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Effects of interferon β-1a and interferon β-1b monotherapies on selected serum cytokines and nitrite levels in patients with relapsing-remitting multiple sclerosis: A 3-year longitudinal study

机译:干扰素β-1a和干扰素β-1b单一疗法对复发缓解型多发性硬化症患者血清细胞因子和亚硝酸盐水平的影响:一项为期三年的纵向研究

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Objective: Interferon (IFN)β treatment is a mainstay of relapsing-remitting multiple sclerosis (RRMS) immunotherapy. Its efficacy is supposedly a consequence of impaired trafficking of inflammatory cells into the central nervous system and modification of the proinflammatory/antiinflammatory cytokine balance. However, the effects of long-term monotherapy using various IFNβ preparations on cytokine profiles and the relevance of these effects for the therapy outcome have not yet been elucidated. Methods: Changes were compared in serum levels of TNFα, IFNγ, interleukin (IL)-6, IL-10 and nitrite between RRMS patients given 3-year treatment with intramuscular IFNβ-1a (30 μg once a week) or subcutaneous IFNβ-1b (250 μg every other day). Only the data from patients who completed the 3-year study (n = 20 and n = 18, respectively) were analyzed. Results: Three-year IFNβ-1a or IFNβ-1b monotherapy reduced serum nitrite levels by 77 and 71%, respectively, lowered multiple sclerosis relapse annual rate by 70 and 71%, respectively, and significantly and similarly lowered Expanded Disability Status Scale scores in both study groups (by 0.9 on average). The two monotherapies showed little if any effect on cytokine levels and cytokine level ratios after the first year, but exerted diverging effects on these indices later on; the only exception was the IFNγ/IL-6 ratio that showed a monotonous rise in both study groups over the entire study period. Conclusion: During long-term IFNβ monotherapy, the levels of the studied cytokines show no relevance to the course of RRMS and neurological status of patients, whereas there seems to be a link between these clinical indices and the activity of nitric oxide-mediated pathways.
机译:目的:干扰素(IFN)β治疗是复发-缓解型多发性硬化症(RRMS)免疫疗法的主要手段。据认为其功效是炎症细胞向中枢神经系统运输受损和促炎/抗炎细胞因子平衡改变的结果。然而,尚未阐明使用各种IFNβ制剂的长期单一疗法对细胞因子谱的影响以及这些效应与治疗结果的相关性。方法:比较接受肌肉内IFNβ-1a(每周一次30μg)或皮下IFNβ-1b治疗3年的RRMS患者的血清TNFα,IFNγ,白介素(IL)-6,IL-10和亚硝酸盐水平的变化。 (隔天250μg)。仅分析了完成3年研究的患者(分别为n = 20和n = 18)的数据。结果:三年的IFNβ-1a或IFNβ-1b单药治疗分别使血清亚硝酸盐水平降低了77%和71%,使多发性硬化症的年复发率分别降低了70%和71%,并且显着且类似地降低了扩展的残疾状态量表评分两个研究组(平均0.9)。在第一年后,这两种单一疗法对细胞因子水平和细胞因子水平比率几乎没有影响,但后来对这些指标产生了分歧。唯一的例外是IFNγ/ IL-6比例在整个研究期内均显示两个研究组均单调上升。结论:在长期的IFNβ单药治疗期间,所研究的细胞因子水平与RRMS的病程和患者的神经系统状况无关,而这些临床指标与一氧化氮介导的通路活性之间似乎存在联系。

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