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干扰素β-1a注射时间和治疗持续时间会影响多发性硬化症患者的临床副作用以及血浆激素和细胞因子水平的急性变化。

Time of interferon-beta 1a injection and duration of treatment affect clinical side effects and acute changes of plasma hormone and cytokine levels in multiple sclerosis patients.

作者信息

Kümpfel T, Schwan M, Pollmächer Th, Yassouridis A, Uhr M, Trenkwalder C, Weber F

机构信息

Institute of Clinical Neuroimmunology, Klinikum Grosshadern, Ludwig-Maximilians-Universität, Munich, Germany.

出版信息

Mult Scler. 2007 Nov;13(9):1138-45. doi: 10.1177/1352458507078685.

Abstract

During initiation of interferon-beta (IFN-beta) therapy, many multiple sclerosis (MS) patients experience systemic side effects which may depend on the time point of IFN-beta injection. We investigated the time course of plasma hormone-, cytokine- and cytokine-receptor concentrations after the first injection of IFN-beta either at 8.00 a.m. (group A) or at 6.00 p.m. (group B) and quantified clinical side effects within the first 9 h in 16 medication free patients with relapsing-remitting MS. This investigation was repeated after 6-month IFN-beta therapy. Plasma ACTH and cortisol concentrations followed their physiological rhythms, with lower levels in the evening compared to the morning, but raised earlier and stronger in group B after IFN-beta administration. IFN-beta injection in the evening led to a prompter increase of plasma IL-6 concentrations and temperature during the first hours and correlated to more intense clinical side effects compared to group A. Plasma IL-10 concentrations increased more in group A compared to group B, but sTNF-RI and sTNF-RII concentrations raised 7 h after IFN-beta injection only in group B. Acute effects on plasma hormone and cytokine concentrations adapted after 6-month IFN-beta treatment, while diurnal variations were still present. Baseline sTNF-RII concentrations were elevated after 6-month IFN-beta therapy only in group A. Our results show that time point of IFN-beta injection has differential effects on acute changes of plasma hormone and cytokine concentrations and is related to systemic side effects. This may have implications on the tolerability and effectiveness of IFN-beta therapy.

摘要

在干扰素-β(IFN-β)治疗开始期间,许多多发性硬化症(MS)患者会出现全身性副作用,这些副作用可能取决于IFN-β注射的时间点。我们调查了16例未经治疗的复发缓解型MS患者在上午8点(A组)或下午6点(B组)首次注射IFN-β后血浆激素、细胞因子和细胞因子受体浓度的时间变化过程,并在最初9小时内对临床副作用进行了量化。在IFN-β治疗6个月后重复此项研究。血浆促肾上腺皮质激素(ACTH)和皮质醇浓度遵循其生理节律,与上午相比,晚上水平较低,但在IFN-β给药后,B组升高得更早且更强烈。晚上注射IFN-β会导致最初几个小时内血浆白细胞介素-6(IL-6)浓度和体温更快升高,与A组相比,临床副作用更强烈。与B组相比,A组血浆白细胞介素-10(IL-10)浓度升高更多,但可溶性肿瘤坏死因子受体I(sTNF-RI)和可溶性肿瘤坏死因子受体II(sTNF-RII)浓度仅在B组IFN-β注射后7小时升高。IFN-β治疗6个月后,对血浆激素和细胞因子浓度的急性影响有所适应,但昼夜变化仍然存在。仅在A组中,IFN-β治疗6个月后基线sTNF-RII浓度升高。我们的结果表明,IFN-β注射时间点对血浆激素和细胞因子浓度的急性变化有不同影响,并与全身性副作用相关。这可能对IFN-β治疗的耐受性和有效性有影响。

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