Faculty of Pharmaceutical Sciences, Osaka University, Osaka, Japan.
College of Pharmaceutical Sciences, Ritsumeikan University, Kusatsu, Japan.
Ann N Y Acad Sci. 2022 Aug;1514(1):62-69. doi: 10.1111/nyas.14787. Epub 2022 May 4.
The blood-brain barrier is a major obstacle to the delivery of drugs to the central nervous system. In the blood-brain barrier, the spaces between adjacent brain microvascular endothelial cells are sealed by multiprotein complexes known as tight junctions. Among the many components of the tight junction, claudin-5 has received the most attention as a target for loosening the tight-junction seal and allowing drugs to be delivered to the brain. In mice, transient knockdown of claudin-5 and the use of claudin-5 binders have been shown to enhance the permeation of small molecules from the blood into the brain without apparent adverse effects. However, sustained knockdown of claudin-5 in mice is lethal within 40 days, and administration of an anti-claudin-5 antibody induced convulsions in a nonhuman primate. Here, we review the safety concerns of claudin-5-targeted technologies with respect to their clinical application.
血脑屏障是药物向中枢神经系统递送的主要障碍。在血脑屏障中,相邻脑微血管内皮细胞之间的空间由称为紧密连接的多蛋白复合物封闭。在紧密连接的许多成分中,Claudin-5 作为一种松动紧密连接密封并允许药物递送到大脑的靶点受到了最多的关注。在小鼠中,Claudin-5 的瞬时敲低和 Claudin-5 结合物的使用已被证明可增强小分子从血液向大脑的渗透,而没有明显的不良反应。然而,在小鼠中持续敲低 Claudin-5 在 40 天内是致命的,并且抗 Claudin-5 抗体的给药在非人类灵长类动物中引起了惊厥。在这里,我们回顾了 Claudin-5 靶向技术在其临床应用中的安全性问题。