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Grant: Operating Grant - Priority Announcement: ALS Canada Research Fund

Université Laval

$0.00

Therapeutic nanobodies for amyotrophic lateral sclerosis

FY 2012-13

Summary
Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disorder characterized by the progressive degeneration of motor neurons. Here we propose to develop antibody-derived proteins (nanobodies) that will bind new therapeutic targets for ALS. The first part of the project aims to derive a nanobody-based therapy to reduce the burden of pathogenic misfolded superoxide dismutase proteins in the nervous system. We will compare the therapeutic effects of different methods for viral delivery of nanobodies in transgenic ALS mice overexpressing mutant SOD1. The second part aims to develop a nanobody-based therapy for TDP-43-mediated pathogenesis. TDP-43 aggregates are a hallmark of ALS and we recently proposed a pathogenic pathway based on the interaction of TDP-43 with the p65 subunit of nuclear factor kappa B, a key component of inflammatory responses. Viral vectors encoding nanobodies to block TDP-43 binding to p65 NF-kB will be tested in transgenic mice overexpressing mutant TDP-43 which develop pathological hallmarks of human ALS.
Program
Operating Grant - Priority Announcement: ALS Canada Research Fund
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
286585
Name
Julien Jean-Pierre
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Amyotrophic Lateral Sclerosis Society of Canada
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Molecular & Cellular Neurosciences - B
Projecttitle
Therapeutic nanobodies for amyotrophic lateral sclerosis
Programtype2
Operating Grants
Orgnameinp2
Université Laval
Cihramount2
$0
Cihrequipment2
$0
Programname2
Operating Grant - Priority Announcement: ALS Canada Research Fund
Keyworddelim
Amyotrophic Lateral Sclerosis; Neurodegeneration; Neuroinflammation; Superoxide Dismutase; Tdp-43; Transgenic Mice
Abstract
Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disorder characterized by the progressive degeneration of motor neurons. Here we propose to develop antibody-derived proteins (nanobodies) that will bind new therapeutic targets for ALS. The first part of the project aims to derive a nanobody-based therapy to reduce the burden of pathogenic misfolded superoxide dismutase proteins in the nervous system. We will compare the therapeutic effects of different methods for viral delivery of nanobodies in transgenic ALS mice overexpressing mutant SOD1. The second part aims to develop a nanobody-based therapy for TDP-43-mediated pathogenesis. TDP-43 aggregates are a hallmark of ALS and we recently proposed a pathogenic pathway based on the interaction of TDP-43 with the p65 subunit of nuclear factor kappa B, a key component of inflammatory responses. Viral vectors encoding nanobodies to block TDP-43 binding to p65 NF-kB will be tested in transgenic mice overexpressing mutant TDP-43 which develop pathological hallmarks of human ALS.
Competitiondate
201303
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Julien, Jean-Pierre
Approvedterm
2 ans 0 mois
Université Laval - $0 Grant (2012-13) | Canada Spends