Small extracellular vesicles as emerging biomarkers and therapeutic targets in neurodegenerative diseases

IF 4.1 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Clinica Chimica Acta Pub Date : 2026-05-15 Epub Date: 2026-02-26 DOI:10.1016/j.cca.2026.120932
Askarova Zebo Zafarjonovna , Elmuratova Aysulu , Sanoeva Matlyuba , Hamroyev Rashid , Jurakulov Bakhrom Azamatovich , Ahmadjonov Ahmadjon , Amirullayeva Barno , Azimova Mayram Kurbanovna , Mahsudali Rohataliyev Mahmudali ugli , Iskandarova Shaxodat , Turakulov Rustam , Matrizaeva Gulnara Jumaniyazovna , Alisher Ishankulov
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引用次数: 0

Abstract

Small extracellular vesicles (sEVs) have rapidly emerged as versatile mediators of intercellular communication with significant potential to transform the diagnosis and treatment of neurodegenerative diseases (NDDs). Increasing evidence shows that sEVs not only participate in the propagation of pathogenic proteins but also serve as accessible, CNS-informative carriers of molecular signatures that reflect neuronal, glial, and systemic disease processes. This dual role positions sEVs at the intersection of biomarker discovery and therapeutic innovation. In the diagnostic domain, advances in immunoaffinity capture, single-vesicle analysis, and multi-omics profiling have enabled increasingly precise characterization of neuron-, astrocyte-, and microglia-derived sEVs, revealing candidate markers for Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, and related disorders. However, translation remains limited by methodological heterogeneity, a lack of large-scale validation, and the need for standardized pre-analytical and analytical pipelines aligned with the ISEV/MISEV guidelines. On the therapeutic front, native and engineered sEVs, particularly those derived from mesenchymal and neural stem cells, demonstrate promising neuroprotective effects, including the modulation of neuroinflammation; the enhancement of synaptic resilience; and the delivery of antioxidant, anti-amyloid, or gene-modifying cargo across the blood–brain barrier. Scalable GMP manufacturing, cargo-loading strategies, targeting specificity, and long-term safety remain key challenges for clinical translation. This narrative review synthesizes current advances in sEV-based biomarkers and therapeutics, outlines technological and regulatory barriers, and proposes a translational roadmap spanning mechanistic discovery, platform standardization, and integration into precision-medicine frameworks. Collectively, emerging data position sEVs as powerful tools capable of reshaping the diagnostic and therapeutic landscape of NDDs, provided that coordinated multidisciplinary efforts address the remaining gaps in validation, scalability, and regulatory readiness.
细胞外小泡作为神经退行性疾病的新兴生物标志物和治疗靶点。
小细胞外囊泡(sev)已迅速成为细胞间通讯的多功能介质,具有改变神经退行性疾病(ndd)诊断和治疗的巨大潜力。越来越多的证据表明,sev不仅参与致病性蛋白的繁殖,而且作为反映神经元、胶质和全身性疾病过程的分子特征的可接近的、具有中枢神经系统信息的载体。这种双重作用使sev处于生物标志物发现和治疗创新的交叉点。在诊断领域,免疫亲和力捕获、单囊泡分析和多组学分析的进步使得神经元、星形胶质细胞和小胶质细胞衍生的sev的特征越来越精确,揭示了阿尔茨海默病、帕金森病、肌萎缩侧索硬化症和相关疾病的候选标记物。然而,翻译仍然受到方法异质性、缺乏大规模验证以及需要与ISEV/MISEV指南一致的标准化分析前和分析管道的限制。在治疗方面,天然和工程sev,特别是来自间充质和神经干细胞的sev,显示出有希望的神经保护作用,包括调节神经炎症;突触弹性的增强;以及通过血脑屏障运送抗氧化剂、抗淀粉样蛋白或基因修饰的货物。可扩展的GMP生产、装载策略、靶向特异性和长期安全性仍然是临床转化的关键挑战。本文综述了基于sev的生物标志物和治疗方法的最新进展,概述了技术和监管障碍,并提出了一个跨越机制发现、平台标准化和整合到精准医学框架的转化路线图。总的来说,新兴数据将sev定位为能够重塑ndd诊断和治疗格局的强大工具,前提是协调多学科努力解决验证、可扩展性和监管准备方面的剩余差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinica Chimica Acta
Clinica Chimica Acta 医学-医学实验技术
CiteScore
10.10
自引率
2.00%
发文量
1268
审稿时长
23 days
期刊介绍: The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells. The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.
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