感染、疫苗接种和 1 型嗜睡症:证据和潜在的分子机制

IF 2.9 4区 医学 Q3 IMMUNOLOGY
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引用次数: 0

摘要

NT1 是一种罕见的慢性致残性神经系统疾病,可导致白天过度嗜睡和惊厥。NT1的病理特征是下丘脑外侧产生视网膜下素(HCRT)/神经肽的神经元几乎完全丧失。虽然 NT1 的确切病因尚不清楚,但许多研究提供了令人信服的证据,支持其源于自身免疫。关于 NT1 发病机制的主流假设观点认为,免疫介导的 HCRT 神经元缺失可通过接种 Pandemrix® 疫苗和/或感染遗传易感患者(特别是 HLA-DQB1*06:02 MHC II 类等位基因携带者)而触发。感染/接种可诱发 NT1 自身免疫的分子机制仍有待阐明。在本综述中,将结合其他自身免疫性疾病的现有研究结果,讨论有关疫苗接种和感染的证据,以及疫苗接种和感染可能与 NT1 发病机制有关的潜在机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Infection, vaccination and narcolepsy type 1: Evidence and potential molecular mechanisms

NT1 is a rare, chronic and disabling neurological disease causing excessive daytime sleepiness and cataplexy. NT1 is characterized pathologically by an almost complete loss of neurons producing the hypocretin (HCRT)/orexin neuropeptides in the lateral hypothalamus. While the exact etiology of NT1 is still unknown, numerous studies have provided compelling evidence supporting its autoimmune origin. The prevailing hypothetical view on the pathogenesis of NT1 involves an immune-mediated loss of HCRT neurons that can be triggered by Pandemrix® vaccination and/or by infection in genetically susceptible patients, specifically carriers of the HLA-DQB1*06:02 MHC class II allele. The molecular mechanisms by which infection/vaccination can induce autoimmunity in the case of NT1 remain to be elucidated. In this review, evidence regarding the involvement of vaccination and infection and the potential mechanisms by which it could be linked to the pathogenesis of NT1 will be discussed in light of the existing findings in other autoimmune diseases.

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来源期刊
Journal of neuroimmunology
Journal of neuroimmunology 医学-免疫学
CiteScore
6.10
自引率
3.00%
发文量
154
审稿时长
37 days
期刊介绍: The Journal of Neuroimmunology affords a forum for the publication of works applying immunologic methodology to the furtherance of the neurological sciences. Studies on all branches of the neurosciences, particularly fundamental and applied neurobiology, neurology, neuropathology, neurochemistry, neurovirology, neuroendocrinology, neuromuscular research, neuropharmacology and psychology, which involve either immunologic methodology (e.g. immunocytochemistry) or fundamental immunology (e.g. antibody and lymphocyte assays), are considered for publication.
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