| Literature DB >> 22223800 |
Peter-Christian Klöhn1, Michael Farmer, Jacqueline M Linehan, Catherine O'Malley, Mar Fernandez de Marco, William Taylor, Mark Farrow, Azy Khalili-Shirazi, Sebastian Brandner, John Collinge.
Abstract
Intraperitoneal administration of ICSM18 and 35, monoclonal antibodies against prion protein (PrP), has been shown to significantly delay the onset of prion disease in mice, and humanized versions are candidate therapeutics for prion and Alzheimer's diseases. However, a previous report of severe and widespread apoptosis after intracerebral injection of anti-PrP monoclonal antibodies raised concerns about such therapy and led to an influential model of prion neurotoxicity via cross-linking of cell surface PrP by disease-related PrP aggregates. In extensive studies including ICSM18 and 35, fully humanized ICSM18, and the previously reported proapoptotic antibodies, we found no evidence of apoptosis, thereby questioning this model of prion neurotoxicity.Entities:
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Year: 2012 PMID: 22223800 DOI: 10.1126/science.1215579
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728