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抗原在神经元中的呈现及其在帕金森病中的可能作用。

Neuronal Presentation of Antigen and Its Possible Role in Parkinson's Disease.

机构信息

Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA.

Department of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.

出版信息

J Parkinsons Dis. 2022;12(s1):S137-S147. doi: 10.3233/JPD-223153.

Abstract

Patients with Parkinson's disease (PD) and other synucleinopathies often exhibit autoimmune features, including CD4+ and some CD8+ T lymphocytes that recognize epitopes derived from alpha-synuclein. While neurons have long been considered to not present antigens, recent data indicate that they can be induced to do so, particularly in response to interferons and other forms of stress. Here, we review literature on neuronal antigen presentation and its potential role in PD. Although direct evidence for CD8+ T cell-mediated neuronal death is lacking in PD, neuronal antigen presentation appears central to the pathology of Rasmussen's encephalitis, a pediatric neurological disorder driven by cytotoxic T cell infiltration and neuroinflammation. Emerging data suggest that T cells enter the brain in PD and other synucleinopathies, where the majority of neuromelanin-containing substantia nigra and locus coeruleus neurons express MHC Class I molecules. In cell culture, CD8+ T cell recognition of antigen:MHC Class I complexes on neuronal membranes leads to cytotoxic responses and neuronal cell death. Recent animal models suggest the possibility of T cell autoreactivity to mitochondrial antigens in PD. It remains unclear if neuronal antigen presentation plays a role in PD or other neurodegenerative disorders, and efforts are underway to better elucidate the potential impact of autoimmune responses on neurodegeneration.

摘要

帕金森病(PD)和其他突触核蛋白病患者常表现出自免疫特征,包括识别来自α-突触核蛋白的表位的 CD4+和一些 CD8+T 淋巴细胞。虽然神经元长期以来被认为不呈现抗原,但最近的数据表明,它们可以被诱导呈现抗原,特别是在干扰素和其他形式的应激下。在这里,我们回顾了关于神经元抗原呈递及其在 PD 中的潜在作用的文献。尽管 PD 中缺乏 CD8+T 细胞介导的神经元死亡的直接证据,但神经元抗原呈递似乎是 Rasmussen 脑炎病理的核心,Rasmussen 脑炎是一种由细胞毒性 T 细胞浸润和神经炎症驱动的儿科神经障碍。新出现的数据表明,T 细胞进入 PD 和其他突触核蛋白病的大脑,在那里大多数含有神经黑色素的黑质和蓝斑神经元表达 MHC 类 I 分子。在细胞培养中,CD8+T 细胞对神经元膜上抗原:MHC 类 I 复合物的识别导致细胞毒性反应和神经元细胞死亡。最近的动物模型表明 PD 中存在 T 细胞自身反应性针对线粒体抗原的可能性。目前尚不清楚神经元抗原呈递是否在 PD 或其他神经退行性疾病中起作用,并且正在努力更好地阐明自身免疫反应对神经退行性变的潜在影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ecf/9535583/05bdf2e687ad/jpd-12-jpd223153-g001.jpg

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