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细菌水通道蛋白 Z 与人水通道蛋白 4 之间的交叉免疫反应:对视神经脊髓炎的潜在相关性。

Cross-immunoreactivity between bacterial aquaporin-Z and human aquaporin-4: potential relevance to neuromyelitis optica.

机构信息

Department of Neurological Sciences, Multiple Sclerosis Center, Rush University Medical Center, Chicago, IL 60612, USA.

出版信息

J Immunol. 2012 Nov 1;189(9):4602-11. doi: 10.4049/jimmunol.1200486. Epub 2012 Sep 24.

Abstract

Neuromyelitis optica (NMO) is a chronic inflammatory disease of the CNS that is mediated, in part, by a self-reactive Ab against the astrocyte aquaporin-4 protein. In the current study, we examined the possibility and the biological significance of cross-immunoreactivity between bacterial aquaporin-Z and human aquaporin-4 proteins. Sequence-alignment analysis of these proteins revealed several regions of significant structural homology. Some of the homologous regions were also found to overlap with important immune and disease-relevant epitopes. Cross-immunoreactivity between aquaporin-Z and aquaporin-4 was investigated and ascertained in multiple immune-based assays using sera from patients with neuromyelitis optica, immune mouse serum, and Abs raised against aquaporin-Z. The biological significance of this phenomenon was established in series of experiments demonstrating that induction of an immune response against aquaporin-Z or its homologous regions can also trigger an autoimmune reaction against aquaporin-4 and inflammation of the CNS. Our study indicates that the autoimmune response against aquaporin-4 in neuromyelitis optica may be triggered by infection-induced cross-immunoreactivity and presents a new perspective on the pathogenesis of this disease.

摘要

视神经脊髓炎(NMO)是一种中枢神经系统的慢性炎症性疾病,部分由针对星形胶质细胞水通道蛋白-4 蛋白的自身反应性抗体介导。在本研究中,我们研究了细菌水通道蛋白-Z 与人类水通道蛋白-4 蛋白之间发生交叉免疫反应的可能性和生物学意义。对这些蛋白质的序列比对分析显示出几个具有显著结构同源性的区域。一些同源区域也与重要的免疫和疾病相关表位重叠。使用来自视神经脊髓炎患者的血清、免疫鼠血清和针对水通道蛋白-Z 的抗体,在多种基于免疫的检测中研究和确定了水通道蛋白-Z 和水通道蛋白-4 之间的交叉免疫反应性。通过一系列实验证明了这一现象的生物学意义,这些实验表明,针对水通道蛋白-Z 或其同源区域的免疫反应的诱导也可以引发针对水通道蛋白-4 的自身免疫反应和中枢神经系统炎症。我们的研究表明,视神经脊髓炎中水通道蛋白-4 的自身免疫反应可能是由感染诱导的交叉免疫反应触发的,这为该疾病的发病机制提供了新的视角。

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