Literature DB >> 23902403

Transgene expression up to 7 years in nonhuman primates following hepatic transduction with helper-dependent adenoviral vectors.

Nicola Brunetti-Pierri1, Thomas Ng, David Iannitti, William Cioffi, Gary Stapleton, Mark Law, John Breinholt, Donna Palmer, Nathan Grove, Karen Rice, Cassondra Bauer, Milton Finegold, Arthur Beaudet, Charles Mullins, Philip Ng.   

Abstract

Helper-dependent adenoviral vectors (HDAd) have been shown to mediate a considerably longer duration of transgene expression than first-generation adenoviral vectors. We have previously shown that transgene expression from HDAd-transduced hepatocytes can persist at high levels for up to 2.6 years in nonhuman primates following a single-vector administration. Because duration of transgene expression and long-term toxicity are critical for risk:benefit assessment, we have continued to monitor these animals. We report here that transgene expression has persisted for the entire observation period of up to 7 years for all animals without long-term adverse effects. However, in all cases, transgene expression level slowly declined over time to less than 10% of peak values by the end of the observation period but remained 2.3-111-fold above baseline values. These results will provide important information for a more informed risk:benefit assessment before clinical application of HDAd.

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Year:  2013        PMID: 23902403      PMCID: PMC3746245          DOI: 10.1089/hum.2013.071

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


  14 in total

1.  Improved system for helper-dependent adenoviral vector production.

Authors:  Donna Palmer; Philip Ng
Journal:  Mol Ther       Date:  2003-11       Impact factor: 11.454

2.  Physical and infectious titers of helper-dependent adenoviral vectors: a method of direct comparison to the adenovirus reference material.

Authors:  Donna J Palmer; Philip Ng
Journal:  Mol Ther       Date:  2004-10       Impact factor: 11.454

3.  Sustained phenotypic correction of canine hemophilia B after systemic administration of helper-dependent adenoviral vector.

Authors:  Nicola Brunetti-Pierri; Timothy C Nichols; Stephanie McCorquodale; Elizabeth Merricks; Donna J Palmer; Arthur L Beaudet; Philip Ng
Journal:  Hum Gene Ther       Date:  2005-07       Impact factor: 5.695

4.  Lifetime correction of genetic deficiency in mice with a single injection of helper-dependent adenoviral vector.

Authors:  I H Kim; A Józkowicz; P A Piedra; K Oka; L Chan
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-30       Impact factor: 11.205

5.  Local delivery of a viral vector mitigates neutralization by antiviral antibodies and results in efficient transduction of rabbit liver.

Authors:  Bradley L Hodges; Kristin M Taylor; Qiuming Chu; Samantha E Scull; Rebecca G Serriello; Scott C Anderson; Fei Wang; Ronald K Scheule
Journal:  Mol Ther       Date:  2005-08-31       Impact factor: 11.454

6.  "Stealth" adenoviruses blunt cell-mediated and humoral immune responses against the virus and allow for significant gene expression upon readministration in the lung.

Authors:  M A Croyle; N Chirmule; Y Zhang; J M Wilson
Journal:  J Virol       Date:  2001-05       Impact factor: 5.103

7.  Balloon catheter delivery of helper-dependent adenoviral vector results in sustained, therapeutic hFIX expression in rhesus macaques.

Authors:  Nicola Brunetti-Pierri; Aimee Liou; Priti Patel; Donna Palmer; Nathan Grove; Milton Finegold; Pasquale Piccolo; Elizabeth Donnachie; Karen Rice; Arthur Beaudet; Charles Mullins; Philip Ng
Journal:  Mol Ther       Date:  2012-07-24       Impact factor: 11.454

8.  Lifespan in captive baboons is heritable.

Authors:  Lisa J Martin; Michael C Mahaney; Anne M Bronikowski; K Dee Carey; Bennett Dyke; Anthony G Comuzzie
Journal:  Mech Ageing Dev       Date:  2002-09       Impact factor: 5.432

9.  Improved hepatic transduction, reduced systemic vector dissemination, and long-term transgene expression by delivering helper-dependent adenoviral vectors into the surgically isolated liver of nonhuman primates.

