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本文引用的文献

1
Astrocytic autoantibody of neuromyelitis optica (NMO-IgG) binds to aquaporin-4 extracellular loops, monomers, tetramers and high order arrays.视神经脊髓炎自身抗体(NMO-IgG)与水通道蛋白-4 胞外环、单体、四聚体和高级别多聚体结合。
J Autoimmun. 2013 Feb;40:21-7. doi: 10.1016/j.jaut.2012.07.008. Epub 2012 Aug 18.
2
Aquaporin 4-specific T cells in neuromyelitis optica exhibit a Th17 bias and recognize Clostridium ABC transporter.视神经脊髓炎中的水通道蛋白 4 特异性 T 细胞表现出 Th17 偏向,并识别梭菌 ABC 转运蛋白。
Ann Neurol. 2012 Jul;72(1):53-64. doi: 10.1002/ana.23651. Epub 2012 Jul 17.
3
Increased T-cell immunity against aquaporin-4 and proteolipid protein in neuromyelitis optica.视神经脊髓炎中 T 细胞对水通道蛋白 4 和髓鞘相关糖蛋白的免疫应答增强。
Int Immunol. 2011 Sep;23(9):565-73. doi: 10.1093/intimm/dxr056. Epub 2011 Jul 27.
4
Overexpression of the dominant-negative form of interferon regulatory factor 1 in oligodendrocytes protects against experimental autoimmune encephalomyelitis.少突胶质细胞中干扰素调节因子 1 的显性负突变体的过度表达可预防实验性自身免疫性脑脊髓炎。
J Neurosci. 2011 Jun 8;31(23):8329-41. doi: 10.1523/JNEUROSCI.1028-11.2011.
5
Interferon-β exacerbates Th17-mediated inflammatory disease.干扰素-β加重 Th17 介导的炎症性疾病。
Trends Immunol. 2011 Jun;32(6):272-7. doi: 10.1016/j.it.2011.03.008. Epub 2011 Apr 29.
6
Increased memory Th17 cells in patients with neuromyelitis optica and multiple sclerosis.视神经脊髓炎和多发性硬化患者记忆性 Th17 细胞增加。
J Neuroimmunol. 2011 May;234(1-2):155-60. doi: 10.1016/j.jneuroim.2011.03.009. Epub 2011 Apr 12.
7
Pathogenic T cell responses against aquaporin 4.针对水通道蛋白 4 的致病性 T 细胞反应。
Acta Neuropathol. 2011 Jul;122(1):21-34. doi: 10.1007/s00401-011-0824-0. Epub 2011 Apr 6.
8
IRF-1 signaling in central nervous system glial cells regulates inflammatory demyelination.IRF-1 信号在中枢神经系统胶质细胞中调节炎症性脱髓鞘。
J Neuroimmunol. 2011 Apr;233(1-2):147-59. doi: 10.1016/j.jneuroim.2011.01.001. Epub 2011 Jan 22.
9
Immunodominant T cell determinants of aquaporin-4, the autoantigen associated with neuromyelitis optica.水通道蛋白 4 的免疫优势 T 细胞决定簇,该蛋白是与视神经脊髓炎相关的自身抗原。
PLoS One. 2010 Nov 30;5(11):e15050. doi: 10.1371/journal.pone.0015050.
10
Anti-tuberculosis treatment for Devic's neuromyelitis optica.抗结核治疗视神经脊髓炎。
J Clin Neurosci. 2010 Nov;17(11):1372-7. doi: 10.1016/j.jocn.2010.02.023. Epub 2010 Aug 9.

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.

DOI:10.4049/jimmunol.1200486
PMID:23008451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3586280/
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。