| Literature DB >> 30667370 |
Silvia Pozzi1, Sai Sampath Thammisetty1, Philippe Codron1,2, Reza Rahimian1, Karine Valérie Plourde1, Geneviève Soucy1, Christine Bareil1, Daniel Phaneuf1, Jasna Kriz1,3, Claude Gravel1,3, Jean-Pierre Julien1,3.
Abstract
The cytoplasmic aggregation of TAR DNA-binding protein-43 (TDP-43) is a hallmark of degenerating neurons in amyotrophic lateral sclerosis (ALS) and subsets of frontotemporal dementia (FTD). In order to reduce TDP-43 pathology, we generated single-chain (scFv) antibodies against the RNA recognition motif 1 (RRM1) of TDP-43, which is involved in abnormal protein self-aggregation and interaction with p65 NF-κB. Virus-mediated delivery into the nervous system of a scFv antibody, named VH7Vk9, reduced microgliosis in a mouse model of acute neuroinflammation and mitigated cognitive impairment, motor defects, TDP-43 proteinopathy, and neuroinflammation in transgenic mice expressing ALS-linked TDP-43 mutations. These results suggest that antibodies targeting the RRM1 domain of TDP-43 might provide new therapeutic avenues for the treatment of ALS and FTD.Entities:
Keywords: Immunotherapy; Neurological disorders; Neuroscience; Therapeutics
Year: 2019 PMID: 30667370 PMCID: PMC6436898 DOI: 10.1172/JCI123931
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808