Why the study?
Targeting claudin-5 loosens the blood-brain barrier for drug delivery, but sustained knockdown or antibodies have caused severe adverse events, raising safety concerns for clinical application.
What are the safety concerns and risks associated with modifying the blood-brain barrier by targeting claudin-5?
What are the safety concerns and risks associated with modifying the blood-brain barrier by targeting claudin-5?
Targeting claudin-5 to open the blood-brain barrier carries significant safety risks, including lethality and convulsions, which must be addressed before clinical application.
Targeting claudin-5 may enable CNS drug delivery; leaves open clinical translation, safety, and efficacy in humans.
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.
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Wakayama et al. (2022) studied this question.
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