Image-guided, Lobe-specific Hydrodynamic Gene Delivery to Swine Liver

被引:71
作者
Kamimura, Kenya [1 ]
Suda, Takeshi [1 ]
Xu, Wei [1 ]
Zhang, Guisheng [1 ]
Liu, Dexi [1 ]
机构
[1] Univ Pittsburgh, Dept Pharmaceut Sci, Sch Pharm, Pittsburgh, PA 15261 USA
关键词
DEPENDENT ADENOVIRAL VECTORS; NAKED PLASMID DNA; PIG-LIVER; THERAPY; EXPRESSION; INJECTION;
D O I
10.1038/mt.2008.294
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Image-guided, lobe-specific hydrodynamic gene delivery to liver was assessed in pigs. The procedure involved image-guided insertion of a balloon catheter to the hepatic vein of the selected lobe from the jugular vein and hydrodynamic injection of plasmid DNA using a newly developed computer-controlled injection device. We demonstrated that the impact of the procedure was regional with minimal effects on neighboring lobes. Level of gene expression resulted from the procedure was 10(7) relative light units (RLU)/mg in the targeted lobes and 10(2)-10(5) RLU/mg in the nontargeted lobes 4 hours after hydrodynamic injection of pCMV-Luc plasmids. Occlusion of blood flow in the inferior vena cava (IVC) or IVC plus portal vein (PV) was effective in elevating hydrodynamic pressure in the targeted vasculature but did not enhance gene delivery efficiency. Physiological examination on pigs with IVC occlusion revealed transient decreases of blood pressure and respiration rate. Removal of occlusion from IVC resulted in a rapid and transient increase in heart rate. Occlusion of the PV and hepatic vein showed no effect on physiological and cardiac activities. No major changes in serum composition were observed. These results suggest that (i) image-guided, lobe-specific hydrodynamic procedure is effective for regional gene delivery to liver, (ii) blockade in IVC should be avoided for hydrodynamic gene delivery to the liver, and (iii) clinical application of hydrodynamic gene delivery to liver is feasible.
引用
收藏
页码:491 / 499
页数:9
相关论文
共 18 条
[1]  
ABDELAZIZ YI, 1972, P ASE UI S CLOS RANG, P1
[2]   Pig liver gene therapy by noninvasive interventionist catheterism [J].
Alino, S. F. ;
Herrero, M. J. ;
Noguera, I. ;
Dasi, F. ;
Sanchez, M. .
GENE THERAPY, 2007, 14 (04) :334-343
[3]   Increased hepatic transduction with reduced systemic dissemination and proinflammatory cytokines following hydrodynamic injection of helper-dependent adenoviral vectors [J].
Brunetti-Pierri, N ;
Palmer, DJ ;
Mane, V ;
Finegold, M ;
Beaudet, AL ;
Ng, P .
MOLECULAR THERAPY, 2005, 12 (01) :99-106
[4]   Pseudo-hydrodynamic delivery of helper-dependent adenoviral vectors into non-human primates for liver-directed gene therapy [J].
Brunetti-Pierri, Nicola ;
Stapleton, Gary E. ;
Palmer, Donna J. ;
Zuo, Yu ;
Mane, Viraj P. ;
Finegold, Milton J. ;
Beaudet, Arthur L. ;
Leland, Michelle M. ;
Mullins, Charles E. ;
Ng, Philip .
MOLECULAR THERAPY, 2007, 15 (04) :732-740
[5]   Prolonged liver-specific transgene expression by a non-primate lentiviral vector [J].
Condiotti, R ;
Curran, MA ;
Nolan, GP ;
Giladi, H ;
Ketzinel-Gilad, M ;
Gross, E ;
Galun, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 320 (03) :998-1006
[6]   Development of catheter-based procedures for transducing the isolated rabbit liver with plasmid DNA [J].
Eastman, SJ ;
Baskin, KM ;
Hodges, BL ;
Chu, QM ;
Gates, A ;
Dreusicke, R ;
Anderson, S ;
Scheule, RK .
HUMAN GENE THERAPY, 2002, 13 (17) :2065-2077
[7]   Hydrodynamic gene delivery to the pig liver via an isolated segment of the inferior vena cava [J].
Fabre, J. W. ;
Grehan, A. ;
Whitehorne, M. ;
Sawyer, G. J. ;
Dong, X. ;
Salehi, S. ;
Eckley, L. ;
Zhang, X. ;
Seddon, M. ;
Shah, A. M. ;
Davenport, M. ;
Rela, M. .
GENE THERAPY, 2008, 15 (06) :452-462
[8]   Gene therapy progress and prospects: Hydrodynamic gene delivery [J].
Herweijer, H. ;
Wolff, J. A. .
GENE THERAPY, 2007, 14 (02) :99-107
[9]   Crossing the bridge: large animal models in translational transplantation research [J].
Kirk, AD .
IMMUNOLOGICAL REVIEWS, 2003, 196 (01) :176-196
[10]   Special stains in diagnostic liver pathology [J].
Lefkowitch, Jay H. .
SEMINARS IN DIAGNOSTIC PATHOLOGY, 2006, 23 (3-4) :190-198