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一种靶向转铁蛋白受体1的单域鲨鱼抗体将TrkB激动剂抗体递送至大脑,并在帕金森病小鼠模型中提供完全的神经保护作用。

A Single Domain Shark Antibody Targeting the Transferrin Receptor 1 Delivers a TrkB Agonist Antibody to the Brain and Provides Full Neuroprotection in a Mouse Model of Parkinson's Disease.

作者信息

Clarke Emily, Stocki Pawel, Sinclair Elizabeth H, Gauhar Aziz, Fletcher Edward J R, Krawczun-Rygmaczewska Alicja, Duty Susan, Walsh Frank S, Doherty Patrick, Rutkowski Julia Lynn

机构信息

King's College London, Institute of Psychiatry, Psychology and Neuroscience, Wolfson Centre for Age-Related Disease, Guy's Campus, London SE1 1UL, UK.

Ossianix, Inc., Gunnels Wood Rd., Stevenage SG1 2FX, UK.

出版信息

Pharmaceutics. 2022 Jun 24;14(7):1335. doi: 10.3390/pharmaceutics14071335.

Abstract

Single domain shark antibodies that bind to the transferrin receptor 1 (TfR1) on brain endothelial cells have been used to shuttle antibodies and other cargos across the blood brain barrier (BBB) to the brain. For these studies the TXB4 brain shuttle was fused to a TrkB neurotrophin receptor agonist antibody. The TXB4-TrkB fusion retained potent agonist activity at its cognate receptor and after systemic administration showed a 12-fold increase in brain levels over the unmodified antibody. Only the TXB4-TrkB antibody fusion was detected within the brain and localized to TrkB positive cells in the cortex and tyrosine hydroxylase (TH) positive dopaminergic neurons in the substantia nigra pars compacta (SNc), where it was associated with activated ERK1/2 signaling. When tested in the 6-hydroxydopamine (6-OHDA) mouse model of Parkinson's disease (PD), TXB4-TrkB, but not the unmodified antibody, completely prevented the 6-OHDA induced death of TH positive neurons in the SNc. In conclusion, the fusion of the TXB4 brain shuttle allows a TrkB agonist antibody to reach neuroprotective concentrations in the brain parenchyma following systemic administration.

摘要

与脑内皮细胞上的转铁蛋白受体1(TfR1)结合的单域鲨鱼抗体已被用于将抗体和其他货物穿过血脑屏障(BBB)转运至大脑。在这些研究中,TXB4脑穿梭载体与TrkB神经营养因子受体激动剂抗体融合。TXB4-TrkB融合体在其同源受体上保留了强大的激动剂活性,全身给药后,其在脑中的水平比未修饰的抗体增加了12倍。仅在脑内检测到TXB4-TrkB抗体融合体,其定位于皮质中的TrkB阳性细胞和黑质致密部(SNc)中的酪氨酸羟化酶(TH)阳性多巴胺能神经元,在那里它与激活的ERK1/2信号传导相关。当在帕金森病(PD)的6-羟基多巴胺(6-OHDA)小鼠模型中进行测试时,TXB4-TrkB,而不是未修饰的抗体,完全阻止了6-OHDA诱导的SNc中TH阳性神经元的死亡。总之,TXB4脑穿梭载体的融合使得TrkB激动剂抗体在全身给药后能够在脑实质中达到神经保护浓度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7387/9318160/d8ffd1b21150/pharmaceutics-14-01335-g001.jpg

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