Approaches and methods in gene therapy for kidney disease

Journal of Pharmacological and Toxicological Methods

Volumn 50, Issue 1, 2004, Pages 13-24

  Van Der Wouden, Els A ^a   Sandovici, Maria ^a   Henning, Robert H ^a   De Zeeuw, Dick ^a   Deelman, Leo E ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

Author keywords

Dog; Gene therapy; Human; Kidney; Methods; Mouse; Pig; Rabbit; Rat; Review

Indexed keywords

ADENOVIRUS VECTOR; ANTISENSE OLIGODEOXYNUCLEOTIDE; BETA GALACTOSIDASE; CANCER GROWTH FACTOR; CYTOKINE; CYTOTOXIC T LYMPHOCYTE ANTIGEN 4; GREEN FLUORESCENT PROTEIN; INTERLEUKIN 10; INTERLEUKIN 12; INTERLEUKIN 4; LENTIVIRUS VECTOR; LIPOPOLYSACCHARIDE; LIPOSOME; LUCIFERASE; PLASMID DNA; PROTEIN BCL 2; RETROVIRUS VECTOR; SCATTER FACTOR; SMAD7 PROTEIN; TUMOR NECROSIS FACTOR;

ADENOVIRUS; BLOOD VESSEL; BONE MARROW CELL; CELL TYPE; COXSACKIE VIRUS; DENDRITIC CELL; ELECTROPORATION; EPITHELIUM CELL; EPSTEIN BARR VIRUS; GENE DELIVERY SYSTEM; GENE EXPRESSION; GENE TARGETING; GENE THERAPY; GENE TRANSFER; GENETIC TRANSFECTION; GLOMERULUS; GRAFT REJECTION; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS 1; INFLAMMATION; INJECTION SITE; KIDNEY DISEASE; KIDNEY FIBROSIS; KIDNEY GRAFT; KIDNEY PARENCHYMA; KIDNEY TRANSPLANTATION; KIDNEY VEIN; LENTIVIRINAE; LEYDIG CELL; LYMPHOCYTE; MACROPHAGE; MESANGIUM CELL; MOLONEY LEUKEMIA ONCOVIRUS; MONOCYTE; NEPHRITIS; NONHUMAN; NONVIRAL GENE DELIVERY SYSTEM; PARAINFLUENZA VIRUS; PLASMID; RENAL ARTERY; RETROVIRUS; REVIEW; SIMIAN IMMUNODEFICIENCY VIRUS; T LYMPHOCYTE; URETER; VIRAL GENE DELIVERY SYSTEM;

ADENOVIRIDAE; CANIS FAMILIARIS; ORYCTOLAGUS CUNICULUS; SUS SCROFA;

EID: 3042689400     PISSN: 10568719     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vascn.2004.03.004     Document Type: Article

References (69)

