吉兰-巴雷综合征(GBS)和慢性炎症性脱髓鞘多发性神经病(CIDP)免疫反应相关蛋白的蛋白质组学分析

IF 2.9 4区 医学 Q3 IMMUNOLOGY
Yu-Jing Li , Xue-Yu Zhang , Wen-Jun Zhang , Ya-Li Han , Min-Shu Li , Jian-Li Zhao , Jie Wu , Xiao-Wen Li , Jing Xu , Fu-Dong Shi
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引用次数: 0

摘要

目的是通过高通量分析确定吉兰-巴雷综合征(GBS)和慢性炎症性脱髓鞘性多发性神经病(CIDP)中差异表达蛋白(DEPs)的特征。对 11 名健康对照组(HCs)、21 名 GBS 和 19 名 CIDP 患者的血清进行了 Olink 蛋白质组学分析。在 CIDP 组和 GBS 组的比较中,观察到 ITM2A 上调,NTF4 下调。将 GBS 与 HCs 比较,发现 18 个上调蛋白和 4 个下调蛋白。将 CIDP 与 HCs 进行比较,发现了 15 个上调和 4 个下调的蛋白质。此外,还发现了临床特征与 DEPs 之间的相关性。总之,DEPs 具有巨大的潜力,可促进我们对这些使人衰弱的神经系统疾病发病机制的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteomics analysis of immune response-related proteins in Guillain-Barré Syndrome (GBS) and Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

The objective is to characterize differentially expressed proteins (DEPs) in Guillain-Barré Syndrome (GBS) and Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) through high-throughput analysis. Sera from 11 healthy controls (HCs), 21 GBS and 19 CIDP patients were subjected to Olink Proteomics Analysis. In the comparison between CIDP and GBS groups, up-regulation of ITM2A and down-regulation of NTF4 were observed. Comparing GBS with HCs revealed 18 up-regulated and 4 down-regulated proteins. Comparing CIDP with the HCs identified 15 up-regulated and 4 down-regulated proteins. Additionally, the correlation between clinical characteristics and DEPs were uncovered. In conclusion, the DEPs have significant potential to advance our understanding of the pathogenesis in these debilitating neurological disorders.

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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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