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多发性硬化症患者脑脊液中CD4+ CD25+调节性T细胞频率增加,但血液中未增加。

Increased frequency of CD4+ CD25+ regulatory T cells in the cerebrospinal fluid but not in the blood of multiple sclerosis patients.

作者信息

Feger U, Luther C, Poeschel S, Melms A, Tolosa E, Wiendl H

机构信息

Department of General Neurology, Hertie Institute for Clinical Brain Research, University of Tübingen, Germany.

出版信息

Clin Exp Immunol. 2007 Mar;147(3):412-8. doi: 10.1111/j.1365-2249.2006.03271.x.

DOI:10.1111/j.1365-2249.2006.03271.x
PMID:17302889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1810482/
Abstract

Naturally occurring CD4+ CD25+ regulatory T cells (nTreg) play a major role in controlling autoimmunity by suppressing self-reactive T cells. Multiple sclerosis (MS) is an inflammatory demyelinating disorder of the central nervous system (CNS), where T cells play a key role in orchestrating tissue damage. While CD4+ CD25+ nTreg have been investigated in peripheral blood from MS patients, little is known about their presence and possible function within the target organ, the CNS. In order to study whether these cells are present in the cerebrospinal fluid (CSF) under pathological conditions, we have analysed the frequency of CD4+ CD25+ nTreg in peripheral blood and CSF from MS patients (n=14), patients with other neurological disorders (OND; n=9) and compared peripheral levels with healthy controls (n=40). We found that the frequency of CD4+ CD25+ forkhead transcription factor 3 (FOXP3)+ nTreg was significantly elevated in the CSF from MS patients (mean CSF=4 x 05 +/- 1.54% versus mean peripheral blood = 2 x 93 +/- 0 x 94%) but not from patients with other neurological disorders (mean CSF = 3 x 78 +/- 1 x 26% versus mean peripheral blood = 3 x 74 +/- 1 x 4%). The frequency of nTreg in the periphery did not differ between MS patients and healthy donors; however, nTreg from MS patients showed reduced suppressive capacity.

摘要

天然存在的CD4+ CD25+调节性T细胞(nTreg)通过抑制自身反应性T细胞在控制自身免疫中发挥主要作用。多发性硬化症(MS)是一种中枢神经系统(CNS)的炎性脱髓鞘疾病,其中T细胞在组织损伤的发生过程中起关键作用。虽然已经对MS患者外周血中的CD4+ CD25+ nTreg进行了研究,但对于它们在靶器官CNS中的存在情况及其可能的功能却知之甚少。为了研究在病理条件下这些细胞是否存在于脑脊液(CSF)中,我们分析了MS患者(n = 14)、其他神经系统疾病(OND;n = 9)患者外周血和CSF中CD4+ CD25+ nTreg的频率,并将外周水平与健康对照者(n = 40)进行了比较。我们发现,MS患者CSF中CD4+ CD25+叉头转录因子3(FOXP3)+ nTreg的频率显著升高(平均CSF = 4×05±1.54%,而平均外周血 = 2×93±0×94%),但其他神经系统疾病患者则不然(平均CSF = 3×78±1×26%,而平均外周血 = 3×74±1×4%)。MS患者和健康供体外周血中nTreg的频率没有差异;然而,MS患者的nTreg显示出抑制能力降低。

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本文引用的文献

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Circulating dendritic cells subsets and regulatory T-cells at multiple sclerosis relapse: differential short-term changes on corticosteroids therapy.多发性硬化症复发时循环树突状细胞亚群和调节性T细胞:皮质类固醇治疗的短期差异变化
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Secondary progressive in contrast to relapsing-remitting multiple sclerosis patients show a normal CD4+CD25+ regulatory T-cell function and FOXP3 expression.与复发缓解型多发性硬化症患者相比,继发进展型患者表现出正常的CD4+CD25+调节性T细胞功能和FOXP3表达。
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Foxp3+ CD25- CD4 T cells constitute a reservoir of committed regulatory cells that regain CD25 expression upon homeostatic expansion.Foxp3+ CD25- CD4 T细胞构成了一群定向调节性细胞库,这些细胞在稳态扩增时会重新表达CD25。
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Circulating CD4+CD25+ T regulatory cells are not altered in multiple sclerosis and unaffected by disease-modulating drugs.循环中的CD4+CD25+ T调节细胞在多发性硬化症中未发生改变,且不受疾病调节药物的影响。
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Human cerebrospinal fluid central memory CD4+ T cells: evidence for trafficking through choroid plexus and meninges via P-selectin.人脑脊液中枢记忆性CD4 + T细胞:通过P-选择素经脉络丛和脑膜迁移的证据。
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Nat Immunol. 2003 Apr;4(4):330-6. doi: 10.1038/ni904. Epub 2003 Mar 3.