Literature DB >> 17517638

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

Marco A Passini1, 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.   

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.

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Year:  2007        PMID: 17517638      PMCID: PMC1874225          DOI: 10.1073/pnas.0703509104

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  37 in total

1.  AAV vector-mediated correction of brain pathology in a mouse model of Niemann-Pick A disease.

Authors:  Marco A Passini; Shannon L Macauley; Michael R Huff; Tatyana V Taksir; Jie Bu; I-Huan Wu; Peter A Piepenhagen; James C Dodge; Lamya S Shihabuddin; Catherine R O'Riordan; Edward H Schuchman; Gregory R Stewart
Journal:  Mol Ther       Date:  2005-05       Impact factor: 11.454

2.  Gene transfer of human acid sphingomyelinase corrects neuropathology and motor deficits in a mouse model of Niemann-Pick type A disease.

Authors:  James C Dodge; Jennifer Clarke; Antonius Song; Jie Bu; Wendy Yang; Tatyana V Taksir; Denise Griffiths; Michael A Zhao; Edward H Schuchman; Seng H Cheng; Catherine R O'Riordan; Lamya S Shihabuddin; Marco A Passini; Gregory R Stewart
Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-21       Impact factor: 11.205

3.  Evasion of immune responses to introduced human acid alpha-glucosidase by liver-restricted expression in glycogen storage disease type II.

Authors:  Luis M Franco; Baodong Sun; Xiaoyi Yang; Andrew Bird; Haoyue Zhang; Ayn Schneider; Talmage Brown; Sarah P Young; Timothy M Clay; Andrea Amalfitano; Y T Chen; Dwight D Koeberl
Journal:  Mol Ther       Date:  2005-07-06       Impact factor: 11.454

4.  AAV8-mediated hepatic expression of acid sphingomyelinase corrects the metabolic defect in the visceral organs of a mouse model of Niemann-Pick disease.

Authors:  Christine M Barbon; Robin J Ziegler; Chester Li; Donna Armentano; Maribeth Cherry; Robert J Desnick; Edward H Schuchman; Seng H Cheng
Journal:  Mol Ther       Date:  2005-09       Impact factor: 11.454

5.  Effective gene therapy for an inherited CNS disease in a large animal model.

Authors:  Charles H Vite; Joseph C McGowan; Sumit N Niogi; Marco A Passini; Kenneth J Drobatz; Mark E Haskins; John H Wolfe
Journal:  Ann Neurol       Date:  2005-03       Impact factor: 10.422

6.  Intracranial delivery of CLN2 reduces brain pathology in a mouse model of classical late infantile neuronal ceroid lipofuscinosis.

Authors:  Marco A Passini; James C Dodge; Jie Bu; Wendy Yang; Qi Zhao; Dolan Sondhi; Neil R Hackett; Stephen M Kaminsky; Qinwen Mao; Lamya S Shihabuddin; Seng H Cheng; David E Sleat; Gregory R Stewart; Beverly L Davidson; Peter Lobel; Ronald G Crystal
Journal:  J Neurosci       Date:  2006-02-01       Impact factor: 6.167

7.  Efficacy of an adeno-associated virus 8-pseudotyped vector in glycogen storage disease type II.

Authors:  Baodong Sun; Haoyue Zhang; Luis M Franco; Sarah P Young; Ayn Schneider; Andrew Bird; Andrea Amalfitano; Y-T Chen; Dwight D Koeberl
Journal:  Mol Ther       Date:  2005-01       Impact factor: 11.454

8.  Improved behavior and neuropathology in the mouse model of Sanfilippo type IIIB disease after adeno-associated virus-mediated gene transfer in the striatum.

Authors:  Arnaud Cressant; Nathalie Desmaris; Lucie Verot; Thomas Bréjot; Roseline Froissart; Marie-T Vanier; Irène Maire; Jean Michel Heard
Journal:  J Neurosci       Date:  2004-11-10       Impact factor: 6.167

9.  Functional correction of CNS phenotypes in a lysosomal storage disease model using adeno-associated virus type 4 vectors.

Authors:  Gumei Liu; Inês Martins; John A Wemmie; John A Chiorini; Beverly L Davidson
Journal:  J Neurosci       Date:  2005-10-12       Impact factor: 6.167

10.  Genetically corrected autologous stem cells engraft, but host immune responses limit their utility in canine alpha-L-iduronidase deficiency.

Authors:  C Lutzko; S Kruth; A C Abrams-Ogg; K Lau; L Li; B R Clark; C Ruedy; S Nanji; R Foster; D Kohn; R Shull; I D Dubé
Journal:  Blood       Date:  1999-03-15       Impact factor: 22.113

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  42 in total

Review 1.  Fabry disease, enzyme replacement therapy and the significance of antibody responses.

Authors:  Patrick B Deegan
Journal:  J Inherit Metab Dis       Date:  2011-10-25       Impact factor: 4.982

Review 2.  Gene therapy for the neurological manifestations in lysosomal storage disorders.

Authors:  Seng H Cheng
Journal:  J Lipid Res       Date:  2014-03-29       Impact factor: 5.922

3.  Improved induction of immune tolerance to factor IX by hepatic AAV-8 gene transfer.

Authors:  Mario Cooper; Sushrusha Nayak; Brad E Hoffman; Cox Terhorst; Ou Cao; Roland W Herzog
Journal:  Hum Gene Ther       Date:  2009-07       Impact factor: 5.695

Review 4.  Genetic therapy for the nervous system.

Authors:  William J Bowers; Xandra O Breakefield; Miguel Sena-Esteves
Journal:  Hum Mol Genet       Date:  2011-03-23       Impact factor: 6.150

5.  Therapeutic approaches for lysosomal storage diseases.

Authors:  Gregory M Pastores
Journal:  Ther Adv Endocrinol Metab       Date:  2010-08       Impact factor: 3.565

Review 6.  The liver works as a school to educate regulatory immune cells.

Authors:  Fenglei Li; Zhigang Tian
Journal:  Cell Mol Immunol       Date:  2013-04-22       Impact factor: 11.530

Review 7.  Progress and prospects: immune responses to viral vectors.

Authors:  S Nayak; R W Herzog
Journal:  Gene Ther       Date:  2009-11-12       Impact factor: 5.250

Review 8.  Gene Therapy for the Treatment of Neurological Disorders: Metabolic Disorders.

Authors:  Dominic J Gessler; Guangping Gao
Journal:  Methods Mol Biol       Date:  2016

9.  AAV-mediated gene delivery in adult GM1-gangliosidosis mice corrects lysosomal storage in CNS and improves survival.

Authors:  Rena C Baek; Marike L D Broekman; Stanley G Leroy; Laryssa A Tierney; Michael A Sandberg; Alessandra d'Azzo; Thomas N Seyfried; Miguel Sena-Esteves
Journal:  PLoS One       Date:  2010-10-18       Impact factor: 3.240

10.  Tolerance induction to cytoplasmic beta-galactosidase by hepatic AAV gene transfer: implications for antigen presentation and immunotoxicity.

Authors:  Ashley T Martino; Sushrusha Nayak; Brad E Hoffman; Mario Cooper; Gongxian Liao; David M Markusic; Barry J Byrne; Cox Terhorst; Roland W Herzog
Journal:  PLoS One       Date:  2009-08-04       Impact factor: 3.240

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