Intravenous administration of scAAV9-Hexb normalizes lifespan and prevents pathology in Sandhoff disease mice
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Authors
N. Niemer, L. Rouviere, A. Besse, M.T. Vanier, J. Dmytrus, T. Marais, S. Astord, J-P. Puech, G. Panasyuk, J.D. Cooper, M. Barkats, C. Caillaud


Lab
Institut Necker-Enfants Malades, Paris, France

Journal
Human Molecular Genetics

Abstract
Sandhoff disease (SD) is a rare inherited disorder caused by a deficiency of β-hexosaminidase activity which is fatal because no effective treatment is available. A mouse model of Hexb deficiency reproduces the key pathognomonic features of SD patients with severe ubiquitous lysosomal dysfunction, GM2 accumulation, neuroinflammation and neurodegeneration, culminating in death at 4 months. Here, we show that a single intravenous neonatal administration of a self-complementary adeno-associated virus 9 vector (scAAV9) expressing the Hexb cDNA in SD mice is safe and sufficient to prevent disease development. Importantly, we demonstrate for the first time that this treatment results in a normal lifespan (over 700 days) and normalizes motor function assessed by a battery of behavioral tests, with scAAV9-treated SD mice being indistinguishable from wild-type littermates. Biochemical analyses in multiple tissues showed a significant increase in hexosaminidase A activity, which reached 10-15% of normal levels. AAV9 treatment was sufficient to prevent GM2 and GA2 storage almost completely in cerebrum (less so in cerebellum), as well as thalamic reactive gliosis and thalamocortical neuron loss in treated Hexb-/- mice. In summary, this study demonstrated a widespread protective effect throughout the entire CNS after a single intravenous administration of scAAV9-Hexb vector to neonatal SD mice.

BIOSEB Instruments Used:
Aron Test or Four Plates Test (LE830),Activmeter (BIO-ACTIV-R),Rotarod (BX-ROD)

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