School of Pharmacy, The University of Queensland, Brisbane, QLD, 4102, Australia.
Translational Extracellular Vesicles in Obstetrics and Gynae-Oncology Group, The University of Queensland Centre for Clinical Research, Royal Brisbane and Women's Hospital, Faculty of Medicine, The University of Queensland, Brisbane, QLD, 4029, Australia.
Adv Healthc Mater. 2023 Nov;12(28):e2301010. doi: 10.1002/adhm.202301010. Epub 2023 Jul 8.
Extracellular vesicles (EVs) occur in a variety of bodily fluids and have gained recent attraction as natural materials due to their bioactive surfaces, internal cargo, and role in intercellular communication. EVs contain various biomolecules, including surface and cytoplasmic proteins; and nucleic acids that are often representative of the originating cells. EVs can transfer content to other cells, a process that is thought to be important for several biological processes, including immune responses, oncogenesis, and angiogenesis. An increased understanding of the underlying mechanisms of EV biogenesis, composition, and function has led to an exponential increase in preclinical and clinical assessment of EVs for biomedical applications, such as diagnostics and drug delivery. Bacterium-derived EV vaccines have been in clinical use for decades and a few EV-based diagnostic assays regulated under Clinical Laboratory Improvement Amendments have been approved for use in single laboratories. Though, EV-based products are yet to receive widespread clinical approval from national regulatory agencies such as the United States Food and Drug Administration (USFDA) and European Medicine Agency (EMA), many are in late-stage clinical trials. This perspective sheds light on the unique characteristics of EVs, highlighting current clinical trends, emerging applications, challenges and future perspectives of EVs in clinical use.
细胞外囊泡(EVs)存在于多种体液中,由于其具有生物活性的表面、内部货物以及在细胞间通讯中的作用,最近作为天然材料受到了关注。EVs 包含各种生物分子,包括表面和细胞质蛋白;以及核酸,这些核酸通常是起源细胞的代表。EVs 可以将内容物转移到其他细胞,这一过程被认为对包括免疫反应、肿瘤发生和血管生成在内的几种生物学过程很重要。对 EV 生物发生、组成和功能的潜在机制的深入了解,导致了对 EV 在生物医学应用中的临床前和临床评估的呈指数级增长,例如诊断和药物输送。细菌衍生的 EV 疫苗已经在临床上使用了几十年,并且已经批准了一些基于 EV 的诊断检测方法在单个实验室中使用,这些方法受到临床实验室改进修正案的监管。尽管如此,基于 EV 的产品尚未获得美国食品和药物管理局(USFDA)和欧洲药品管理局(EMA)等国家监管机构的广泛临床批准,但许多产品都处于临床试验的后期阶段。本观点阐明了 EV 的独特特征,强调了当前的临床趋势、新兴应用、基于 EV 的临床应用的挑战和未来展望。
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