Minimally invasive and selective hydrodynamic gene therapy of liver segments in the pig and human (original) (raw)
- Original Article
- Published: 08 February 2008
- P Bachellier1,2,
- J C Weber1,2,
- M Greget2,
- D Jaeck2,
- D Zacharoulis3,
- C Rountas3,
- S Helmy1,4,
- A Helmy4,
- M Al-Waracky4,
- H Salama4,
- L Jiao1,
- J Nicholls1,
- A J Davies1,
- N Levicar1,
- S Jensen1 &
- …
- N Habib1
Cancer Gene Therapy volume 15, pages 225–230 (2008)Cite this article
- 1449 Accesses
- 59 Citations
- 6 Altmetric
- Metrics details
Abstract
This paper highlights our experience of the transfer of hydrodynamic gene therapy (HGT) from the large animal, the pig, into clinical practice. The modification of balloon catheters and the development of a minimally invasive technique to allow selective isolation of liver segments for HGT in the large animal and human are described. Finally, our preliminary results from a phase I clinical study of HGT for thrombopoietin (TPO) in cirrhotic patients with thrombocytopenia are discussed. Based on these provisional data, minimally invasive selective HGT of liver segments appears to be technically safe, but further work is required to optimize the efficiency of gene transfer in order to achieve clinical benefit.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$259.00 per year
only $21.58 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Additional access options:
Similar content being viewed by others
References
- Budker V, Zhang G, Knechtel S, Wolff JA . Naked DNA delivered intraportally expresses efficiently in hepatocytes. Gene Therapy 1996; 13: 593–598.
Google Scholar - Liu F, Song YK, Liu D . Hydrodynamics-based transfection in animals by systemic administration of plasmid DNA. Gene Therapy 1999; 6: 1258–1266.
Article CAS Google Scholar - Zhang G, Gao X, Song YK, Vollmer R, Stolz DB, Gasiorowski JZ et al. Hydroboration as the mechanism of hydrodynamic delivery. Gene Therapy 2004; 11: 675–682.
Article CAS Google Scholar - Kobayashi N, Nishikawa M, Hirata K, Takakura Y . Hydrodynamics-based procedure involves transient hyperpermeability in the hepatic cellular membrane: implication of a nonspecific process in efficient intracellular gene delivery. J Gene Med 2004; 6: 584–592.
Article CAS Google Scholar - Andrianaivo F, Lecocq M, Wattiaux-De Coninck S, Wattiaux R, Jadot M . Hydrodynamics-based transfection of the liver: entrance into hepatocytes of DNA that causes expression takes place very early after injection. J Gene Med 2004; 6: 877–883.
Article CAS Google Scholar - Crespo A, Peydro A, Dasi F, Benet M, Calvete JJ, Revert F, Alino SF . Hydrodynamic liver gene transfer mechanism involves transient sinusoidal blood stasis and massive hepatocyte endocytic vesicles. Gene Therapy 2005; 12: 927–937.
Article CAS Google Scholar - Miao CH, Thompson AR, Loeb K, Ye X . Long term transgene and therapeutic level hepatic gene expression of human factor IX after naked plasmid transfer in vivo. Mol Ther 2001; 3: 947–957.
Article CAS Google Scholar - Eastman SJ, Baskin KM, Hodges BL, Chu O, Gates A, Dreusike R et al. Development of catheter-based procedures for transducing the isolated rabbit liver with plasmid DNA. Hum Gene Ther 2002; 13: 2065–2077.
Article CAS Google Scholar - Alino SF, Herrero MF, Noguera I, Dasi F, Sanchez M . Pig liver gene therapy by noninvasive interventionist catheterism. Gene Therapy 2007; 14: 334–343.
Article CAS Google Scholar - Yoshino H, Hashizume K, Kobayashi E . Naked plasmid DNA transfer to the porcine liver using rapid injection with large volume. Gene Therapy 2006; 13: 1696–1702.
Article CAS Google Scholar - Habib N, Havlik R, Jiao L, Kiri A, Jensen S, Nicholls J et al. Combination of Optison™ with ultrasound and electroporation increases albumin and thrombopoietin transgene expression whilst elongation factor promoter prolongs its duration. Gene Ther Mol Biol 2004; 8: 1–7.
Google Scholar
Acknowledgements
This work was generously supported by the Pedersen Family Charitable Foundation and InvivoGen Inc.
Author information
Authors and Affiliations
- Faculty of Medicine, Imperial College London, London, UK
S E Khorsandi, P Bachellier, J C Weber, S Helmy, L Jiao, J Nicholls, A J Davies, N Levicar, S Jensen & N Habib - Foundation Transplantation, Strasbourg, Hôspital Hautpierre, Strasbourg, France
P Bachellier, J C Weber, M Greget & D Jaeck - Larissa University School of Medicine, Larissa, Greece
D Zacharoulis & C Rountas - Faculty of Medicine, Cairo University, Cairo, Egypt
S Helmy, A Helmy, M Al-Waracky & H Salama
Authors
- S E Khorsandi
You can also search for this author inPubMed Google Scholar - P Bachellier
You can also search for this author inPubMed Google Scholar - J C Weber
You can also search for this author inPubMed Google Scholar - M Greget
You can also search for this author inPubMed Google Scholar - D Jaeck
You can also search for this author inPubMed Google Scholar - D Zacharoulis
You can also search for this author inPubMed Google Scholar - C Rountas
You can also search for this author inPubMed Google Scholar - S Helmy
You can also search for this author inPubMed Google Scholar - A Helmy
You can also search for this author inPubMed Google Scholar - M Al-Waracky
You can also search for this author inPubMed Google Scholar - H Salama
You can also search for this author inPubMed Google Scholar - L Jiao
You can also search for this author inPubMed Google Scholar - J Nicholls
You can also search for this author inPubMed Google Scholar - A J Davies
You can also search for this author inPubMed Google Scholar - N Levicar
You can also search for this author inPubMed Google Scholar - S Jensen
You can also search for this author inPubMed Google Scholar - N Habib
You can also search for this author inPubMed Google Scholar
Corresponding author
Correspondence toN Habib.
Rights and permissions
About this article
Cite this article
Khorsandi, S., Bachellier, P., Weber, J. et al. Minimally invasive and selective hydrodynamic gene therapy of liver segments in the pig and human.Cancer Gene Ther 15, 225–230 (2008). https://doi.org/10.1038/sj.cgt.7701119
- Received: 17 April 2007
- Revised: 01 November 2007
- Accepted: 24 November 2007
- Published: 08 February 2008
- Issue Date: April 2008
- DOI: https://doi.org/10.1038/sj.cgt.7701119