| Literature DB >> 27582220 |
Jeff Sevigny1, Ping Chiao1, Thierry Bussière1, Paul H Weinreb1, Leslie Williams1, Marcel Maier2, Robert Dunstan1, Stephen Salloway3, Tianle Chen1, Yan Ling1, John O'Gorman1, Fang Qian1, Mahin Arastu1, Mingwei Li1, Sowmya Chollate1, Melanie S Brennan1, Omar Quintero-Monzon1, Robert H Scannevin1, H Moore Arnold1, Thomas Engber1, Kenneth Rhodes1, James Ferrero1, Yaming Hang1, Alvydas Mikulskis1, Jan Grimm2, Christoph Hock2,4, Roger M Nitsch2,4, Alfred Sandrock1.
Abstract
Alzheimer's disease (AD) is characterized by deposition of amyloid-β (Aβ) plaques and neurofibrillary tangles in the brain, accompanied by synaptic dysfunction and neurodegeneration. Antibody-based immunotherapy against Aβ to trigger its clearance or mitigate its neurotoxicity has so far been unsuccessful. Here we report the generation of aducanumab, a human monoclonal antibody that selectively targets aggregated Aβ. In a transgenic mouse model of AD, aducanumab is shown to enter the brain, bind parenchymal Aβ, and reduce soluble and insoluble Aβ in a dose-dependent manner. In patients with prodromal or mild AD, one year of monthly intravenous infusions of aducanumab reduces brain Aβ in a dose- and time-dependent manner. This is accompanied by a slowing of clinical decline measured by Clinical Dementia Rating-Sum of Boxes and Mini Mental State Examination scores. The main safety and tolerability findings are amyloid-related imaging abnormalities. These results justify further development of aducanumab for the treatment of AD. Should the slowing of clinical decline be confirmed in ongoing phase 3 clinical trials, it would provide compelling support for the amyloid hypothesis.Entities:
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Year: 2016 PMID: 27582220 DOI: 10.1038/nature19323
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962