1. Azuma H., Tomita N., Kaneda Y., Koike H., Ogihara T., Katsuoka Y., Morishita R. Transfection of NFkappaB-decoy oligodeoxynucleotides using efficient ultrasound-mediated gene transfer into donor kidneys prolonged survival of rat renal allografts. Gene Therapy. 10:2003;415-425
2. Barnett B.G., Crews C.J., Douglas J.T. Targeted adenoviral vectors. Biochimica Biophysica Acta. 1575:2002;1-14
3. Benigni A., Tomasoni S., Lutz J., Amuchastegui S., Capogrossi M.C., Remuzzi G. Nonviral and viral gene transfer to the kidney in the context of transplantation. Nephron. 85:2000;307-316
4. Boletta A., Benigni A., Lutz J., Remuzzi G., Soria M.R., Monaco L. Nonviral gene delivery to the rat kidney with polyethylenimine. Human Gene Therapy. 8:1997;1243-1251
5. Bosch R.J., Woolf A.S., Fine L.G. Gene transfer into the mammalian kidney: Direct retrovirus-transduction of regenerating tubular epithelial cells. Experimental Nephrology. 1:1993;49-54
6. Brasile L., Stubenitsky B.M., Booster M.H., Arenada D., Haisch C., Kootstra G. Transfection and transgene expression in a human kidney during ex vivo warm perfusion. Transplantation Proceedings. 34:2002;2624
7. Cassivi S.D., Liu M., Boehler A., Pierre A., Tanswell A.K., O'Brodovich H., Mullen J.B., Slutsky A.S., Keshavjee S. Transplant immunosuppression increases and prolongs transgene expression following adenoviral-mediated transfection of rat lungs. Journal of Heart and Lung Transplantation. 19:2000;984-994
8. Chen S., Agarwal A., Glushakova O.Y., Jorgensen M.S., Salgar S.K., Poirier A., Flotte T.R., Croker B.P., Madsen K.M., Atkinson M.A., Hauswirth W.W., Berns K.I., Tisher C.C. Gene delivery in renal tubular epithelial cells using recombinant adeno-associated viral vectors. Journal of the American Society of Nephrology. 14:2003;947-958
9. Chetboul V., Klonjkowski B., Lefebvre H.P., Desvaux D., Laroute V., Rosenberg D., Maurey C., Crespeau F., Adam M., Adnot S., Eloit M., Pouchelon J.L. Short-term efficiency and safety of gene delivery into canine kidneys. Nephrology Dialysis Transplantation. 16:2001;608-614
10. Dragun D., Tullius S.G., Park J.K., Maasch C., Lukitsch I., Lippoldt A., Gross V., Luft F.C., Haller H. ICAM-1 antisense oligodeoxynucleotides prevent reperfusion injury and enhance immediate graft function in renal transplantation. Kidney International. 54:1998;590-602
11. Gorczynski R.M., Bransom J., Cattral M., Huang X., Lei J., Xiaorong L., Min W.P., Wan Y., Gauldie J. Synergy in induction of increased renal allograft survival after portal vein infusion of dendritic cells transduced to express TGFbeta and IL-10, along with administration of CHO cells expressing the regulatory molecule OX-2. Clinical Immunology. 95:2000;182-189
12. Gusella G.L., Fedorova E., Hanss B., Marras D., Klotman M.E., Klotman P.E. Lentiviral gene transduction of kidney. Human Gene Therapy. 13:2002;407-414
13. Haas M., Moolenaar F., Meijer D.K., de Zeeuw D. Specific drug delivery to the kidney. Cardiovascular Drugs and Therapy. 16:2002;489-496
14. Hammer M.H., Flugel A., Seifert M., Lehmann M., Brandt C., Volk H.D., Ritter T. Potential of allospecific gene-engineered T cells in transplantation gene therapy: Specific T cell activation determines transgene expression in vitro and in vivo. Human Gene Therapy. 11:2000;1303-1311
15. Hammer M.H., Schroder G., Risch K., Flugel A., Volk H.D., Lehmann M., Ritter T. Antigen-dependent transgene expression in kidney transplantation: A novel approach using gene-engineered T lymphocytes. Journal of the American Society of Nephrology. 13:2002;511-518
