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鞘内免疫选择性纳滤治疗阿尔茨海默病:是什么,如何进行?为什么,何时进行?

Intrathecal Immunoselective Nanopheresis for Alzheimer's Disease: What and How? Why and When?

机构信息

Departamento de Medicina, Facultad de Ciencias de la Salud, Universidad de Oviedo, ES-33006 Oviedo, Spain.

Hospital Universitario Central de Asturias, Servicio de Neurología, ES-33011 Oviedo, Spain.

出版信息

Int J Mol Sci. 2024 Oct 2;25(19):10632. doi: 10.3390/ijms251910632.

DOI:10.3390/ijms251910632
PMID:39408961
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11476806/
Abstract

Nanotechnology is transforming therapeutics for brain disorders, especially in developing drug delivery systems. Intrathecal immunoselective nanopheresis with soluble monoclonal antibodies represents an innovative approach in the realm of drug delivery systems for Central Nervous System conditions, especially for targeting soluble beta-amyloid in Alzheimer's disease. This review delves into the concept of intrathecal immunoselective nanopheresis. It provides an overall description of devices to perform this technique while discussing the nanotechnology behind its mechanism of action, its potential advantages, and clinical implications. By exploring current research and advancements, we aim to provide a comprehensive understanding of this novel method, addressing the critical questions of what it is, how it works, why it is needed, and when it should be applied. Special attention is given to patient selection and the optimal timing for therapy initiation in Alzheimer's, coinciding with the peak accumulation of amyloid oligomers in the early stages. Potential limitations and alternative targets beyond beta-amyloid and future perspectives for immunoselective nanopheresis are also described.

摘要

纳米技术正在改变脑部疾病的治疗方法,特别是在开发药物输送系统方面。鞘内免疫选择纳米过滤与可溶性单克隆抗体代表了中枢神经系统疾病药物输送系统领域的一种创新方法,特别是针对阿尔茨海默病中可溶性β-淀粉样蛋白的靶向治疗。本综述深入探讨了鞘内免疫选择纳米过滤的概念。它全面描述了用于执行该技术的设备,同时讨论了其作用机制背后的纳米技术、潜在的优势以及临床意义。通过探索当前的研究和进展,我们旨在全面了解这种新方法,回答关于它是什么、如何工作、为什么需要以及何时应用的关键问题。特别关注阿尔茨海默病患者的选择和治疗开始的最佳时机,这与早期淀粉样寡聚体的峰值积累相吻合。还描述了免疫选择纳米过滤的潜在局限性和除β-淀粉样蛋白以外的替代靶点以及未来的展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6758/11476806/3a3d50b7da4d/ijms-25-10632-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6758/11476806/027a351ea6ec/ijms-25-10632-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6758/11476806/475c0f30a604/ijms-25-10632-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6758/11476806/3a3d50b7da4d/ijms-25-10632-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6758/11476806/027a351ea6ec/ijms-25-10632-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6758/11476806/475c0f30a604/ijms-25-10632-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6758/11476806/3a3d50b7da4d/ijms-25-10632-g003.jpg

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The dopaminergic system promotes neprilysin-mediated degradation of amyloid-β in the brain.多巴胺能系统促进脑内神经肽酶介导的淀粉样蛋白-β降解。
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Aβ oligomers peak in early stages of Alzheimer's disease preceding tau pathology.在阿尔茨海默病的早期阶段,β淀粉样蛋白寡聚体在tau蛋白病变之前达到峰值。
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