Proteomic profile of extracellular vesicles from plasma and CSF of multiple sclerosis patients reveals disease activity-associated EAAT2.

IF 9.3 1区 医学 Q1 IMMUNOLOGY
Antonella D'Ambrosio, Silvia Zamboni, Serena Camerini, Marialuisa Casella, Massimo Sanchez, Donatella Pietraforte, Nicola Vanacore, Marco Diociauti, Marta Altieri, Vittorio Di Piero, Ada Francia, Simona Pontecorvo, Marco Puthenparampil, Paolo Gallo, Paola Margutti
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引用次数: 0

Abstract

Background and objectives: There is an urgent need to discover blood-based biomarkers of multiple sclerosis (MS) to better define the underlying biology of relapses and monitor disease progression. The main goal of this study is to search for candidate biomarkers of MS relapses associated with circulating extracellular vesicles (EVs), an emerging tool for biomarker discovery.

Methods: EVs, purified from unpaired plasma and CSF samples of RRMS patients by size-exclusion chromatography (SEC), underwent proteomic analysis to discover novel biomarkers associated with MS relapses. The candidate biomarkers of disease activity were detected by comparison approach between plasma- and CSF-EV proteomes associated with relapses. Among them, a selected potential biomarker was evaluated in a cohort of MS patients, using a novel and highly reproducible flow cytometry-based approach in order to detect low abundant EV subsets in a complex body fluid such as plasma.

Results: The proteomic profiles of both SEC-purified plasma EVs (from 6 patients in relapse and 5 patients in remission) and SEC-purified CSF EVs (from 4 patients in relapse and 3 patients in remission) revealed a set of proteins associated with MS relapses significant enriched in the synaptic transmission pathway. Among common proteins, excitatory amino-acid transporter 2, EAAT2, responsible for the majority of the glutamate uptake in CNS, was worthy of further investigation. By screening plasma samples from 110 MS patients, we found a significant association of plasma EV-carried EAAT2 protein (EV-EAAT2) with MS relapses, regardless of disease-modifying therapies. This finding was confirmed by investigating the presence of EV-EAAT2 in plasma samples collected longitudinally from 10 RRMS patients, during relapse and remission. Moreover, plasma EV-EAAT2 levels correlated positively with Expanded Disability Status Scale (EDSS) score in remitting MS patients but showed a negative correlation with age in patients with secondary progressive (SPMS).

Conclusion: Our results emphaticize the usefulness of plasma EVs as a source of accessible biomarkers to remotely analyse the CNS status. Plasma EV-EAAT2 showed to be a promising biomarker for MS relapses. Further studies are required to assess the clinical relevance of this biomarker also for disability progression independent of relapse activity and transition from RRMS towards SPMS.

多发性硬化症患者血浆和脑脊液细胞外囊泡的蛋白质组图谱揭示了与疾病活动相关的 EAAT2。
背景和目的:目前迫切需要发现基于血液的多发性硬化症(MS)生物标志物,以更好地确定复发的潜在生物学特性并监测疾病进展。本研究的主要目的是寻找与循环细胞外囊泡(EVs)相关的多发性硬化复发候选生物标志物,EVs是一种新兴的生物标志物发现工具:通过大小排阻色谱法(SEC)从RRMS患者未配对的血浆和脑脊液样本中纯化出的EVs进行了蛋白质组学分析,以发现与多发性硬化症复发相关的新型生物标记物。通过比较与复发相关的血浆和脑脊液-EV蛋白质组,发现了疾病活动的候选生物标志物。结果发现,血浆-脑脊液-EV蛋白质组和血浆-脑脊液-EV蛋白质组的蛋白质图谱均与多发性硬化症复发相关:SEC纯化的血浆EVs(来自6名复发患者和5名缓解患者)和SEC纯化的脑脊液EVs(来自4名复发患者和3名缓解患者)的蛋白质组图谱显示,一组与多发性硬化症复发有关的蛋白质在突触传递通路中显著富集。在常见的蛋白质中,兴奋性氨基酸转运体2(EAAT2)负责中枢神经系统的大部分谷氨酸摄取,值得进一步研究。通过筛查 110 名多发性硬化症患者的血浆样本,我们发现血浆中携带的 EV-EAAT2 蛋白(EV-EAAT2)与多发性硬化症复发有显著关联,与疾病调节疗法无关。通过对 10 名 RRMS 患者在复发和缓解期间纵向采集的血浆样本中 EV-EAAT2 的存在进行调查,证实了这一发现。此外,缓解期多发性硬化症患者血浆中的EV-EAAT2水平与扩展残疾状态量表(EDSS)评分呈正相关,但在继发性进展期(SPMS)患者中,EV-EAAT2水平与年龄呈负相关:我们的研究结果强调了血浆EV作为可获取的生物标志物来源对远程分析中枢神经系统状况的有用性。血浆中的EV-EAAT2是一种很有前景的多发性硬化症复发生物标志物。还需要进一步的研究来评估该生物标志物对独立于复发活动的残疾进展以及从 RRMS 向 SPMS 过渡的临床意义。
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来源期刊
Journal of Neuroinflammation
Journal of Neuroinflammation 医学-神经科学
CiteScore
15.90
自引率
3.20%
发文量
276
审稿时长
1 months
期刊介绍: The Journal of Neuroinflammation is a peer-reviewed, open access publication that emphasizes the interaction between the immune system, particularly the innate immune system, and the nervous system. It covers various aspects, including the involvement of CNS immune mediators like microglia and astrocytes, the cytokines and chemokines they produce, and the influence of peripheral neuro-immune interactions, T cells, monocytes, complement proteins, acute phase proteins, oxidative injury, and related molecular processes. Neuroinflammation is a rapidly expanding field that has significantly enhanced our knowledge of chronic neurological diseases. It attracts researchers from diverse disciplines such as pathology, biochemistry, molecular biology, genetics, clinical medicine, and epidemiology. Substantial contributions to this field have been made through studies involving populations, patients, postmortem tissues, animal models, and in vitro systems. The Journal of Neuroinflammation consolidates research that centers around common pathogenic processes. It serves as a platform for integrative reviews and commentaries in this field.
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