复发缓解型多发性硬化症单核细胞试验研究:与疾病活动的相关性

IF 2.8 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Innate Immunity Pub Date : 2024-07-01 Epub Date: 2024-08-02 DOI:10.1177/17534259241269674
Sara I Taha, Hala Ghareeb Mohamed, Rasha Mamdouh, Nada E Kamal, Shaimaa Sayed Khater
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引用次数: 0

摘要

背景:许多免疫细胞参与了多发性硬化症(MS)的发病。单核细胞被认为是最先进入大脑并引发炎症的细胞。需要更好地了解单核细胞亚型在多发性硬化症中的作用。研究目的本研究旨在调查埃及复发性缓解型多发性硬化症(RRMS)患者中存在的不同单核细胞亚型及其与疾病活动的相关性。研究方法本研究包括44名根据2017年麦克唐纳标准确诊的RRMS患者(22名复发患者,22名缓解患者)和44名匹配的健康对照者。研究人员向患者询问了个人病史和病史,并使用扩展残疾状况量表(EDSS)评估患者的损伤程度。所有参与者的外周血单核细胞亚群的特征均通过流式细胞术确定。结果显示与对照组相比,RRMS 患者经典、中间和非经典单核细胞亚群的百分比显著增加,P 值分别为 0.029、0.049 和 0.043。在 RRMS 患者中,EDSS 评分、病程、过去一年中的复发次数与各种单核细胞亚群的百分比之间没有统计学意义上的相关性(p 值大于 0.05)。此外,缓解期 RRMS 患者和复发期 RRMS 患者各单核细胞亚群的百分比也无明显差异(P 值 >0.05)。然而,磁共振成像(MRI)显示有活动迹象的患者的非典型单核细胞比例明显较高,p 值为 0.002。结论在 RRMS 患者中,无论疾病活动性如何,三个单核细胞亚群(经典、非经典和中间)都会显著增加。这种增加表明单核细胞和先天性免疫在多发性硬化症病理中起着重要作用,尤其是非经典单核细胞亚群。这些研究结果表明,单核细胞可能是一种有前景的多发性硬化症治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A pilot study of monocytes in relapsing remitting multiple sclerosis: Correlation with disease activity.

Background: Numerous immune cells are involved in developing multiple sclerosis (MS). Monocytes are believed to be the first to enter the brain and initiate inflammation. The role of monocyte subtypes in MS needs to be better understood. Objective: The current study aims to investigate the presence of different subsets of monocytes in relapsing-remitting MS (RRMS) Egyptian patients and their correlation with disease activity. Methods: This study included 44 RRMS patients (22 patients in relapse, 22 patients in remission), diagnosed according to the 2017 MacDonalds criteria, and 44 matched healthy controls. Personal and medical histories were taken from the patients, and the Expanded Disability Status Scale (EDSS) was used to evaluate the degree of impairment. Characterization of peripheral blood monocyte subsets was done by flow cytometry for all participants. Results: The percentage of classical, intermediate, and non-classical monocyte subsets showed a significant increase in RRMS patients than controls with p-values of 0.029, 0.049, and 0.043, respectively. In the RRMS patients, there were no statistically significant correlations (p-values >0.05) between the EDSS scores, the duration of disease, and number of relapses in the past year and the percentages of the various monocyte subsets. Furthermore, there were no significant differences in the percentage of each monocyte subset between RRMS patients in remission and those experiencing a relapse (p-values >0.05). However, patients with evidence of activity in magnetic resonance imaging (MRI) had a significantly high percentage of non-classical monocytes with a p-value of 0.002. Conclusion: In RRMS patients, the three monocyte subsets (classical, non-classical and intermediate) increase significantly regardless of the disease activity. This increase denotes the vital role of monocytes and innate immunity in MS pathology, especially the non-classical monocyte subset. These findings suggest that monocytes might be a promising MS therapeutic target.

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来源期刊
Innate Immunity
Innate Immunity 生物-免疫学
CiteScore
7.20
自引率
0.00%
发文量
20
审稿时长
6-12 weeks
期刊介绍: Innate Immunity is a highly ranked, peer-reviewed scholarly journal and is the official journal of the International Endotoxin & Innate Immunity Society (IEIIS). The journal welcomes manuscripts from researchers actively working on all aspects of innate immunity including biologically active bacterial, viral, fungal, parasitic, and plant components, as well as relevant cells, their receptors, signaling pathways, and induced mediators. The aim of the Journal is to provide a single, interdisciplinary forum for the dissemination of new information on innate immunity in humans, animals, and plants to researchers. The Journal creates a vehicle for the publication of articles encompassing all areas of research, basic, applied, and clinical. The subject areas of interest include, but are not limited to, research in biochemistry, biophysics, cell biology, chemistry, clinical medicine, immunology, infectious disease, microbiology, molecular biology, and pharmacology.
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