A comparative study of the effects of Aducanumab and scanning ultrasound on amyloid plaques and behavior in the APP23 mouse model of Alzheimer disease.
Authors: Leinenga G, Koh WK, Götz J
Aducanumab is an anti-amyloid-β (Aβ) antibody that achieved reduced amyloid pathology in Alzheimer's disease (AD) trials; however, it is controversial whether it also improved cognition, which has been suggested would require a sufficiently high cumulative dose of the antibody in the brain. Therapeutic ultrasound, in contrast, has only begun to be investigated in human AD clinical trials. We have previously shown that scanning ultrasound in combination with intravenously injected microbubbles (SUS), which temporarily and safely opens the blood-brain barrier (BBB), removes amyloid and restores cognition in APP23 mice. However, there has been no direct testing of how the effects of SUS compare to immunotherapy or whether a combination therapy is more effective. In a study comprising four treatment arms, we tested the efficacy of an Aducanumab analog, Adu, both in comparison to SUS, and as a combination therapy, in APP23 mice (aged 13-22 months), using sham as a control. The active place avoidance (APA) test was used to test spatial memory, and histology and ELISA were used to measure amyloid. Brain antibody levels were also determined. We found that both Adu and SUS reduced the total plaque area in the hippocampus with no additive effect observed with the combination treatment (SUS + Adu). Whereas in the cortex where there was a trend towards reducing the total plaque area from either Adu or SUS, only the combination treatment yielded a statistically significant decrease in total plaque area compared to sham. Only the SUS and SUS + Adu groups included animals that had their plaque load reduced to below 1% from above 10%. There was a robust improvement in spatial memory for the SUS + Adu group only, and in this group the level of Adu, when measured 3 days post-treatment, was 5-fold higher compared to those mice that received Adu on its own. Together, these findings suggest that SUS should be considered as a treatment option for AD. Alternatively, a combination trial using Aducanumab together with ultrasound to increase brain levels of the antibody may be warranted.
Introduction
Purpose
Drug delivery with BBB opening
Study Objective
To compare the efficacy of an Aducanumab analog, scanning ultrasound (SUS), and their combination versus sham in reducing amyloid pathology and improving cognition in APP23 Alzheimer’s disease mice.
Animal model / Human subject
Mouse (APP23 transgenic), 13–22 months old, sex None
Disease model
Alzheimer's disease
Targeted brain region(s)
Hippocampus
Cargo name and characteristics
Aducanumab analog (referred to as 'Adu'): a monoclonal anti-amyloid-β (Aβ) antibody (protein) that targets aggregated Aβ, used intravenously in APP23 mice to reduce amyloid plaque burden and assess effects on cognition; brain antibody levels were measured post‑treatment.
Route of administration
Intravenous (systemic injection of the Aducanumab analog and intravenously injected microbubbles; scanning ultrasound used to open the blood–brain barrier)
Outcomes and Safety
Summary of Outcomes
Combining scanning ultrasound (SUS) with an Aducanumab analog increased brain antibody levels (~5-fold), produced greater cortical amyloid plaque clearance than either treatment alone and uniquely improved spatial memory in APP23 mice, while SUS or Adu alone reduced hippocampal plaques without behavioral improvement.
Duration of biological effect
3 days
Safety-related matter
SUS is described as temporarily and safely opening the BBB; Adu (alone or with SUS) did not increase microhemorrhages or CAA in APP23 mice, although clinical trials reported microbleeds in <10% of patients and the safety of repeatedly opening large brain areas remains a concern.
Brain Region
Ultrasound Parameters
Ultrasound instrument
Scanning ultrasound (SUS); no instrument model or manufacturer specified; transducer aperture/diameter None.
FUS Mode
pulsed
Treatment frequency
multiple sessions
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