| Literature DB >> 15963932 |
John R Greenland1, Huining Liu, David Berry, Daniel G Anderson, Woong-Ki Kim, Darrell J Irvine, Robert Langer, Norman L Letvin.
Abstract
Increased in vivo expression of intramuscularly delivered plasmid DNA will be essential for clinical success in gene therapy and plasmid DNA vaccination. We screened polymers from a library of beta-amino esters for their ability to augment transgene expression as measured by beta-galactosidase activity and cellular immune responses. Among the candidates identified in this screen, poly[(1,6-di(acryloxyethoxy)hexane)-co-(4-aminobutanol)] enhanced plasmid DNA transgene expression by sevenfold (P=0.0001) and its immunogenicity by 70% (P=0.03). We found that polymers with moderately hydrophobic backbones and terminal alcohol groups facilitated transfection most effectively in vivo. We also observed a log-linear correlation (R2=0.93) between peak cellular immune responses and transgene activity in all evaluated polymer-plasmid DNA formulations, clarifying the relationship between immunogenicity and the quantity of expressed antigen.Entities:
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Year: 2005 PMID: 15963932 DOI: 10.1016/j.ymthe.2005.01.021
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454