Abstract:Phase III clinical trials of immunotherapies against Alzheimer’s disease have failed to hit major endpoints. Despite the high doses administered, small fractions of injected monoclonal antibodies cross the blood brain barrier (BBB), likely resulting in an antibody concentration in the brain parenchyma that is too low for a therapeutic effect. Here we report a novel approach to circumvent this obstacle. Leveraging the homing properties of endothelial progenitor cells (EPCs) to reach impaired BBB, we transfected… Show more
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