Combination brain and systemic injections of AAV provide maximal functional and survival benefits in the Niemann-Pick mouse

Marco A. Passini, Jie Bu, Jonathan A. Fidler, Robin J. Ziegler, Joseph W. Foley, James C. Dodge, Wendy W. Yang, Jennifer Clarke, Tatyana V. Taksir, Denise A. Griffiths, Michael A. Zhao, Catherine R. O'Riordan, Edward H. Schuchman, Lamya S. Shihabuddin, Seng H. Cheng

Research output: Contribution to journalArticlepeer-review

62 Scopus citations

Abstract

Niemann-Pick disease (NPD) is caused by the loss of acid sphingomyelinase (ASM) activity, which results in widespread accumulation of undegraded lipids in cells of the viscera and CNS. In this study, we tested the effect of combination brain and systemic injections of recombinant adeno-associated viral vectors encoding human ASM (hASM) in a mouse model of NPD. Animals treated by combination therapy exhibited high levels of hASM in the viscera and brain, which resulted in near-complete correction of storage throughout the body. This global reversal of pathology translated to normal weight gain and superior recovery of motor and cognitive functions compared to animals treated by either brain or systemic injection alone. Furthermore, animals in the combination group did not generate antibodies to hASM, demonstrating the first application of systemic-mediated tolerization to improve the efficacy of brain injections. All of the animals treated by combination therapy survived in good health to an investigator-selected 54 weeks, whereas the median lifespans of the systemic-alone, brain-alone, or untreated ASM knockout groups were 47, 48, and 34 weeks, respectively. These data demonstrate that combination therapy is a promising therapeutic modality for treating NPD and suggest a potential strategy for treating disease indications that cause both visceral and CNS pathologies.

Original languageEnglish
Pages (from-to)9505-9510
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume104
Issue number22
DOIs
StatePublished - 29 May 2007

Keywords

  • Acid sphingomyelinase
  • Adeno-associated virus
  • Immunotolerization
  • Lysosomal storage disease
  • Neurodegeneraton

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