Effective repeat administration with adenovirus vectors to the muscle
- 1 April 2000
- journal article
- research article
- Published by Springer Nature in Gene Therapy
- Vol. 7 (7) , 587-595
- https://doi.org/10.1038/sj.gt.3301137
Abstract
Effective repeat administration of adenovirus vectors following intranasal or intravenous delivery is hindered by a strong neutralizing antibody response to the vector. Intramuscular administration of adenovirus vectors elicited a neutralizing antibody response that peaked between 14 and 21 days after infection. However, effective repeat intramuscular administration of adenovirus vectors was not hindered by the presence of neutralizing antibodies in the serum. Surprisingly, β-galactosidase expression in the skeletal muscle of immunized mice was equivalent to that observed in control mice. As expected, these serum neutralizing antibodies effectively blocked repeat administration of adenovirus vectors when delivered via the intravenous route. These results were observed in both C57BL/6 and Balb/c mice and thus do not appear to be strain specific. Successful repeat administration of adenovirus vectors to skeletal muscle has significant implications for the use of adenovirus vectors clinically and for increasing the safety and efficacy of adenovirus vector gene delivery.Keywords
This publication has 54 references indexed in Scilit:
- Characterization of the Immune Response After Local Delivery of Recombinant Adenovirus in Murine Pancreas and Successful Strategies for ReadministrationHuman Gene Therapy, 1997
- Adenovirus-mediated gene transfer: influence of transgene, mouse strain and type of immune response on persistence of transgene expressionGene Therapy, 1997
- Nondepleting Anti-CD4 Antibody Treatment Prolongs Lung-Directed E1-Deleted Adenovirus-Mediated Gene Expression in RatsHuman Gene Therapy, 1996
- Adenovirus targeted to heparan-containing receptors increases its gene delivery efficiency to multiple cell typesNature Biotechnology, 1996
- Immune responses to transgene–encoded proteins limit the stability of gene expression after injection of replication–defective adenovirus vectorsNature Medicine, 1996
- Use of Transient CD4 Lymphocyte Depletion to Prolong Transgene Expression of E1-Deleted Adenoviral VectorsHuman Gene Therapy, 1996
- “Sero-Switch” Adenovirus-MediatedIn VivoGene Transfer: Circumvention of Anti-Adenovirus Humoral Immune Defenses Against Repeat Adenovirus Vector Administration by Changing the Adenovirus SerotypeHuman Gene Therapy, 1996
- Long–term hepatic adenovirus–mediated gene expression in mice following CTLA4Ig administrationNature Genetics, 1995
- Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy.Proceedings of the National Academy of Sciences, 1994
- Role of Adenovirus Antigens in the Induction of Virus Neutralizing AntibodyJournal of General Virology, 1968