Catheter-based adenovirus-mediated local intravascular gene delivery of a soluble TGF-beta type II receptor using an Infiltrator in porcine coronary arteries: efficacy and complications.
- Author:
Ick Mo CHUNG
1
;
Hikaru UENO
;
Young Mi KIM PAK
;
Joon Woo KIM
;
Dong Hoon CHOI
;
Gil Ja SHIN
;
Woo Ick YANG
;
Yang Soo JANG
Author Information
1. Division of Cardiology, Ewha Womans University School of Medicine, 70 Jongro-Gu, Jongro-6 Ga, Seoul, Korea. ickmo@mm.ewha.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
gene therapy;
local delivery;
transforming growth factor b receptors;
extracellular matrix;
coronary restenosis;
catheterization
- MeSH:
Adenoviridae/*genetics;
Animals;
*Catheters, Indwelling;
Coronary Vessels/*metabolism/pathology;
Female;
Gene Expression;
Gene Therapy/*adverse effects/*methods/mortality;
*Gene Transfer Techniques;
Genetic Vectors/*administration & dosage;
Inflammation/etiology;
Receptors, Transforming Growth Factor beta/analysis/*metabolism;
Swine;
Transgenes;
beta-Galactosidase/genetics/metabolism
- From:Experimental & Molecular Medicine
2002;34(4):299-307
- CountryRepublic of Korea
- Language:English
-
Abstract:
Enhanced extracellular matrix (ECM) accumulation is an important finding in human restenotic arterial neointima after angioplasty. Transforming growth factor b1(TGF-beta1) is known to regulate the synthesis and turnover of a variety of ECM components, and may play an important role in restenosis. Recombinant adenoviral vector expressing an ectodomain of the TGF-beta type II receptor fused to the human immunoglobulin Fc portion (AdT beta-ExR) inhibits the action of TGF-beta probably either by adsorbing TGF-beta or by acting as a dominant negative receptor. We carried out a catheter-based local adenovirus mediated gene delivery using an Infiltrator in porcine coronary arteries to know the pattern of gene expression, efficacy and procedural complications. Twenty four coronary arteries in 13 pigs were used for intravascular gene delivery by intramural injection with either AdT beta-ExR or adenovirus expressing b-galactosidase (AdCALacZ). Direct immunofluorescent staining and reverse transcription polymerase chain reaction (RTPCR) were used for detection of type II TGF-beta receptor and its mRNA respectively. X-Gal histochemistry was performed to identify b-galactosidase. Both soluble TGF-beta receptor and b-galactosidase were expressed locally in the media and adventita at injected arterial segments without any significant dissemination to remote area. Intravascular gene transfection performed with various titer of each adenoviral vector showed that AdT beta-ExR of 5x10(8) pfu and AdCALacZ of 2.5 x 10(8) pfu were the minimum titer for the expression of each transgene. Infiltration of CD3 positive T cells was detected by immunohistochemical staining in the area of each transgene expression, and tends to decrease over time after gene delivery. Pathological study of 24 treated arteries showed complications such as disruption of external elastic lamina with hemorrhage (n = 4), minimal disruption of internal elastic lamina and endothelial layer, and medial thickening. In conclusion, catheter-based local intravascular gene delivery of adenoviral vector is feasible and effective in a selected artery, but must be undertaken with caution due to possible lethal complications. Local delivery of soluble TGF-beta type II receptor in this way may provide an effective intravascular gene therapy to inhibit TGF-beta signal pathway without any significant systemic side effect.
