首页> 美国卫生研究院文献>Frontiers in Immunology >Meningeal Tertiary Lymphoid Tissues and Multiple Sclerosis: A Gathering Place for Diverse Types of Immune Cells during CNS Autoimmunity
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Meningeal Tertiary Lymphoid Tissues and Multiple Sclerosis: A Gathering Place for Diverse Types of Immune Cells during CNS Autoimmunity

机译:脑膜三级淋巴组织和多发性硬化:在中枢神经系统自身免疫过程中免疫细胞的各种类型的聚集地。

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摘要

Collections of leukocytes in the meningeal space have been documented in Multiple Sclerosis (MS). These meningeal aggregates, which in the context of other autoimmune diseases have often been termed tertiary lymphoid tissues (TLT), have been associated with sub-pial cortical damage and disease progression. However, the key molecular and cellular signals required for their formation and maintenance remain unclear. Herein, we review TLT structures in other disease states in order to provide a framework for understanding these structures in the MS meninges. We then assess the evidence that the meningeal compartment serves as an important nexus for immune cells as well as a location for drainage of antigen into cervical lymph nodes. Extrapolating what is known about the molecular and cellular cues that initiate the formation of leukocyte aggregates in non-lymphoid tissues, we speculate on what signals lead to the formation and maintenance of meningeal TLT structures. Referring to the animal model of MS [experimental autoimmune encephalomyelitis (EAE)], we also explore what is known about these structures in supporting B cell and T cell responses during neuroinflammation. Last, we examine the evidence that connects these structures to ongoing neuropathology. Collectively, our review points to the meningeal compartment as an important player in neuroinflammatory processes. Moreover, we hypothesize that in order to gain insights into pro- and anti-inflammatory properties of lymphocytes in MS, one must understand the cellular scaffolds that support lymphocyte retention within the meninges, thus highlighting the importance of non-immune cells (stromal cells) in the neuroinflammatory process.
机译:在多发性硬化症(MS)中已记录了脑膜空间中白细胞的收集。这些脑膜聚集体在其他自身免疫性疾病中常被称为三级淋巴组织(TLT),与脊髓下皮质损伤和疾病进展相关。但是,尚不清楚其形成和维持所需的关键分子和细胞信号。在此,我们回顾了其他疾病状态下的TLT结构,以提供一个理解MS脑膜中这些结构的框架。然后,我们评估了脑膜隔室充当免疫细胞的重要纽带以及抗原排入宫颈淋巴结的位置的证据。推断关于引发非淋巴组织中白细胞聚集体形成的分子和细胞线索的已知信息,我们推测是什么信号导致了脑膜TLT结构的形成和维持。参考MS [实验性自身免疫性脑脊髓炎(EAE)]的动物模型,我们还探索了有关这些结构在神经炎症过程中支持B细胞和T细胞反应的已知知识。最后,我们研究了将这些结构与正在进行的神经病理学联系起来的证据。总的来说,我们的评论指出脑膜隔室是神经炎症过程中的重要角色。此外,我们假设,为了深入了解MS中淋巴细胞的促炎和抗炎特性,必须了解支持脑膜内淋巴细胞滞留的细胞支架,从而强调非免疫细胞(基质细胞)的重要性在神经炎症过程中。

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