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CpG-free plasmids confer reduced inflammation and sustained pulmonary gene expression.

Authors :
Hyde, Stephen C.
Pringle, Ian A.
Abdullah, Syahril
Lawton, Anna E.
Davies, Lee A.
Varathalingam, Anusha
Nunez-Alonso, Graciela A.
Green, Anne Marie
Bazzani, Reto P.
Sumner-Jones, Stephanie G.
Chan, Mario
Hong, Yu Li
Yew, Nelson S.
Cheng, Seng H.
Boyd, Christopher A.
Davies, Jane C.
Griesenbach, Uta
Porteous, David John
Sheppard, David N.
Munkonge, Felix M.
Alton, Eric W. F. W.
Gill, Deborah R.
Hyde, Stephen C.
Pringle, Ian A.
Abdullah, Syahril
Lawton, Anna E.
Davies, Lee A.
Varathalingam, Anusha
Nunez-Alonso, Graciela A.
Green, Anne Marie
Bazzani, Reto P.
Sumner-Jones, Stephanie G.
Chan, Mario
Hong, Yu Li
Yew, Nelson S.
Cheng, Seng H.
Boyd, Christopher A.
Davies, Jane C.
Griesenbach, Uta
Porteous, David John
Sheppard, David N.
Munkonge, Felix M.
Alton, Eric W. F. W.
Gill, Deborah R.
Publication Year :
2008

Abstract

Pulmonary delivery of plasmid DNA (pDNA)/cationic liposome complexes is associated with an acute unmethylated CG dinucleotide (CpG)-mediated inflammatory response and brief duration of transgene expression. We demonstrate that retention of even a single CpG in pDNA is sufficient to elicit an inflammatory response, whereas CpG-free pDNA vectors do not. Using a CpG-free pDNA expression vector, we achieved sustained (≥56 d) in vivo transgene expression in the absence of lung inflammation.

Details

Database :
OAIster
Notes :
application/pdf, English, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1050090343
Document Type :
Electronic Resource