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梅尼埃病中的细胞因子与炎症

Cytokines and Inflammation in Meniere Disease.

作者信息

Frejo Lidia, Lopez-Escamez Jose Antonio

机构信息

Otology and Neurotology Group CTS495, Department of Genomic Medicine, Centre for Genomics and Oncological Research (GENYO), Pfizer-University of Granada-Junta de Andalucía, PTS, Granada, Spain.

Department of Otolaryngology, Instituto de Investigación Biosanitaria ibs. Granada, Hospital Universitario Virgen de las Nieves, Granada, Spain.

出版信息

Clin Exp Otorhinolaryngol. 2022 Feb;15(1):49-59. doi: 10.21053/ceo.2021.00920. Epub 2022 Feb 8.

Abstract

Meniere disease (MD) is a rare set of conditions associated with the accumulation of endolymph in the cochlear duct and the vestibular labyrinth with a decrease of endocochlear potential. It is considered a chronic inflammatory disorder of the inner ear with a multifactorial origin. The clinical syndrome includes several groups of patients with a core phenotype: sensorineural hearing loss, episodes of vertigo, and tinnitus with a non-predictable course. Genetic factors and the innate immune response seem to play a central role in the pathophysiology of the condition. Autoimmune MD should be diagnosed if a patient fulfills the diagnostic criteria for MD and one of the following autoimmune disorders: autoimmune thyroid disease, psoriasis, autoimmune arthritis, ankylosing spondylitis, or systemic lupus erythematosus. We summarize the evidence to support autoimmune MD as an endophenotype in bilateral MD associated with the allelic variant rs4947296 and nuclear factor-kappa B (NF-κB)-mediated inflammation, the role of cytokines (particularly interleukin-1β and tumor necrosis factor-α) in defining a subset of patients with autoinflammation, and the potential role of cytokines as biomarkers to distinguish between patients with MD and vestibular migraine. Finally, we also introduce a list of potential drugs that could regulate the immune response in MD with potential for repurposing in clinical trials.

摘要

梅尼埃病(MD)是一组罕见的病症,与内淋巴在蜗管和前庭迷路中的积聚以及内耳蜗电位降低有关。它被认为是一种具有多因素起源的内耳慢性炎症性疾病。临床综合征包括几组具有核心表型的患者:感音神经性听力损失、眩晕发作和耳鸣,病程不可预测。遗传因素和先天性免疫反应似乎在该病症的病理生理学中起核心作用。如果患者符合MD的诊断标准以及以下自身免疫性疾病之一:自身免疫性甲状腺疾病、银屑病、自身免疫性关节炎、强直性脊柱炎或系统性红斑狼疮,则应诊断为自身免疫性MD。我们总结了支持自身免疫性MD作为与等位基因变体rs4947296和核因子-κB(NF-κB)介导的炎症相关的双侧MD中的一种内表型的证据,细胞因子(特别是白细胞介素-1β和肿瘤坏死因子-α)在定义一部分自身炎症患者中的作用,以及细胞因子作为区分MD患者和前庭性偏头痛患者的生物标志物的潜在作用。最后,我们还介绍了一系列可能调节MD免疫反应并有可能在临床试验中重新利用的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf26/8901949/be0bbc23c91e/ceo-2021-00920f1.jpg

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