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初诊时区分多发性硬化症患者与其他神经系统疾病患者的免疫参数。

Immune Parameters That Distinguish Multiple Sclerosis Patients from Patients with Other Neurological Disorders at Presentation.

作者信息

Mouzaki Athanasia, Rodi Maria, Dimisianos Nikolaos, Emmanuil Andreas, Kalavrizioti Dimitra, Lagoudaki Rosa, Grigoriadis Nikolaos C, Papathanasopoulos Panagiotis

机构信息

Division of Hematology, Department of Internal Medicine, Medical School, University of Patras, Patras, Greece.

Department of Neurology, Patras University Hospital, Patras, Greece.

出版信息

PLoS One. 2015 Aug 28;10(8):e0135434. doi: 10.1371/journal.pone.0135434. eCollection 2015.

Abstract

BACKGROUND/AIM: Multiple sclerosis (MS) is an inflammatory, demyelinating disease of the central nervous system. Effector T helper cells, mainly Th1 and Th17, cytotoxic T-cells, B-cells, macrophages, microglia, and the cytokines they secrete, are implicated in the initiation and maintenance of a deregulated immune response to myelin antigens and the ensuing immune-mediated demyelination. In this study, we investigated whether signature cytokines exist in MS patients at presentation to gain an insight into the underlying immunopathogenic processes at the early stage of the disease.

METHODS

We collected serum and cerebrospinal fluid (CSF) samples from 123 patients at presentation, eventually diagnosed with MS or non-inflammatory (NIND) or inflammatory neurological diseases (IND) or symptomatic controls (SC). The levels of cytokines IFN-γ, TNF-α, TGF-β1, IL-2, IL-4, IL-6, IL-10 and IL-17 were measured, and cytokine ratios, such as Th1/Th2, Th1/Th17, and Type-1/Type-2, were calculated. All parameters were tested for their correlations with the intrathecal IgG synthesis.

RESULTS

Cytokine levels in CSF were lower than in serum in all the patients, with the exception of IL-6. Serum or CSF cytokine levels of MS patients did not differ significantly from NIND or SC, with the exception of serum IFN-γ and TNF-α that were significantly higher in NIND. IND patients presented with the highest levels of all cytokines in serum and CSF, with the exception of serum IL-10 and CSF IL-17. MS patients had a significantly lower serum Th1/Th2 ratio compared to the NIND and IND groups, and significantly lower serum Type-1/Type-2, IFN-γ/IL-10 and CSF Th1/Th17 ratios compared to IND patients. MS patients had a significantly higher CSF IL-17/IL-10 ratio compared to IND patients. The IgG index was higher in MS patients compared to the control groups; the differences reached statistical significance between the MS and the NIND and SC groups. Reiber-Felgenhauer analysis of the QIgG and QAlb indices revealed higher intrathecal IgG synthesis in MS patients, and higher blood-CSF barrier dysfunction in IND patients. The IgG index correlated with CSF IL-4 in MS patients only.

CONCLUSIONS

We found no signature cytokines or profiles thereof in MS patients at presentation. Only IND patients presented with a clear Th1 cytokine polarization in serum and CSF. The parameters that distinguished MS patients from patients with other neurological disorders were IgG intrathecal synthesis, the IgG index and its correlation with CSF IL-4 levels.

摘要

背景/目的:多发性硬化症(MS)是一种中枢神经系统的炎症性脱髓鞘疾病。效应性辅助性T细胞,主要是Th1和Th17、细胞毒性T细胞、B细胞、巨噬细胞、小胶质细胞以及它们分泌的细胞因子,参与了对髓鞘抗原失调的免疫反应的启动和维持以及随之而来的免疫介导的脱髓鞘过程。在本研究中,我们调查了初诊时MS患者是否存在标志性细胞因子,以深入了解疾病早期潜在的免疫致病过程。

方法

我们收集了123例初诊患者的血清和脑脊液(CSF)样本,这些患者最终被诊断为MS、非炎性(NIND)或炎性神经系统疾病(IND)或症状性对照(SC)。检测了细胞因子IFN-γ、TNF-α、TGF-β1、IL-2、IL-4、IL-6、IL-10和IL-17的水平,并计算了细胞因子比率,如Th1/Th2、Th1/Th17和1型/2型。测试了所有参数与鞘内IgG合成的相关性。

结果

除IL-6外,所有患者脑脊液中的细胞因子水平均低于血清。MS患者的血清或脑脊液细胞因子水平与NIND或SC患者无显著差异,除了NIND患者血清中的IFN-γ和TNF-α显著更高。IND患者血清和脑脊液中所有细胞因子水平最高,血清IL-10和脑脊液IL-17除外。与NIND和IND组相比,MS患者的血清Th1/Th2比率显著更低,与IND患者相比,血清1型/2型、IFN-γ/IL-10和脑脊液Th1/Th17比率显著更低。与IND患者相比,MS患者的脑脊液IL-17/IL-10比率显著更高。与对照组相比,MS患者的IgG指数更高;MS与NIND和SC组之间的差异具有统计学意义。对QIgG和QAlb指数的Reiber-Felgenhauer分析显示,MS患者鞘内IgG合成更高,IND患者血脑屏障功能障碍更严重。IgG指数仅与MS患者脑脊液中的IL-4相关。

结论

我们在初诊时的MS患者中未发现标志性细胞因子或其特征。只有IND患者在血清和脑脊液中呈现明显的Th1细胞因子极化。区分MS患者与其他神经系统疾病患者的参数是鞘内IgG合成、IgG指数及其与脑脊液IL-4水平的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8648/4552669/bb367ba4721a/pone.0135434.g001.jpg

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