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  • Long-term correction of Sandhoff disease following intravenous delivery of rAAV9 to mouse neonates.

Long-term correction of Sandhoff disease following intravenous delivery of rAAV9 to mouse neonates.

Molecular therapy : the journal of the American Society of Gene Therapy (2014-12-18)
Jagdeep S Walia, Naderah Altaleb, Alexander Bello, Christa Kruck, Matthew C LaFave, Gaurav K Varshney, Shawn M Burgess, Biswajit Chowdhury, David Hurlbut, Richard Hemming, Gary P Kobinger, Barbara Triggs-Raine
ABSTRACT

G(M2) gangliosidoses are severe neurodegenerative disorders resulting from a deficiency in β-hexosaminidase A activity and lacking effective therapies. Using a Sandhoff disease (SD) mouse model (Hexb(-/-)) of the G(M2) gangliosidoses, we tested the potential of systemically delivered adeno-associated virus 9 (AAV9) expressing Hexb cDNA to correct the neurological phenotype. Neonatal or adult SD and normal mice were intravenously injected with AAV9-HexB or -LacZ and monitored for serum β-hexosaminidase activity, motor function, and survival. Brain G(M2) ganglioside, β-hexosaminidase activity, and inflammation were assessed at experimental week 43, or an earlier humane end point. SD mice injected with AAV9-LacZ died by 17 weeks of age, whereas all neonatal AAV9-HexB-treated SD mice survived until 43 weeks (P < 0.0001) with only three exhibiting neurological dysfunction. SD mice treated as adults with AAV9-HexB died between 17 and 35 weeks. Neonatal SD-HexB-treated mice had a significant increase in brain β-hexosaminidase activity, and a reduction in G(M2) ganglioside storage and neuroinflammation compared to adult SD-HexB- and SD-LacZ-treated groups. However, at 43 weeks, 8 of 10 neonatal-HexB injected control and SD mice exhibited liver or lung tumors. This study demonstrates the potential for long-term correction of SD and other G(M2) gangliosidoses through early rAAV9 based systemic gene therapy.

MATERIALS
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Brand
Product Description

Methanol, purification grade, 99.8%
Chloroform, contains amylenes as stabilizer, ACS reagent, ≥99.8%
Chloroform, analytical standard
Chloroform, anhydrous, ≥99%, contains 0.5-1.0% ethanol as stabilizer
Chloroform, ACS spectrophotometric grade, ≥99.8%, contains 0.5-1.0% ethanol as stabilizer
Chloroform, contains ethanol as stabilizer, ACS reagent, ≥99.8%
Chloroform, Pharmaceutical Secondary Standard; Certified Reference Material
Chloroform, anhydrous, contains amylenes as stabilizer, ≥99%
Chloroform, ≥99%, PCR Reagent, contains amylenes as stabilizer
Chloroform, contains 100-200 ppm amylenes as stabilizer, ≥99.5%
Methanol, ACS spectrophotometric grade, ≥99.9%
Methanol, ACS reagent, ≥99.8%
Methanol, ACS reagent, ≥99.8%
Methanol, analytical standard
Methanol, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥99.8% (GC)
Methanol, anhydrous, 99.8%
Methanol, puriss., meets analytical specification of Ph Eur, ≥99.7% (GC)
Methanol, BioReagent, ≥99.93%
Methanol, suitable for HPLC, ≥99.9%
Methanol, HPLC Plus, ≥99.9%
Methanol, Laboratory Reagent, ≥99.6%
Methanol, suitable for HPLC, gradient grade, ≥99.9%
Methanol, suitable for HPLC, gradient grade, suitable as ACS-grade LC reagent, ≥99.9%
Methanol, Pharmaceutical Secondary Standard; Certified Reference Material
Methanol, ACS reagent, ≥99.8%
Methanol solution, contains 0.50 % (v/v) triethylamine
3,3′-Diaminobenzidine, 97% (HPLC)
Sigma-Aldrich
3,3′-Diaminobenzidine, 97%
USP
Methyl alcohol, United States Pharmacopeia (USP) Reference Standard
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