Adenoviral vectors: development and application
- 1 October 1997
- journal article
- Published by Taylor & Francis in Expert Opinion on Investigational Drugs
- Vol. 6 (10) , 1419-1457
- https://doi.org/10.1517/13543784.6.10.1419
Abstract
One of the prerequisites for the successful application of gene vaccination and therapy is the development of efficient gene delivery vectors. The rate-limiting nature of vectors was clearly manifested during the first wave of gene therapy testing, resulting in the demand for more effective and suitable vector systems. Adenoviral (Ad) vectors have recently played a central role in the development of gene-vector technology due to their practical advantages and potential applications. A large number of preclinical and clinical studies both have generated an overwhelming amount of data and literature on this vector system. It is the intention of this article to provide a systematic and broad spectrum review of this system, outlining the principle, potential, and limitations, and evaluating the rational development of this delivery approach. Recombinant adenoviruses (Ad), helper cell lines, and related technologies have been developed and applied to many indications owing to progress in virological research, ...Keywords
This publication has 168 references indexed in Scilit:
- Immunosuppression by FK506 Markedly Prolongs Expression of Adenovirus-Delivered Transgene in Skeletal Muscles of Adult Dystrophic [mdx] MiceBiochemical and Biophysical Research Communications, 1995
- Antigenic homogeneity among the adenovirus hexon types of subgenus CArchiv für die gesamte Virusforschung, 1995
- Prolonged Transgene Expression in Cotton Rat Lung with Recombinant Adenoviruses Defective in E2aHuman Gene Therapy, 1994
- Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosisNature Genetics, 1994
- Evaluation of the Efficacy and Safety ofIn Vitro, Adenovirus-Mediated Transfer of the Human Cystic Fibrosis Transmembrane Conductance Regulator cDNAHuman Gene Therapy, 1994
- Gene Therapy for Cystic Fibrosis Using E1-Deleted Adenovirus: A Phase I Trial in the Nasal Cavity. University of North Carolina at Chapel Hill, Chapel Hill, North CarolinaHuman Gene Therapy, 1994
- Adenovirus-mediated correction of the genetic defect in hepatocytes from patients with familial hypercholesterolemiaSomatic Cell and Molecular Genetics, 1993
- Retroviral‐mediated transfer of a dystrophin minigene into mdx mouse myoblasts in vitroFEBS Letters, 1992
- Nuclear factor III, a novel sequence-specific DNA-binding protein from HeLa cells stimulating adenovirus DNA replicationNature, 1986
- Bacteriophage P1 site-specific recombinationJournal of Molecular Biology, 1981