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Mechanism of amyloid removal in patients with Alzheimer disease treated with gantenerumab

Authors

Ostrowitzki, Susanne, Deptula, Dennis, Thurfjell, Lennart, Barkhof, Frederik, Bohrmann, Bernd, Brooks, David J., Klunk, William E., Ashford, Elizabeth, Yoo, Kisook, Xu, Zhi-Xin, Loetscher, Hansruedi, Santarelli, Luca

Journal

Archives Of Neurology, Volume: 69, No.: 2, Pages.: 198-207

Year of Publication

2012

Abstract

Background: Gantenerumab is a fully human anti-Aβ monoclonal antibody in clinical development for the treatment of Alzheimer disease (AD).; Objectives: To investigate whether treatment with gantenerumab leads to a measurable reduction in the level of Aβ amyloid in the brain and to elucidate the mechanism of amyloid reduction.; Design: A multicenter, randomized, double-blind, placebo-controlled, ascending-dose positron emission tomographic study. Additionally, ex vivo studies of human brain slices from an independent sample of patients who had AD were performed.; Setting: Three university medical centers.; Patients: Patients with mild-to-moderate AD.; Intervention: Two consecutive cohorts of patients received 2 to 7 infusions of intravenous gantenerumab (60 or 200 mg) or placebo every 4 weeks. Brain slices from patients who had AD were coincubated with gantenerumab at increasing concentrations and with human microglial cells.; Main Outcome Measures: Percent change in the ratio of regional carbon 11-labeled Pittsburgh Compound B retention in vivo and semiquantitative assessment of gantenerumab-induced phagocytosis ex vivo.; Results: Sixteen patients with end-of-treatment positron emission tomographic scans were included in the analysis. The mean (95% CI) percent change from baseline difference relative to placebo (n = 4) in cortical brain amyloid level was -15.6% (95% CI, -42.7 to 11.6) for the 60-mg group (n = 6) and -35.7% (95% CI, -63.5 to -7.9) for the 200-mg group (n = 6). Two patients in the 200-mg group showed transient and focal areas of inflammation or vasogenic edema on magnetic resonance imaging scans at sites with the highest level of amyloid reduction. Gantenerumab induced phagocytosis of human amyloid in a dose-dependent manner ex vivo.; Conclusion: Gantenerumab treatment resulted in a dose-dependent reduction in brain amyloid level, possibly through an effector cell-mediated mechanism of action.;

Bibtex Citation

@article{Ostrowitzki_2012, doi = {10.1001/archneurol.2011.1538}, url = {http://dx.doi.org/10.1001/archneurol.2011.1538}, year = 2012, month = {feb}, publisher = {American Medical Association ({AMA})}, volume = {69}, number = {2}, pages = {198}, author = {Susanne Ostrowitzki}, title = {Mechanism of Amyloid Removal in Patients With Alzheimer Disease Treated With Gantenerumab}, journal = {Arch Neurol} }

Keywords

aged, alzheimer disease, alzheimer vaccines, amyloid, amyloid betapeptides, aniline compounds, antibodies monoclonal, brain chemistry, cell count, cohort studies, diagnostic use, doubleblind method, drug effects, drug therapy, female, followup studies, gantenerumab, humans, immunoglobulin g, immunology, injections intravenous, levels, male, metabolism, microglia, middle aged, phagocytosis, physiology, positronemission tomography, radiopharmaceuticals, radiotherapy, sample size, therapeutic use, thiazoles

Countries of Study

Switzerland

Types of Dementia

Alzheimer’s Disease

Types of Study

Case Control Study

Type of Outcomes

Other

Type of Interventions

Pharmaceutical Interventions

Pharmaceutical Interventions

Other