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Retrograde Viral Delivery of IGF-1 Prolongs Survival in a Mouse ALS Model
Brian K. Kaspar,1Jerònia Lladó,2*Nushin Sherkat,1Jeffrey D. Rothstein,2Fred H. Gage1
Amyotrophic lateral sclerosis (ALS) is a progressive, lethalneuromuscular disease that is associated with the degenerationof spinal and brainstem motor neurons, leading to atrophy oflimb, axial, and respiratory muscles. The cause of ALS is unknown,and there is no effective therapy. Neurotrophic factors arecandidates for therapeutic evaluation in ALS. Although chronicdelivery of molecules to the central nervous system has provendifficult, we recently discovered that adeno-associated viruscan be retrogradely transported efficiently from muscle to motorneurons of the spinal cord. We report that insulin-like growthfactor 1 prolongs life and delays disease progression, evenwhen delivered at the time of overt disease symptoms.
1 Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA. 2 Departments of Neurology and Neuroscience, Johns Hopkins University, 600 North Wolfe Street, Meyer 6-109, Baltimore, MD 21287, USA.
* Present address: Institut Universitari d'Investigacióen Ciències de la Salut (IUNICS), Hospital Son Dureta,C/Andrea Doria 55, Edifici D 1a planta, 07014 Palma, Illes Balears,Spain.
To whom correspondence should be addressed. E-mail: gage{at}salk.edu
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