首页> 外文期刊>Chinese Journal of Contemporary Neurology and Neurosurgery >The study on secretion of cytokine interleukin-4, interleukin-10 and interferon-γ in peripheral blood of multiple sclerosis patients
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The study on secretion of cytokine interleukin-4, interleukin-10 and interferon-γ in peripheral blood of multiple sclerosis patients

机译:多发性硬化症患者外周血细胞因子白细胞介素4,白细胞介素10和干扰素-γ分泌的研究

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Objective Multiple sclerosis (MS) is a mainly cell-mediated autoimmune demyelinating disease in central nervous system (CNS), characterized by inflammatory demyelinating and infiltration of mononuclear cells around microvessels in CNS. It has been shown that MS is caused by the imbalance between T helper cell 1 (Th1) and Th2 or between inflammatory cytokines and anti-inflammatory cytokines. However, the profile of cytokine according to the published data is contradictory. This study is to evaluate the status of cytokines from mononuclear T cells in MS patients and try to provide clues for clinical diagnosis and treatment. Methods Enzyme-linked immunospot assay (ELISPOT) was used to test the spontaneous and antigen-specific [concanavalin A (ConA), myelin basic protein (MBP) and acetyleholine receptor (AChR)] Th1-related cytokine interferon-γ (IFN-γ) and Th2-related cytokines interleukin-4 (IL-4), IL-10 in the peripheral blood mononuclear cells in MS patients, who had not received any immunological treatment over the last 3 months. Results Compared with normal controls and patients with non-immune neurological diseases, MBP specific IL-4, IL-10 and IFN-γ of MS patients increased significantly (P = 0.000, for all). In addition, MBP specific IFN-γ level of MS patients increased signicantly in acute or exacerbating phase when compared with that in stable phase (P = 0.002), while MBP specific IL-4 and IL-10 levels did not differ significantly (P > 0.05, for all). Conclusions The examinations of IL-4, IL-10 and IFN-γ cytokines using ELISPOT are helpful for the differential diagnosis and the disease course of MS.?doi: 10.3969/j.issn.1672-6731.2014.10.008.
机译:目的多发性硬化症(MS)是中枢神经系统(CNS)中一种主要由细胞介导的自身免疫性脱髓鞘疾病,其特征在于炎症性脱髓鞘和单核细胞浸润于CNS中的微血管周围。已经显示MS是由T辅助细胞1(Th1)和Th2之间或炎性细胞因子和抗炎细胞因子之间的不平衡引起的。然而,根据公开的数据,细胞因子的概况是矛盾的。本研究旨在评估MS患者单核T细胞的细胞因子状态,并为临床诊断和治疗提供线索。方法采用酶联免疫斑点法(ELISPOT)检测Th1相关细胞因子干扰素-γ(IFN-γ)的自发性和抗原特异性[伴刀豆球蛋白A(ConA),髓鞘碱性蛋白(MBP)和乙酰胆碱受体(AChR)]。 )和在最近3个月内未接受任何免疫治疗的MS患者外周血单个核细胞中的Th2相关细胞因子白细胞介素4(IL-4),IL-10。结果与正常对照组和非免疫性神经系统疾病患者相比,MS患者的MBP特异性IL-4,IL-10和IFN-γ显着增加(对于所有患者,P = 0.000)。此外,与稳定期相比,MS患者的MBP特异性IFN-γ水平在急性期或加重期显着增加(P = 0.002),而MBP特异性IL-4和IL-10的水平无显着差异(P> 0.05)。结论使用ELISPOT检查IL-4,IL-10和IFN-γ细胞因子有助于MS的鉴别诊断和疾病进程。doi:10.3969 / j.issn.1672-6731.2014.10.008。

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