For COVID-19 vaccine updates, please review our information guide. For patient eligibility and scheduling availability, please visit VaccineTogetherNY.org.

The impact of developmental stage, route of administration and the immune system on adenovirus-mediated gene transfer.

TitleThe impact of developmental stage, route of administration and the immune system on adenovirus-mediated gene transfer.
Publication TypeJournal Article
Year of Publication1994
AuthorsKass-Eisler A, Falck-Pedersen E, Elfenbein DH, Alvira M, Buttrick PM, Leinwand LA
JournalGene Ther
Volume1
Issue6
Pagination395-402
Date Published1994 Nov
ISSN0969-7128
KeywordsAdenoviridae, Animals, Chloramphenicol O-Acetyltransferase, Gene Expression, Gene Transfer Techniques, Genes, Reporter, Genetic Therapy, Immune System, Rats, Rats, Sprague-Dawley, Recombination, Genetic, T-Lymphocytes, Time Factors, Tissue Distribution
Abstract

Important aspects of successful adenovirus gene transfer include the amount and persistence of gene expression, the ability to readminister virus and the localization of virus-directed gene expression to target organs. Our objective in this study was to use a single recombinant adenovirus bearing a quantifiable reporter gene [chloramphenicol acetyltransferase (CAT)] to establish the parameters which define the limits of adenovirus gene expression in a rat model. First, we determined how the route of virus administration affected the amount, duration and distribution of expression in different tissues and in rats of different developmental stages. All routes resulted in infection of all tissues tested. Surprisingly, the most efficient and widespread gene transfer was achieved by intracardiac muscle injection. The high levels of CAT protein that can be produced in a liver (< or = 1.7 mg) or a heart (< or = 196 micrograms) 5 days after infection suggest that the amount of gene product will not be a limitation in the use of adenovirus. Following peak activity at 5 days after infection, a gradual decline of CAT expression was observed in all tissues assayed; by 80 days neither CAT activity nor adenovirus DNA were detectable. In addition, adults could not be boosted by a second administration of virus, presumably due to the presence of high levels of neutralizing antibodies. The limited persistence of gene expression could be circumvented when virus was injected into neonates. Blocking T lymphocyte expansion by cyclosporine enhanced the persistence of CAT gene product over a 25-day period in heart and lung but not in liver compared with control animals.(ABSTRACT TRUNCATED AT 250 WORDS)

Alternate JournalGene Ther
PubMed ID7584105
Grant ListGM29090 / GM / NIGMS NIH HHS / United States
GM41967 / GM / NIGMS NIH HHS / United States
T32AG0092-05 / AG / NIA NIH HHS / United States

Weill Cornell Medicine Microbiology and Immunology 1300 York Avenue, Box 62 New York, NY 10065 Phone: (212) 746-6505 Fax: (212) 746-8587