16. Heikkila P., Parpala T., Lukkarinen O., Weber M., Tryggvason K. Adenovirus-mediated gene transfer into kidney glomeruli using an ex vivo and in vivo kidney perfusion system - first steps towards gene therapy of Alport syndrome. Gene Therapy. 3:1996;21-27
17. Imai E., Isaka Y. Strategies of gene transfer to the kidney. Kidney International. 53:1998;264-272
18. Isaka Y., Yamada K., Imai E., Tsujie M., Nakamura H., Yakabatake Y., Mizui T., Tanaka T., Utsugi R., Hori M., Takahara S. Electroporation mediated HGF gene transfection for preserving graft survival. Journal of the American Society of Nephrology. 13:2002;126A
19. Kalderon D., Roberts B.L., Richardson W.D., Smith A.E. A short amino acid sequence able to specify nuclear location. Cell. 39:1984;499-509
20. Kato H., Ritter T., Ke B., Murakami M., Kusano M., Busuttil R.W., Kupiec-Weglinski J.W. Adenovirus-mediated gene transfer of IL-4 prolongs rat renal allograft survival and inhibits the p21(ras)-activation pathway. Transplantation Proceedings. 32:2000;245-246
21. Kita J., Kobayashi E., Hishinuma A., Kaneda Y. Genetic modification of cold-preserved renal grafts using HSP70 or bcl-2 HVJ-liposome method. Transplant Immunology. 11:2003;7-14
22. Kitamura M., Burton S., Yokoo T., Fine L.G. Gene delivery into the renal glomerulus by transfer of genetically engineered, autologous mesangial cells. Experimental Nephrology. 4:1996;56-59
23. Kitamura M., Taylor S., Unwin R., Burton S., Shimizu F., Fine L.G. Gene transfer into the rat renal glomerulus via a mesangial cell vector: Site-specific delivery, in situ amplification, and sustained expression of an exogenous gene in vivo. Journal of Clinical Investigation. 94:1994;497-505
24. Kluth D.C., Erwig L.P., Pearce W.P., Rees A.J. Gene transfer into inflamed glomeruli using macrophages transfected with adenovirus. Gene Therapy. 7:2000;263-270
25. Kuemmerle N.B., Lin P.S., Krieg R.J. Jr., Lin K.C., Ward K.P., Chan J.C. Gene expression after intrarenal injection of plasmid DNA in the rat. Pediatric Nephrology. 14:2000;152-157
26. Lai L.W., Chan D.M., Erickson R.P., Hsu S.J., Lien Y.H. Correction of renal tubular acidosis in carbonic anhydrase II-deficient mice with gene therapy. Journal of Clinical Investigation. 101:1998;1320-1325
27. Lai L.W., Moeckel G.W., Lien Y.H. Kidney-targeted liposome-mediated gene transfer in mice. Gene Therapy. 4:1997;426-431
28. Lan H.Y., Mu W., Tomita N., Huang X.R., Li J.H., Zhu H.J., Morishita R., Johnson R.J. Inhibition of renal fibrosis by gene transfer of inducible Smad7 using ultrasound-microbubble system in rat UUO model. Journal of the American Society of Nephrology. 14:2003;1535-1548
29. Laverman G.D., de Zeeuw D., Navis G. Between-patient differences in the renal response to renin-angiotensin system intervention: Clue to optimising renoprotective therapy? Journal of the Renin-Angiotensin-Aldosterone System. 3:2002;205-213
30. Lipkowitz M.S., Hanss B., Tulchin N., Wilson P.D., Langer J.C., Ross M.D., Kurtzman G.J., Klotman P.E., Klotman M.E. Transduction of renal cells in vitro and in vivo by adeno-associated virus gene therapy vectors. Journal of the American Society of Nephrology. 10:1999;108-115
31. Liu F., Song Y., Liu D. Hydrodynamics-based transfection in animals by systemic administration of plasmid DNA. Gene Therapy. 6:1999;1258-1266
32. Mah C., Byrne B.J., Flotte T.R. Virus-based gene delivery systems. Clinical Pharmacokinetics. 41:2002;901-911
