Brain-penetrant complement inhibition mitigates neurodegeneration in an Alzheimer’s disease mouse model

Complement activation is implicated in driving brain inflammation, self-cell damage and progression of injury in Alzheimer's disease and other neurodegenerative diseases. Here, we investigate the impact of brain delivery of a complement-blocking antibody on neurodegeneration in an Alzheimer's mouse model. We engineered a brain-penetrant recombinant antibody targeting the pro-inflammatory membrane attack complex. Systemic administration of this antibody in APPNL-G-F mice reduced brain levels of complement activation products, demonstrating successful brain entry and target engagement. Prolonged treatment decreased synapse loss, amyloid burden and brain inflammatory cytokine levels, concomitant with cognitive improvement compared to controls. These results underscore the potential of brain-penetrant complement-inhibiting drugs as promising therapeutics, targeting downstream of amyloid plaques in Alzheimer's disease.

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Publication Details

Journal
Brain
Published
2024-08-31
DOI
https://doi.org/10.1093/brain/awae278
Citations
17
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
4.21

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article

Brain-penetrant complement inhibition mitigates neurodegeneration in an Alzheimer’s disease mouse model

Bart De Strooper, Ryan J. Bevan, Maarten Dewilde, Wioleta M. Zelek et al.
17 citations
Brain
Neuroinflammation and Neurodegeneration Mechanisms
4.21
article

Brain-penetrant complement inhibition mitigates neurodegeneration in an Alzheimer’s disease mouse model

Bart De Strooper, Ryan J. Bevan, Maarten Dewilde, Wioleta M. Zelek, Jacqui Nimmo, B. Paul Morgan
article en
17 citations

Abstract

Complement activation is implicated in driving brain inflammation, self-cell damage and progression of injury in Alzheimer's disease and other neurodegenerative diseases. Here, we investigate the impact of brain delivery of a complement-blocking antibody on neurodegeneration in an Alzheimer's mouse model. We engineered a brain-penetrant recombinant antibody targeting the pro-inflammatory membrane attack complex. Systemic administration of this antibody in APPNL-G-F mice reduced brain levels of complement activation products, demonstrating successful brain entry and target engagement. Prolonged treatment decreased synapse loss, amyloid burden and brain inflammatory cytokine levels, concomitant with cognitive improvement compared to controls. These results underscore the potential of brain-penetrant complement-inhibiting drugs as promising therapeutics, targeting downstream of amyloid plaques in Alzheimer's disease.

BrainVol. 148(3)
UK Dementia Research Institute (GB), Research & Diagnostic Antibodies (United States) (US), VIB-KU Leuven Center for Brain & Disease Research (BE), University College London (GB), Cardiff University (GB), KU Leuven (BE)
LifeArc, UK Research and Innovation, KU Leuven, Vlaams Instituut voor Biotechnologie, UK Dementia Research Institute, Medical Research Council
Good health and well-being
Openalex Percentile: Top 5%
Neuroinflammation and Neurodegeneration Mechanisms
4.21
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