首页> 外文期刊>Journal of neuroinflammation >Intravenous immunoglobulin treatment of the post-polio syndrome: sustained effects on quality of life variables and cytokine expression after one year follow up
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Intravenous immunoglobulin treatment of the post-polio syndrome: sustained effects on quality of life variables and cytokine expression after one year follow up

机译:静脉注射免疫球蛋白治疗脊髓灰质炎后综合症:随访一年后对生活质量和细胞因子表达的持续影响

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Background Expression of inflammatory cytokines in cerebrospinal fluid (CSF) has led to the hypothesis of intrathecal chronic inflammation to explain the denervation observed in post-polio syndrome (PPS). It has been shown that therapy with intravenous immunoglobulin (IVIG) improves physical performance and dampens down the inflammatory process at 6?months in PPS patients. We here examined the effects of IVIG on cytokine expression and clinical outcome one year after IVIG treatment. Methods From a previous study with 135 PPS patients included, 41 patients were further evaluated before un-blinding for one year (21 placebo and 20 treated with IVIG, Xepol? 50?mg/ml), and were assessed for clinical variables by performing the Short Form-36 survey (SF-36) questionnaire assessment, the 6 minute walk distance test (6MWT) and registering pain level by Visual Analogue Scale (VAS) after IVIG treatment. A separate cohort of 37 PPS patients went through lumbar puncture (LP) at baseline and 20 patients, treated with IVIG, repeated the LP one year later. Thirty patients affected with other neurological diseases (OND) were used as control group. Inflammatory cytokines TNF, TGFβ, IFNγ, IL-23, IL-13 and IL-10 were measured in blood cells and CSF cells with RT-PCR. Results Scores of the physical components of SF-36 were significantly higher at the one year follow up time-point in the IVIG-treated patients when compared to baseline as well as to the control subjects. Pain VAS score and 6MWT improved significantly in the IVIG-treated patients when compared with baseline Relative expression of TNF and IFN-γ in both PBMCs and CSF from PPS patients were increased compared to OND subjects at baseline (p?
机译:背景脑脊液(CSF)中炎性细胞因子的表达已导致鞘内慢性炎症的假说,以解释在脊髓灰质炎后综合征(PPS)中观察到的神经支配。研究表明,静脉注射免疫球蛋白(IVIG)可以改善PPS患者6个月时的身体机能并减轻其炎症过程。我们在这里检查了IVIG对IVIG治疗一年后细胞因子表达和临床结局的影响。方法在一项包括135名PPS患者的先前研究中,对41例患者进行了一年的失盲进一步评估(21例安慰剂和20例用IVIG,Xepol?50μmg/ ml治疗),并通过进行盲评估。 IVIG治疗后,进行简短的36型问卷调查(SF-36)问卷评估,6分钟步行距离测试(6MWT)并通过视觉模拟量表(VAS)记录疼痛程度。另一组37名PPS患者在基线时接受了腰穿(LP),而20名接受IVIG治疗的患者在一年后重复了LP。将30例其他神经系统疾病(OND)患者作为对照组。用RT-PCR检测血细胞和CSF细胞中炎性细胞因子TNF,TGFβ,IFNγ,IL-23,IL-13和IL-10。结果与基线和对照组相比,IVIG治疗的患者在一年的随访时间点的SF-36物理成分得分明显更高。与基线相比,IVIG治疗的患者的疼痛VAS评分和6MWT显着改善。与基线时的OND受试者相比,PPS患者的PBMC和CSF中TNF和IFN-γ的相对表达均增加(p <0.05)。 IVIG治疗一年后,PPS患者的脑脊液中IFN-γ和IL23的表达降低,而抗炎性IL-13升高(p <0.05)。结论IVIG对PPS患者的相关QoL变量和炎症细胞因子的影响长达一年。这为在即将进行的这种疗法的试验中安排IVIG提供了基础。

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