Chatzopoulos Michail K, Fragoulis George E, Samiotaki Martina, Tektonidou Maria G, Sfikakis Petros P, Vetsika Eleni-Kyriaki
First Department of Propaedeutic Internal Medicine, Joint Rheumatology Program, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Institute for Bio-innovation, Biomedical Sciences Research Center "Alexander Fleming", Vari, 16672, Greece.
Rheumatol Int. 2025 Sep 1;45(9):211. doi: 10.1007/s00296-025-05953-w.
Increasing evidence has shown the role of small extracellular vesicles (sEVs) in autoimmune rheumatic diseases (ARDs). This systematic literature review aims to evaluate the role of sEVs as biomarkers in ARDs, focusing on their molecular cargo and their utility for disease diagnosis, monitoring, and treatment response. A systematic search was conducted in MEDLINE/PubMed and Scopus from inception until July 2025, using the search terms; [(small extracellular vesicles) or exosomes) and ((rheumatic disease) or (rheumatoid arthritis) or (psoriatic arthritis) or (axial spondylarthritis) or (ankylosing spondylitis) or (systemic lupus erythematosus) or (Sjögren's syndrome) or scleroderma or (systemic sclerosis) or myositis or polymyositis)]. Eligible studies were those reporting on sEV isolation from patient samples and comparing it with healthy individuals or controls with non-inflammatory conditions. The initial search yielded 1593 results, and 46 studies met the inclusion criteria. Literature reviews revealed that miRNAs and long non-coding (lnc)RNAs isolated from sEVs might serve as potential biomarkers for disease activity and treatment response in ARDs, mainly in rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). In addition, sEV miRNA-21 and miRNA-146a have been often described in studies in SLE patients, indicating their potential role in differentiating SLE from healthy individuals. Although proteomic studies identified disease-specific proteins within sEVs, there is no consensus among the limited studies reporting sEV proteins. Although numerous studies have examined the role of sEVs in ARDs, there is a lack of consensus in the findings. Further research using well-standardized methodologies is needed to ensure reliable and reproducible results. PROSPERO 2025 CRD420250646438. Available from https://www.crd.york.ac.uk/PROSPERO/view/CRD420250646438 .
越来越多的证据表明,细胞外小囊泡(sEVs)在自身免疫性风湿性疾病(ARDs)中发挥着作用。本系统文献综述旨在评估sEVs作为ARDs生物标志物的作用,重点关注其分子载荷及其在疾病诊断、监测和治疗反应方面的效用。从数据库建立至2025年7月,在MEDLINE/PubMed和Scopus中进行了系统检索,检索词为:[(细胞外小囊泡)或外泌体)以及((风湿性疾病)或(类风湿性关节炎)或(银屑病关节炎)或(轴性脊柱关节炎)或(强直性脊柱炎)或(系统性红斑狼疮)或(干燥综合征)或硬皮病或(系统性硬化症)或肌炎或多发性肌炎)]。符合条件的研究是那些报告从患者样本中分离sEVs并将其与健康个体或非炎症性疾病对照进行比较的研究。初步检索产生了1593条结果,46项研究符合纳入标准。文献综述显示,从sEVs中分离出的微小RNA(miRNAs)和长链非编码(lnc)RNAs可能作为ARDs疾病活动和治疗反应的潜在生物标志物,主要用于类风湿性关节炎(RA)和系统性红斑狼疮(SLE)。此外,sEV miRNA - 21和miRNA - 146a在SLE患者的研究中经常被提及,表明它们在区分SLE患者与健康个体方面的潜在作用。尽管蛋白质组学研究在sEVs中鉴定出了疾病特异性蛋白质,但在报告sEV蛋白质的有限研究中尚未达成共识。尽管众多研究探讨了sEVs在ARDs中的作用,但研究结果缺乏一致性。需要使用标准化方法进行进一步研究,以确保结果可靠且可重复。PROSPERO 2025 CRD420250646438。可从https://www.crd.york.ac.uk/PROSPERO/view/CRD420250646438获取。
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