A high-content neuron imaging assay demonstrates inhibition of prion disease-associated neurotoxicity by an anti-prion protein antibody

• Published in: Scientific reports 2022-06, Vol.12 (1), p.9493-12, Article 9493
• Main Authors: Reilly, Madeleine, Benilova, Iryna, Khalili-Shirazi, Azadeh, Schmidt, Christian, Ahmed, Parvin, Yip, Daniel, Jat, Parmjit S., Collinge, John
• Format: Article
• Language: English
• Subjects: 631/80; 631/80/2373; 631/80/470/460; Alzheimer's disease; Animal models; Animals; Drug development; Global health; Humanities and Social Sciences; Mice; Monoclonal antibodies; multidisciplinary; Neurodegenerative diseases; Neurons - metabolism; Neurotoxicity; Neurotoxicity Syndromes - metabolism; Prion Diseases - metabolism; Prion protein; Prion Proteins - metabolism; Prions - metabolism; Propagation; Protein folding; Proteins; Science; Science (multidisciplinary)
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-022-13455-z

There is an urgent need to develop disease-modifying therapies to treat neurodegenerative diseases which pose increasing challenges to global healthcare systems. Prion diseases, although rare, provide a paradigm to study neurodegenerative dementias as similar disease mechanisms involving propagation and spread of multichain assemblies of misfolded protein (“prion-like” mechanisms) are increasingly recognised in the commoner conditions such as Alzheimer’s disease. However, studies of prion disease pathogenesis in mouse models showed that prion propagation and neurotoxicity can be mechanistically uncoupled and in vitro assays confirmed that highly purified prions are indeed not directly neurotoxic. To aid development of prion disease therapeutics we have therefore developed a cell-based assay for the specific neurotoxicity seen in prion diseases rather than to simply assess inhibition of prion propagation. We applied this assay to examine an anti-prion protein mouse monoclonal antibody (ICSM18) known to potently cure prion-infected cells and to delay onset of prion disease in prion-infected mice. We demonstrate that whilst ICSM18 itself lacks inherent neurotoxicity in this assay, it potently blocks prion disease-associated neurotoxicity.