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增强中枢神经系统中的抗体暴露:摄取和清除机制以及改善脑内递送的策略

Enhancing Antibody Exposure in the Central Nervous System: Mechanisms of Uptake, Clearance, and Strategies for Improved Brain Delivery.

作者信息

Schwinghamer Kelly, Siahaan Teruna J

机构信息

Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, KS 66046, USA.

出版信息

J Nanotheranostics. 2023 Dec;4(4):463-479. doi: 10.3390/jnt4040020. Epub 2023 Oct 2.


DOI:10.3390/jnt4040020
PMID:39897432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11784990/
Abstract

Antibodies (mAbs) are attractive molecules for their application as a diagnostic and therapeutic agent for diseases of the central nervous system (CNS). mAbs can be generated to have high affinity and specificity to target molecules in the CNS. Unfortunately, only a very small number of mAbs have been specifically developed and approved for neurological indications. This is primarily attributed to their low exposure within the CNS, hindering their ability to reach and effectively engage their potential targets in the brain. This review discusses aspects of various barriers such as the blood-brain barrier (BBB) and blood-cerebrospinal fluid (CSF) barrier (BCSFB) that regulate the entry and clearance of mAbs into and from the brain. The roles of the glymphatic system on brain exposure and clearance are being described. We also discuss the proposed mechanisms of the uptake of mAbs into the brain and for clearance. Finally, several methods of enhancing the exposure of mAbs in the CNS were discussed, including receptor-mediated transcytosis, osmotic BBB opening, focused ultrasound (FUS), BBB-modulating peptides, and enhancement of mAb brain retention.

摘要

抗体(单克隆抗体)作为中枢神经系统(CNS)疾病的诊断和治疗剂具有很大的应用潜力。单克隆抗体可以被制备成对中枢神经系统中的靶分子具有高亲和力和特异性。不幸的是,只有极少数单克隆抗体被专门开发并批准用于神经学适应症。这主要归因于它们在中枢神经系统中的低暴露率,阻碍了它们到达并有效作用于大脑中潜在靶点的能力。本综述讨论了各种屏障的相关方面,如血脑屏障(BBB)和血脑脊液屏障(BCSFB),它们调节单克隆抗体进入和离开大脑的过程。文中描述了类淋巴系统在大脑暴露和清除方面的作用。我们还讨论了单克隆抗体进入大脑和清除的推测机制。最后,讨论了几种增强单克隆抗体在中枢神经系统中暴露的方法,包括受体介导的转胞吞作用、渗透性血脑屏障开放、聚焦超声(FUS)、血脑屏障调节肽以及增强单克隆抗体在大脑中的滞留。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed2/11784990/d72515646f20/nihms-2011983-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed2/11784990/d72515646f20/nihms-2011983-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed2/11784990/d72515646f20/nihms-2011983-f0001.jpg

相似文献

[1]
Enhancing Antibody Exposure in the Central Nervous System: Mechanisms of Uptake, Clearance, and Strategies for Improved Brain Delivery.

J Nanotheranostics. 2023-12

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
The glymphatic system: a new perspective on brain diseases.

Front Aging Neurosci. 2023-6-15

[2]
Anti-Amyloid Monoclonal Antibodies are Transformative Treatments that Redefine Alzheimer's Disease Therapeutics.

Drugs. 2023-5

[3]
Loss of aquaporin-4 results in glymphatic system dysfunction via brain-wide interstitial fluid stagnation.

Elife. 2023-2-9

[4]
Moving the Needle on Alzheimer's Disease with an Anti-Oligomer Antibody.

N Engl J Med. 2023-1-5

[5]
Investigating brain uptake of a non-targeting monoclonal antibody after intravenous and intracerebroventricular administration.

Front Pharmacol. 2022-8-29

[6]
A Historical Review of Brain Drug Delivery.

Pharmaceutics. 2022-6-16

[7]
Amyloid-Related Imaging Abnormalities With Anti-amyloid Antibodies for the Treatment of Dementia Due to Alzheimer's Disease.

Front Neurol. 2022-3-23

[8]
Sub-millimetre precision of drug delivery in the brain from ultrasound-triggered nanodroplets.

J Control Release. 2021-10-10

[9]
Evolution of blood-brain barrier in brain diseases and related systemic nanoscale brain-targeting drug delivery strategies.

Acta Pharm Sin B. 2021-8

[10]
Nanotherapeutics for Alzheimer's Disease with Preclinical Evaluation and Clinical Trials: Challenges, Promises and Limitations.

Curr Drug Deliv. 2022

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