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通过mRNA表达的抗体-转铁蛋白偶联物经转胞吞作用驱动治疗神经退行性疾病

Transcytosis-Driven Treatment of Neurodegenerative Disorders by mRNA-Expressed Antibody-Transferrin Conjugates.

作者信息

Niazi Sarfaraz K, Magoola Matthias

机构信息

College of Pharmacy, University of Illinois, Chicago, IL 60612, USA.

DEI Biopharma, Kampala P.O. Box 35854, Uganda.

出版信息

Biomedicines. 2024 Apr 12;12(4):851. doi: 10.3390/biomedicines12040851.

Abstract

The recent setbacks in the withdrawal and approval delays of antibody treatments of neurodegenerative disorders (NDs), attributed to their poor entry across the blood-brain barrier (BBB), emphasize the need to bring novel approaches to enhance the entry across the BBB. One such approach is conjugating the antibodies that bind brain proteins responsible for NDs with the transferrin molecule. This glycoprotein transports iron into cells, connecting with the transferrin receptors (TfRs), piggybacking an antibody-transferrin complex that can subsequently release the antibody in the brain or stay connected while letting the antibody bind. This process increases the concentration of antibodies in the brain, enhancing therapeutic efficacy with targeted delivery and minimum systemic side effects. Currently, this approach is experimented with using drug-transferring conjugates assembled in vitro. Still, a more efficient and safer alternative is to express the conjugate using mRNA technology, as detailed in this paper. This approach will expedite safer discoveries that can be made available at a much lower cost than the recombinant process with in vitro conjugation. Most importantly, the recommendations made in this paper may save the antibodies against the NDs that seem to be failing despite their regulatory approvals.

摘要

神经退行性疾病(NDs)抗体治疗在撤药和审批延迟方面最近遭遇挫折,原因是其穿越血脑屏障(BBB)的能力较差,这凸显了采用新方法增强穿越血脑屏障能力的必要性。一种这样的方法是将与导致神经退行性疾病的脑蛋白结合的抗体与转铁蛋白分子结合。这种糖蛋白将铁转运到细胞中,与转铁蛋白受体(TfRs)结合,搭载抗体 - 转铁蛋白复合物,该复合物随后可在大脑中释放抗体或在抗体结合时保持连接状态。这一过程会增加大脑中抗体的浓度,通过靶向递送提高治疗效果并使全身副作用最小化。目前,这种方法正在使用体外组装的药物 - 转铁蛋白缀合物进行试验。不过,一种更高效、更安全的替代方法是使用mRNA技术表达缀合物,本文将对此进行详细阐述。这种方法将加快更安全的发现,且能以比体外缀合的重组过程低得多的成本实现。最重要的是,本文提出的建议可能挽救那些尽管已获得监管批准但似乎仍失败的针对神经退行性疾病的抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6108/11048317/c8128c93a81f/biomedicines-12-00851-g001.jpg

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