Authors:  Nicola Brunetti-Pierri; Thomas Ng; David A Iannitti; Donna J Palmer; Arthur L Beaudet; Milton J Finegold; K Dee Carey; William G Cioffi; Philip Ng
Journal:  Hum Gene Ther       Date:  2006-04       Impact factor: 5.695

10.  Lifelong elimination of hyperbilirubinemia in the Gunn rat with a single injection of helper-dependent adenoviral vector.

Authors:  Gabriele Toietta; Viraj P Mane; Wilma S Norona; Milton J Finegold; Philip Ng; Antony F McDonagh; Arthur L Beaudet; Brendan Lee
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-07       Impact factor: 11.205

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  33 in total

Review 1.  Innate immunity to adenovirus: lessons from mice.

Authors:  Svetlana Atasheva; Jia Yao; Dmitry M Shayakhmetov
Journal:  FEBS Lett       Date:  2019-12-08       Impact factor: 4.124

Review 2.  Gene therapy with helper-dependent adenoviral vectors: lessons from studies in large animal models.

Authors:  Nicola Brunetti-Pierri; Philip Ng
Journal:  Virus Genes       Date:  2017-06-07       Impact factor: 2.332

3.  Apo A-I (Apolipoprotein A-I) Vascular Gene Therapy Provides Durable Protection Against Atherosclerosis in Hyperlipidemic Rabbits.

Authors:  Bradley K Wacker; Nagadhara Dronadula; Lianxiang Bi; Alexis Stamatikos; David A Dichek
Journal:  Arterioscler Thromb Vasc Biol       Date:  2017-11-09       Impact factor: 8.311

4.  Restoration of the serum level of SERPINF1 does not correct the bone phenotype in Serpinf1 null mice.

Authors:  Abbhirami Rajagopal; Erica P Homan; Kyu Sang Joeng; Masataka Suzuki; Terry Bertin; Racel Cela; Elda Munivez; Brian Dawson; Ming-Ming Jiang; Frank Gannon; Susan Crawford; Brendan H Lee
Journal:  Mol Genet Metab       Date:  2015-12-02       Impact factor: 4.797

5.  Helper-dependent adenovirus achieve more efficient and persistent liver transgene expression in non-human primates under immunosuppression.

Authors:  C Unzu; I Melero; S Hervás-Stubbs; A Sampedro; U Mancheño; A Morales-Kastresana; I Serrano-Mendioroz; R E de Salamanca; A Benito; A Fontanellas
Journal:  Gene Ther       Date:  2015-07-23       Impact factor: 5.250

6.  In Vivo Gene Transfer to the Rabbit Common Carotid Artery Endothelium.

Authors:  Bradley K Wacker; Lianxiang Bi; David A Dichek
Journal:  J Vis Exp       Date:  2018-05-06       Impact factor: 1.355

7.  Adenovirus-Vectored Broadly Neutralizing Antibodies Directed Against gp120 Prevent Human Immunodeficiency Virus Type 1 Acquisition in Humanized Mice.

Authors:  Shan Liu; Andrew Jackson; Jagadish Beloor; Priti Kumar; Richard E Sutton
Journal:  Hum Gene Ther       Date:  2015-08-11       Impact factor: 5.695

8.  Long-term, high-level hepatic secretion of acid α-glucosidase for Pompe disease achieved in non-human primates using helper-dependent adenovirus.

Authors:  D P W Rastall; S S Seregin; Y A Aldhamen; L M Kaiser; C Mullins; A Liou; F Ing; C Pereria-Hicks; S Godbehere-Roosa; D Palmer; P Ng; A Amalfitano
Journal:  Gene Ther       Date:  2016-07-01       Impact factor: 5.250

Review 9.  Current and Future Treatments for Lysosomal Storage Disorders.

Authors:  David P W Rastall; Andrea Amalfitano
Journal:  Curr Treat Options Neurol       Date:  2017-11-04       Impact factor: 3.598

Review 10.  Retargeting adenoviruses for therapeutic applications and vaccines.

Authors:  Michael A Barry; Jeffrey D Rubin; Shao-Chia Lu
Journal:  FEBS Lett       Date:  2020-02-03       Impact factor: 4.124

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