33. Maruyama H., Higuchi N., Nishikawa Y., Hirahara H., Iino N., Kameda S., Kawachi H., Yaoita E., Gejyo F., Miyazaki J. Kidney-targeted naked DNA transfer by retrograde renal vein injection in rats. Human Gene Therapy. 13:2002;455-468
34. McDonald G.A., Zhu G., Li Y., Kovesdi I., Wickham T.J., Sukhatme V.P. Efficient adenoviral gene transfer to kidney cortical vasculature utilizing a fiber modified vector. Journal of Gene Medicine. 1:1999;103-110
35. Morelli A.E., Thomson A.W. Dendritic cells: Regulators of alloimmunity and opportunities for tolerance induction. Immunology Review. 196:2003;125-146
36. Moullier P., Friedlander G., Calise D., Ronco P., Perricaudet M., Ferry N. Adenoviral-mediated gene transfer to renal tubular cells in vivo. Kidney International. 45:1994;1220-1225
37. Nahman N.S., Sferra T.J., Kronenberger J., Urban K.E., Troike A.E., Johnson A., Holycross B.J., Nuovo G.J., Sedmak D.D. Microsphere-adenoviral complexes target and transduce the glomerulus in vivo. Kidney International. 58:2000;1500-1510
38. Naito T., Yokoyama H., Moore K.J., Dranoff G., Mulligan R.C., Kelley V.R. Macrophage growth factors introduced into the kidney initiate renal injury. Molecular Medicine. 2:1996;297-312
39. Nakamura H., Isaka Y., Tsujie M., Rupprecht H.D., Akagi Y., Ueda N., Imai E., Hori M. Introduction of DNA enzyme for Egr-1 into tubulointerstitial fibroblasts by electroporation reduced interstitial alpha-smooth muscle actin expression and fibrosis in unilateral ureteral obstruction (UUO) rats. Gene Therapy. 9:2002;495-502
40. Ortiz P.A., Hong N.J., Plato C.F., Varela M., Garvin J.L. An in vivo method for adenovirus-mediated transduction of thick ascending limbs. Kidney International. 63:2003;1141-1149
41. Parpala-Sparman T., Lukkarinen O., Heikkila P., Tryggvason K. A novel surgical organ perfusion method for effective ex vivo and in vivo gene transfer into renal glomerular cells. Urology Research. 27:1999;97-102
42. Pellegrini C., O'Brien T., Jeppsson A., Fitzpatrick L.A., Yap J., Tazelaar H.D., McGregor C.G. Influence of temperature on adenovirus-mediated gene transfer. European Journal of Cardiothoracic Surgery. 13:1998;599-603
43. Rabb H., Barroso-Vicens E., Adams R., Pow-Sang J., Ramirez G. Alpha-V/beta-3 and alpha-V/beta-5 integrin distribution in neoplastic kidney. American Journal of Nephrology. 16:1996;402-408
44. Reddy P.S., Sakhuja K., Ganesh S., Yang L., Kayda D., Brann T., Pattison S., Golightly D., Idamakanti N., Pinkstaff A., Kaloss M., Barjot C., Chamberlain J.S., Kaleko M., Connelly S. Sustained human factor VIII expression in hemophilia A mice following systemic delivery of a gutless adenoviral vector. Molecular Therapeutics. 5:2002;63-73
45. Rha S.H., Kim S.E., Park B.H., Hwang T.H., Bae H.R., An W.S., Jung S.I., Kim K.H. Adenovirus-mediated gene transfer to rabbit renal glomeruli via percutaneous arterial catheterization. Journal of the American Society of Nephrology. 13:2002;128A
46. Schmidt-Wolf G.D., Schmidt-Wolf I.G. Non-viral and hybrid vectors in human gene therapy: An update. Trends in Molecular Medicine. 9:2003;67-72
47. Sonntag K.C., Emery D.W., Yasumoto A., Haller G., Germana S., Sablinski T., Shimizu A., Yamada K., Shimada H., Arn S., Sachs D.H., LeGuern C. Tolerance to solid organ transplants through transfer of MHC class II genes. Journal of Clinical Investigation. 107:2001;65-71
48. Takase O., Hirahashi J., Takayanagi A., Chikaraishi A., Marumo T., Ozawa Y., Hayashi M., Shimizu N., Saruta T. Gene transfer of truncated IkappaBalpha prevents tubulointerstitial injury. Kidney International. 63:2003;501-513
