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本文引用的文献

1
The Probable Infectious Origin of Multiple Sclerosis.多发性硬化症可能的感染起源
NeuroSci. 2023 Sep 7;4(3):211-234. doi: 10.3390/neurosci4030019. eCollection 2023 Sep.
2
Multiple Sclerosis: Inflammatory and Neuroglial Aspects.多发性硬化症:炎症与神经胶质方面
Curr Issues Mol Biol. 2023 Feb 8;45(2):1443-1470. doi: 10.3390/cimb45020094.
3
The Immune Response in Multiple Sclerosis.多发性硬化症中的免疫反应。
Annu Rev Pathol. 2022 Jan 24;17:121-139. doi: 10.1146/annurev-pathol-052920-040318. Epub 2021 Oct 4.
4
High Resolution Haplotype Analyses of Classical HLA Genes in Families With Multiple Sclerosis Highlights the Role of HLA-DP Alleles in Disease Susceptibility.高分辨率单体型分析多发性硬化症家系中的经典 HLA 基因,突出了 HLA-DP 等位基因在疾病易感性中的作用。
Front Immunol. 2021 May 25;12:644838. doi: 10.3389/fimmu.2021.644838. eCollection 2021.
5
Targeted Expression of Myelin Autoantigen in the Periphery Induces Antigen-Specific T and B Cell Tolerance and Ameliorates Autoimmune Disease.外周组织中髓鞘自身抗原的靶向表达诱导抗原特异性 T 和 B 细胞耐受,并改善自身免疫性疾病。
Front Immunol. 2021 Jun 2;12:668487. doi: 10.3389/fimmu.2021.668487. eCollection 2021.
6
Class II HLA (DRB1, & DQB1) alleles and IL7R (rs6897932) variants and the risk for Multiple Sclerosis in Kerala, India.印度喀拉拉邦的II类人类白细胞抗原(DRB1和DQB1)等位基因、白细胞介素7受体(rs6897932)变体与多发性硬化症风险
Mult Scler Relat Disord. 2021 May;50:102848. doi: 10.1016/j.msard.2021.102848. Epub 2021 Feb 20.
7
Th17 and Cognitive Impairment: Possible Mechanisms of Action.辅助性T细胞17与认知障碍:可能的作用机制
Front Neuroanat. 2019 Nov 19;13:95. doi: 10.3389/fnana.2019.00095. eCollection 2019.
8
Midbrain microglia mediate a specific immunosuppressive response under inflammatory conditions.中脑小胶质细胞在炎症条件下介导一种特定的免疫抑制反应。
J Neuroinflammation. 2019 Nov 22;16(1):233. doi: 10.1186/s12974-019-1628-8.
9
Environmental and genetic risk factors for MS: an integrated review.MS 的环境和遗传风险因素:综合述评。
Ann Clin Transl Neurol. 2019 Sep;6(9):1905-1922. doi: 10.1002/acn3.50862. Epub 2019 Aug 7.
10
Next-generation sequencing identifies contribution of both class I and II HLA genes on susceptibility of multiple sclerosis in Japanese.下一代测序鉴定出 class I 和 II HLA 基因对日本人多发性硬化易感性的贡献。
J Neuroinflammation. 2019 Aug 5;16(1):162. doi: 10.1186/s12974-019-1551-z.

罗马尼亚患者多发性硬化症的免疫遗传学:初步数据。

Immunogenetics of Multiple Sclerosis in Romanian Patients: Preliminary Data.

作者信息

Constantinescu Alexandra Elena, Mărunțelu Ion, Pleșa Andreea, Sîrbu Carmen Adella, Pleșa Florentina Cristina, Constantinescu Andreia Ioana, Constantinescu Ileana

机构信息

Faculty of Medicine, "Carol Davila" Medical University Bucharest, 020021 Bucharest, Romania.

"Emil Palade" Center of Excellence for Young People in Scientific Research (EP-CEYR), Academy of Romanian Scientists, 030167 Bucharest, Romania.

出版信息

Int J Mol Sci. 2025 Aug 6;26(15):7628. doi: 10.3390/ijms26157628.

DOI:10.3390/ijms26157628
PMID:40806754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12347847/
Abstract

Multiple sclerosis (MS) is a chronic autoimmune disease characterized by the immune system attacking the central nervous system, leading to demyelination and neurodegeneration. This work investigates the relationship between specific human leukocyte antigen (HLA) polymorphisms and MS, aiming to reveal the immunogenetic background of this disease for more individualized management approaches. This study employed a case-control design, analyzing HLA allele frequencies in 179 MS patients and 200 control subjects using next-generation sequencing, The key findings indicate significant associations between several HLA Class I and II alleles and MS, including HLA-B35:03:01:03, HLA-C04:01:01:14, HLA-DRB115:01:01:26, and HLA-DQA105:05:01:02. These findings emphasize the critical role of HLA molecules in MS Romanian patients.

摘要

多发性硬化症(MS)是一种慢性自身免疫性疾病,其特征是免疫系统攻击中枢神经系统,导致脱髓鞘和神经退行性变。这项工作研究了特定人类白细胞抗原(HLA)多态性与MS之间的关系,旨在揭示这种疾病的免疫遗传背景,以实现更个性化的管理方法。本研究采用病例对照设计,使用下一代测序分析了179例MS患者和200例对照受试者的HLA等位基因频率。关键发现表明,几种HLA I类和II类等位基因与MS之间存在显著关联,包括HLA-B35:03:01:03、HLA-C04:01:01:14、HLA-DRB115:01:01:26和HLA-DQA105:05:01:02。这些发现强调了HLA分子在罗马尼亚MS患者中的关键作用。