Literature DB >> 16409124

Efficient AAV1-AAV2 hybrid vector for gene therapy of hemophilia.

Bernd Hauck1, Ray Ruian Xu, Jing Xie, Wenman Wu, Qiulan Ding, Matthew Sipler, Hongli Wang, Ling Chen, J Fraser Wright, Weidong Xiao.   

Abstract

Adeno-associated virus (AAV) serotype 1 (AAV1) has been shown to be more effective than the well-studied AAV serotype 2 (AAV2) in muscle gene transfer. Replacement of amino acids 350 to 430 of AAV2 VP1 with the corresponding amino acids from VP1 of AAV1 resulted in a hybrid vector, termed AAV-221-IV, which behaved similarly to AAV1 in vitro and in vivo in muscle. Intramuscular injection of 1x10(11) vector particles per mouse of hybrid vector carrying a human FIX transgene in CD4 knockout mice resulted in an average level of human FIX in the plasma of 450 ng/ml, 4- to 10-fold higher than in mice injected with an AAV2 vector carrying the same transgene, and 80% of the transgene levels in animals treated with the same dose of AAV1. DNA analysis of injected muscle showed a 10-fold higher copy number after gene delivery by the hybrid vector compared with AAV2. A comparison of total DNA versus DNA from intact virus particles suggests a higher stability of hybrid virus particles. These results suggest that changes in the AAV capsid have an effect on virus-cell receptor interaction, and also influence trafficking and processing of the virus particle in the cell. This "hybrid vector" retains the heparin-binding sites of AAV2 and, therefore, can be purified by passage through a heparin-Sepharose column with the same efficiency as AAV2. When tested in vivo, either in CD4 knockout mice or in a hemophilic mouse model, the heparin-purified hybrid vector showed >10-fold higher activity than similarly purified AAV2. This demonstrates the utility of this hybrid vector in the performance of large-scale heparin column purification to generate a vector with a high expression profile for muscle-directed gene delivery. Initiation of clinical studies with this hybrid vector may be facilitated because it differs from AAV2 by only nine amino acids.

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Year:  2006        PMID: 16409124      PMCID: PMC2628442          DOI: 10.1089/hum.2006.17.46

Source DB:  PubMed          Journal:  Hum Gene Ther        ISSN: 1043-0342            Impact factor:   5.695


  44 in total

Review 1.  Gene therapy for the hemophilias.

Authors:  M A Kay; K High
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-31       Impact factor: 11.205

2.  Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield.

Authors:  S Zolotukhin; B J Byrne; E Mason; I Zolotukhin; M Potter; K Chesnut; C Summerford; R J Samulski; N Muzyczka
Journal:  Gene Ther       Date:  1999-06       Impact factor: 5.250

3.  Novel tools for production and purification of recombinant adenoassociated virus vectors.

Authors:  D Grimm; A Kern; K Rittner; J A Kleinschmidt
Journal:  Hum Gene Ther       Date:  1998-12-10       Impact factor: 5.695

4.  Gene therapy vectors based on adeno-associated virus type 1.

Authors:  W Xiao; N Chirmule; S C Berta; B McCullough; G Gao; J M Wilson
Journal:  J Virol       Date:  1999-05       Impact factor: 5.103

5.  Persistent expression of canine factor IX in hemophilia B canines.

Authors:  H Chao; R Samulski; D Bellinger; P Monahan; T Nichols; C Walsh
Journal:  Gene Ther       Date:  1999-10       Impact factor: 5.250

Review 6.  Recent developments in adeno-associated virus vector technology.

Authors:  Hildegard Büning; Luca Perabo; Oliver Coutelle; Sibille Quadt-Humme; Michael Hallek
Journal:  J Gene Med       Date:  2008-07       Impact factor: 4.565

7.  Human fibroblast growth factor receptor 1 is a co-receptor for infection by adeno-associated virus 2.

Authors:  K Qing; C Mah; J Hansen; S Zhou; V Dwarki; A Srivastava
Journal:  Nat Med       Date:  1999-01       Impact factor: 53.440

8.  AlphaVbeta5 integrin: a co-receptor for adeno-associated virus type 2 infection.

Authors:  C Summerford; J S Bartlett; R J Samulski
Journal:  Nat Med       Date:  1999-01       Impact factor: 53.440

9.  Cloning and characterization of adeno-associated virus type 5.

Authors:  J A Chiorini; F Kim; L Yang; R M Kotin
Journal:  J Virol       Date:  1999-02       Impact factor: 5.103

10.  Syngeneic transplantation of hematopoietic stem cells that are genetically modified to express factor VIII in platelets restores hemostasis to hemophilia A mice with preexisting FVIII immunity.

