通过ELISA测量细胞因子产生(IL-17,IL-6,IL-1β,IFN-γ和IL-10)。结果在共培养物中添加MP可抑制所有细胞因子的产生。单独对生物疗法的反应取决于治疗。 IL-17的产生仅被Tocilizumab抑制(p = 0.004),而IL-6仅被英夫利昔单抗降低(p≤0.002)。 IL-1β水平在所有条件下均受到影响(p≤≤0.03)。英夫利昔单抗主要降低IFN-γ的表达(p = 0.004),英夫利昔单抗和托珠单抗降低IL-10的表达(p≤0.004)。 MP和生物疗法的结合并未对促炎细胞因子的抑制作用产生额外的影响。 MP和生物疗法的组合诱导的IL-10分泌比单独使用MP(主要是利妥昔单抗)更高。结论类固醇可抑制所有细胞因子的分泌,低剂量有效。生物疗法的抗炎作用取决于它们的作用机理。 MP和生物疗法的组合不能增强对促炎细胞因子的抑制作用,但可以通过增加IL-10产生而产生有益的作用。

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