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多发性硬化症中抗KIR4.1抗体增加:它可能是疾病复发的标志物吗?

Increased anti-KIR4.1 antibodies in multiple sclerosis: could it be a marker of disease relapse?

作者信息

Brill Livnat, Goldberg Lotem, Karni Arnon, Petrou Panayiota, Abramsky Oded, Ovadia Haim, Ben-Hur Tamir, Karussis Dimitrios, Vaknin-Dembinsky Adi

机构信息

Department of Neurology and Laboratory of Neuroimmunology, and the Agnes-Ginges Center for Neurogenetics, Hadassah-Hebrew University Medical Center Jerusalem, Israel.

Neuroimmunology Laboratory, Department of Neurology, Tel Aviv Sourasky Medical Center, and 2Sackler's Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Mult Scler. 2015 Apr;21(5):572-9. doi: 10.1177/1352458514551779. Epub 2014 Nov 12.

Abstract

BACKGROUND

Screening of putative autoimmune targets in multiple sclerosis (MS) revealed a proportion of patients carrying antibodies (Abs) against KIR4.1, a potassium channel that shares functional properties with AQP4. Both are localized at the perivascular astrocytic processes.

AIMS

To measure anti-KIR4.1 Abs in the serum of MS and neuromyelitis optica (NMO) patients, and to identify the clinical and laboratory characteristics of patients harboring anti-KIR4.1 Abs.

METHODS

We measured anti-KIR4.1 Abs in serum, using the peptide KIR4.1 (83-120) enzyme-linked immunosorbent assay (ELISA).

RESULTS

Serum levels of anti-KIR4.1 Abs were significantly higher in MS and NMO patients than in healthy controls (HCs); with Abs detected in 21 of 80, 10 of 45, and 2 of 32 individuals, respectively (MS versus HC, p < 0.05). The level of anti-KIR4.1 Abs was significantly higher during MS relapse, versus remission (p = 0.04). The clinical characteristics of our study patients did not vary based on KIR4.1 positivity.

CONCLUSIONS

Anti-KIR4.1 Abs were found in similar proportions of patients with MS and NMO, at a significantly higher level than observed in HCs; consequently, the presence of Abs does not discriminate between these demyelinating diseases. However, anti-KIR4.1 Ab levels differed in MS patients during relapse and remission; as such, they may represent a marker of disease exacerbation.

摘要

背景

对多发性硬化症(MS)中假定的自身免疫靶点进行筛查时发现,一部分患者携带针对KIR4.1的抗体(Abs),KIR4.1是一种与水通道蛋白4(AQP4)具有相同功能特性的钾通道。两者都定位于血管周围的星形胶质细胞突起。

目的

检测MS和视神经脊髓炎(NMO)患者血清中的抗KIR4.1抗体,并确定携带抗KIR4.1抗体患者的临床和实验室特征。

方法

我们使用肽KIR4.1(83 - 120)酶联免疫吸附测定(ELISA)法检测血清中的抗KIR4.1抗体。

结果

MS和NMO患者血清中的抗KIR4.1抗体水平显著高于健康对照(HCs);在80例MS患者中有21例、45例NMO患者中有10例以及32例健康对照中有2例检测到抗体(MS与HC相比,p < 0.05)。MS复发期的抗KIR4.1抗体水平显著高于缓解期(p = 0.04)。本研究患者的临床特征并未因KIR4.1阳性与否而有所不同。

结论

在MS和NMO患者中发现抗KIR4.1抗体的比例相似,且显著高于健康对照;因此,抗体的存在并不能区分这些脱髓鞘疾病。然而MS患者复发期和缓解期的抗KIR4.1抗体水平有所不同;所以,它们可能代表疾病加重的一个标志物。

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