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多发性硬化症:未经治疗的患者中分泌白细胞介素-10的血液单核细胞水平较低,但在β-干扰素-1b治疗期间会升高。

Multiple sclerosis: levels of interleukin-10-secreting blood mononuclear cells are low in untreated patients but augmented during interferon-beta-1b treatment.

作者信息

Ozenci V, Kouwenhoven M, Huang Y M, Xiao B, Kivisäkk P, Fredrikson S, Link H

机构信息

Division of Neurology, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden.

出版信息

Scand J Immunol. 1999 May;49(5):554-61. doi: 10.1046/j.1365-3083.1999.00546.x.

DOI:10.1046/j.1365-3083.1999.00546.x
PMID:10320650
Abstract

The cytokine interleukin (IL)-10 has immune response down-regulatory properties, which include suppression of the synthesis of pro-inflammatory cytokines such as interferon (IFN)-gamma and of major histocompatibility complex (MHC) class II expression on monocytes. To further elucidate the involvement of IL-10 in multiple sclerosis (MS), an enzyme-linked immunospot assay was adopted to enumerate IL-10-secreting mononuclear cells (MNC) in peripheral blood. IFN-gamma secreting MNC were detected in parallel. Levels of IL-10-secreting cells were lower in patients with MS compared with other neurological diseases (OND) and healthy subjects. This difference was seen only in patients with untreated MS, and not in those undergoing treatment with IFN-beta-1b. No differences were observed when subgrouping the patients with MS regarding clinical phase (exacerbation, remission, secondary progression), duration of MS or disability status. Levels of IFN-gamma-secreting blood MNC did not differ in patients with MS, irrespective of treatment with IFN-beta-1b, compared with OND and healthy subjects. Patients with MS, but not the two groups of controls, had elevated numbers of IL-10- and IFN-gamma-secreting cells upon stimulation with MBP compared with culture in the absence of antigen. The data suggest that IL-10 is decreased in MS and that treatment resulting in its up-regulation beneficially influence the disease.

摘要

细胞因子白细胞介素(IL)-10具有免疫反应下调特性,其中包括抑制促炎细胞因子如干扰素(IFN)-γ的合成以及单核细胞上主要组织相容性复合体(MHC)II类分子的表达。为了进一步阐明IL-10在多发性硬化症(MS)中的作用,采用酶联免疫斑点法来计数外周血中分泌IL-10的单核细胞(MNC)。同时检测分泌IFN-γ的MNC。与其他神经系统疾病(OND)患者和健康受试者相比,MS患者中分泌IL-10的细胞水平较低。这种差异仅在未经治疗的MS患者中出现,而在接受β-1b干扰素治疗的患者中未出现。根据临床阶段(加重期、缓解期、继发进展期)、MS病程或残疾状态对MS患者进行亚组分析时,未观察到差异。与OND患者和健康受试者相比,无论是否接受β-1b干扰素治疗,MS患者分泌IFN-γ的血液MNC水平均无差异。与在无抗原培养条件下相比,用髓鞘碱性蛋白(MBP)刺激后,MS患者(而非两组对照)分泌IL-10和IFN-γ的细胞数量增加。数据表明,MS中IL-10减少,导致其上调的治疗对该疾病有有益影响。

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