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先天性免疫系统与多发性硬化症。复发缓解型多发性硬化症患者缓解期粒细胞数量减少。

Innate Immune System and Multiple Sclerosis. Granulocyte Numbers Are Reduced in Patients Affected by Relapsing-Remitting Multiple Sclerosis during the Remission Phase.

作者信息

Pavelek Zbyšek, Angelucci Francesco, Souček Ondřej, Krejsek Jan, Sobíšek Lukáš, Klímová Blanka, Šarláková Jana, Halúsková Simona, Kuča Kamil, Vališ Martin

机构信息

Department of Neurology, Faculty of Medicine and University Hospital Hradec Králové, Charles University in Prague, Sokolská 581, 500 05 Hradec Kralove, Czech Republic.

Memory Clinic, Department of Neurology, 2nd Faculty of Medicine, Charles University and Motol University Hospital, V Úvalu 84, 150 06 Prague, Czech Republic.

出版信息

J Clin Med. 2020 May 14;9(5):1468. doi: 10.3390/jcm9051468.


DOI:10.3390/jcm9051468
PMID:32422897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7290702/
Abstract

BACKGROUND: Multiple sclerosis (MS) is a neurodegenerative disease that affects the central nervous system. The cause of MS is still unknown, and the role of innate immunity is still poorly understood. OBJECTIVE: The goal of this study was to understand whether, compared to healthy controls, the elements of innate immunity are altered in the blood of MS patients in the remitting phase. METHODS: A total of 77 naïve MS patients and 50 healthy controls were included in this cohort study. Peripheral blood samples were collected and analyzed. All the calculations were performed with the statistical system R (r-project.org). RESULTS: The results showed that MS patients had significantly lower relative representations of granulocytes than healthy controls, while the relative representations of monocytes remained unchanged. CD64- and PD-L1-positive granulocytes exhibited a nonsignificant decreasing trend, while granulocytes with other membrane markers remained noticeably unchanged. CONCLUSION: The results of this study suggest that studies of the causes of MS and its treatment should also be focused on the elements of the innate immune response.

摘要

背景:多发性硬化症(MS)是一种影响中枢神经系统的神经退行性疾病。MS的病因仍不清楚,先天免疫的作用也仍未得到充分理解。 目的:本研究的目的是了解与健康对照相比,缓解期MS患者血液中先天免疫成分是否发生改变。 方法:本队列研究共纳入77例初发MS患者和50例健康对照。采集外周血样本并进行分析。所有计算均使用统计系统R(r-project.org)进行。 结果:结果显示,MS患者粒细胞的相对比例显著低于健康对照,而单核细胞的相对比例保持不变。CD64和PD-L1阳性粒细胞呈现出不显著的下降趋势,而具有其他膜标记物的粒细胞则明显保持不变。 结论:本研究结果表明,对MS病因及其治疗的研究也应关注先天免疫反应的成分。

相似文献

[1]
Innate Immune System and Multiple Sclerosis. Granulocyte Numbers Are Reduced in Patients Affected by Relapsing-Remitting Multiple Sclerosis during the Remission Phase.

J Clin Med. 2020-5-14

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[3]
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[6]
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[7]
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[8]
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[9]
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引用本文的文献

[1]
Unraveling the Role of the Glycogen Synthase Kinase-3β, Bruton's Tyrosine Kinase, and Sphingosine 1 Phosphate Pathways in Multiple Sclerosis.

Endocr Metab Immune Disord Drug Targets. 2024

[2]
Respiratory issues in patients with multiple sclerosis as a risk factor during SARS-CoV-2 infection: a potential role for exercise.

Mol Cell Biochem. 2023-7

[3]
Neutrophils: Underestimated Players in the Pathogenesis of Multiple Sclerosis (MS).

Int J Mol Sci. 2020-6-26

本文引用的文献

[1]
Innate immunity as the trigger of systemic autoimmune diseases.

J Autoimmun. 2020-6

[2]
Multiple Sclerosis.

Adv Exp Med Biol. 2019

[3]
The emerging role of neutrophils in neurodegeneration.

Immunobiology. 2020-1

[4]
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility.

Science. 2019-9-27

[5]
New biological treatments for asthma and skin allergies.

Allergy. 2020-3

[6]
Innate Immune Cells: Monocytes, Monocyte-Derived Macrophages and Microglia as Therapeutic Targets for Alzheimer's Disease and Multiple Sclerosis.

Front Cell Neurosci. 2019-7-31

[7]
Diagnosis and Management of Progressive Multiple Sclerosis.

Biomedicines. 2019-7-29

[8]
Association of circulating anti-CD64 IgM levels with favourable long-term clinical outcomes in multiple sclerosis patients.

J Neuroimmunol. 2019-3-8

[9]
The Emerging Role of Neutrophil Granulocytes in Multiple Sclerosis.

J Clin Med. 2018-12-3

[10]
The roles of macrophages and microglia in multiple sclerosis and experimental autoimmune encephalomyelitis.

J Neuroimmunol. 2018-2-27

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