Authors:  Qizhen Shi; Scot A Fahs; David A Wilcox; Erin L Kuether; Patricia A Morateck; Nicole Mareno; Hartmut Weiler; Robert R Montgomery
Journal:  Blood       Date:  2008-05-21       Impact factor: 22.113

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  11 in total

Review 1.  E Pluribus Unum: 50 Years of Research, Millions of Viruses, and One Goal--Tailored Acceleration of AAV Evolution.

Authors:  Dirk Grimm; Sergei Zolotukhin
Journal:  Mol Ther       Date:  2015-09-21       Impact factor: 11.454

2.  Phase 1 gene therapy for Duchenne muscular dystrophy using a translational optimized AAV vector.

Authors:  Dawn E Bowles; Scott W J McPhee; Chengwen Li; Steven J Gray; Jade J Samulski; Angelique S Camp; Juan Li; Bing Wang; Paul E Monahan; Joseph E Rabinowitz; Joshua C Grieger; Lakshmanan Govindasamy; Mavis Agbandje-McKenna; Xiao Xiao; R Jude Samulski
Journal:  Mol Ther       Date:  2011-11-08       Impact factor: 11.454

3.  Existence of transient functional double-stranded DNA intermediates during recombinant AAV transduction.

Authors:  Jinhui Wang; Jing Xie; Hui Lu; Lingxia Chen; Bernd Hauck; Richard Jude Samulski; Weidong Xiao
Journal:  Proc Natl Acad Sci U S A       Date:  2007-07-30       Impact factor: 11.205

4.  An adeno-associated virus vector efficiently and specifically transduces mouse skeletal muscle.

Authors:  Isao Murakami; Takamasa Takeuchi; Mayuyo Mori-Uchino; Seiichiro Mori; Takuma Fujii; Daisuke Aoki; Keiichi Nakagawa; Tadahito Kanda
Journal:  Mol Biotechnol       Date:  2011-09       Impact factor: 2.695

Review 5.  Adeno-associated virus as a gene therapy vector: strategies to neutralize the neutralizing antibodies.

Authors:  Majid Lotfinia; Meghdad Abdollahpour-Alitappeh; Behzad Hatami; Mohammad Reza Zali; Morteza Karimipoor
Journal:  Clin Exp Med       Date:  2019-05-03       Impact factor: 3.984

6.  In vivo enrichment of genetically manipulated platelets corrects the murine hemophilic phenotype and induces immune tolerance even using a low multiplicity of infection.

Authors:  J A Schroeder; Y Chen; J Fang; D A Wilcox; Q Shi
Journal:  J Thromb Haemost       Date:  2014-07-17       Impact factor: 5.824

7.  Development of Patient-specific AAV Vectors After Neutralizing Antibody Selection for Enhanced Muscle Gene Transfer.

Authors:  Chengwen Li; Shuqing Wu; Blake Albright; Matthew Hirsch; Wuping Li; Yu-Shan Tseng; Mavis Agbandje-McKenna; Scott McPhee; Aravind Asokan; R Jude Samulski
Journal:  Mol Ther       Date:  2015-07-29       Impact factor: 11.454

8.  Syngeneic transplantation of hematopoietic stem cells that are genetically modified to express factor VIII in platelets restores hemostasis to hemophilia A mice with preexisting FVIII immunity.

Authors:  Qizhen Shi; Scot A Fahs; David A Wilcox; Erin L Kuether; Patricia A Morateck; Nicole Mareno; Hartmut Weiler; Robert R Montgomery
Journal:  Blood       Date:  2008-05-21       Impact factor: 22.113

9.  Enhanced factor VIII heavy chain for gene therapy of hemophilia A.

Authors:  Lingxia Chen; Hui Lu; Jinhui Wang; Rita Sarkar; Xiao Yang; Hongli Wang; Katherine A High; Weidong Xiao
Journal:  Mol Ther       Date:  2009-01-06       Impact factor: 11.454

10.  Single amino acid insertion allows functional transduction of murine hepatocytes with human liver tropic AAV capsids.

Authors:  Marti Cabanes-Creus; Renina Gale Navarro; Sophia H Y Liao; Grober Baltazar; Matthieu Drouyer; Erhua Zhu; Suzanne Scott; Clement Luong; Laurence O W Wilson; Ian E Alexander; Leszek Lisowski
Journal:  Mol Ther Methods Clin Dev       Date:  2021-04-24       Impact factor: 6.698

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