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多发性硬化症患者小脑广泛的灰质病变与蛛网膜下腔炎症有关。

Extensive grey matter pathology in the cerebellum in multiple sclerosis is linked to inflammation in the subarachnoid space.

作者信息

Howell Owain W, Schulz-Trieglaff Elena Katharina, Carassiti Daniele, Gentleman Steven M, Nicholas Richard, Roncaroli Federico, Reynolds Richard

机构信息

Wolfson Neuroscience Laboratories, Centre for Neuroinflammation and Neurodegeneration, Division of Brain Sciences, Imperial College London, London, UK.

Neurology and Molecular Neuroscience, Institute of Life Science 1, College of Medicine, Swansea University, Swansea, SA2 8PP, UK.

出版信息

Neuropathol Appl Neurobiol. 2015 Oct;41(6):798-813. doi: 10.1111/nan.12199. Epub 2015 May 2.

Abstract

AIMS

Multiple sclerosis (MS) is a progressive inflammatory neurological disease affecting myelin, neurons and glia. Demyelination and neurodegeneration of cortical grey matter contribute to a more severe disease, and inflammation of the forebrain meninges associates with pathology of the underlying neocortical grey matter, particularly in deep sulci. We assessed the extent of meningeal inflammation of the cerebellum, another structure with a deeply folded anatomy, to better understand the association between subarachnoid inflammation and grey matter pathology in progressive MS.

METHODS

We examined demyelinating and neuronal pathology in the context of meningeal inflammation in cerebellar tissue blocks from a cohort of 27 progressive MS cases previously characterized on the basis of the absence/presence of lymphoid-like aggregates in the forebrain meninges, in comparison with 11 non-neurological controls.

RESULTS

Demyelination and meningeal inflammation of the cerebellum was greatest in those cases previously characterized as harbouring lymphoid-like structures in the forebrain regions. Meningeal inflammation was mild to moderate in cerebellar tissue blocks, and no lymphoid-like structures were seen. Quantification of meningeal macrophages, CD4+, CD8+ T lymphocytes, B cells and plasma cells revealed that the density of meningeal macrophages associated with microglial activation in the grey matter, and the extent of grey matter demyelination correlated with the density of macrophages and plasma cells in the overlying meninges, and activated microglia of the parenchyma.

CONCLUSIONS

These data suggest that chronic inflammation is widespread throughout the subarachnoid space and contributes to a more severe subpial demyelinating pathology in the cerebellum.

摘要

目的

多发性硬化症(MS)是一种进行性炎症性神经疾病,会影响髓鞘、神经元和神经胶质。皮质灰质的脱髓鞘和神经变性会导致病情更严重,前脑脑膜的炎症与潜在新皮质灰质的病理变化相关,尤其是在深沟处。我们评估了小脑(另一个解剖结构有深度折叠的部位)脑膜炎症的程度,以更好地了解进行性MS中蛛网膜下腔炎症与灰质病理之间的关联。

方法

我们检查了27例进行性MS病例的小脑组织块中脑膜炎症背景下的脱髓鞘和神经元病理情况,这些病例之前已根据前脑脑膜中是否存在类淋巴样聚集物进行了特征描述,并与11名非神经疾病对照进行了比较。

结果

在那些之前被描述为在前脑区域有类淋巴样结构的病例中,小脑的脱髓鞘和脑膜炎症最为严重。小脑组织块中的脑膜炎症为轻度至中度,未观察到类淋巴样结构。对脑膜巨噬细胞、CD4 +、CD8 + T淋巴细胞、B细胞和浆细胞进行定量分析发现,脑膜巨噬细胞的密度与灰质中的小胶质细胞活化相关,灰质脱髓鞘的程度与上方脑膜中的巨噬细胞和浆细胞密度以及实质中的活化小胶质细胞相关。

结论

这些数据表明,慢性炎症在整个蛛网膜下腔广泛存在,并导致小脑软膜下更严重的脱髓鞘病理变化。

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