49. Taniyama Y., Tachibana K., Hiraoka K., Aoki M., Yamamoto S., Matsumoto K., Nakamura T., Ogihara T., Kaneda Y., Morishita R. Development of safe and efficient novel nonviral gene transfer using ultrasound: Enhancement of transfection efficiency of naked plasmid DNA in skeletal muscle. Gene Therapy. 9:2002;372-380
50. Terada Y., Hanada S., Nakao A., Kuwahara M., Sasaki S., Marumo F. Gene transfer of Smad7 using electroporation of adenovirus prevents renal fibrosis in post-obstructed kidney. Kidney International. 61(Suppl. 1):2002;94-98
51. Tomasoni S., Azzollini N., Casiraghi F., Capogrossi M.C., Remuzzi G., Benigni A. CTLA4Ig gene transfer prolongs survival and induces donor-specific tolerance in a rat renal allograft. Journal of the American Society of Nephrology. 11:2000;747-752
52. Tomita N., Higaki J., Morishita R., Kato K., Mikami H., Kaneda Y., Ogihara T. Direct in vivo gene introduction into rat kidney. Biochemical and Biophysical Research Communications. 186:1992;129-134
53. Tomko R.P., Xu R., Philipson L. HCAR and MCAR: The human and mouse cellular receptors for subgroup C adenoviruses and group B coxsackieviruses. Proceedings of the National Academy of Sciences of the United States of America. 94:1997;3352-3356
54. Tsujie M., Isaka Y., Ando Y., Akagi Y., Kaneda Y., Ueda N., Imai E., Hori M. Gene transfer targeting interstitial fibroblasts by the artificial viral envelope-type hemagglutinating virus of Japan liposome method. Kidney International. 57:2000;1973-1980
55. Tsujie M., Isaka Y., Nakamura H., Imai E., Hori M. Electroporation- mediated gene transfer that targets glomeruli. Journal of the American Society of Nephrology. 12:2001;949-954
56. Tsujie M., Isaka Y., Nakamura H., Kaneda Y., Imai E., Hori M. Prolonged transgene expression in glomeruli using an EBV replicon vector system combined with HVJ liposomes. Kidney International. 59:2001;1390-1396
57. Verkman A.S., Yang B. Aquaporin gene delivery to kidney. Kidney International. 61(Suppl. 1):2002;120-124
58. Vos I.H., Govers R., Grone H.J., Kleij L., Schurink M., De Weger R.A., Goldschmeding R., Rabelink T.J. NFkappaB decoy oligodeoxynucleotides reduce monocyte infiltration in renal allografts. FASEB Journal. 14:2000;815-822
59. Weiss D.J., Liggitt D., Clark J.G. Histochemical discrimination of endogenous mammalian beta-galactosidase activity from that resulting from lac-Z gene expression. Histochemical Journal. 31:1999;231-236
60. Woolf A.S., Palmer S.J., Snow M.L., Fine L.G. Creation of a functioning chimeric mammalian kidney. Kidney International. 38:1990;991-997
61. Yamagishi H., Yokoo T., Imasawa T., Mitarai T., Kawamura T., Utsunomiya Y. Genetically modified bone marrow-derived vehicle cells site specifically deliver an anti-inflammatory cytokine to inflamed interstitium of obstructive nephropathy. Journal of Immunology. 166:2001;609-616
62. Yang J., Reutzel-Selke A., Steier C., Jurisch A., Tullius S.G., Sawitzki B., Kolls J., Volk H.D., Ritter T. Targeting of macrophage activity by adenovirus-mediated intragraft overexpression of TNFRp55-Ig, IL-12p40, and vIL-10 ameliorates adenovirus-mediated chronic graft injury, whereas stimulation of macrophages by overexpression of IFN-gamma accelerates chronic graft injury in a rat renal allograft model. Journal of the American Society of Nephrology. 14:2003;214-225
63. Ye X., Liu X., Li Z., Ray P.E. Efficient gene transfer to rat renal glomeruli with recombinant adenoviral vectors. Human Gene Therapy. 12:2001;141-148
64. Yokoo T., Utsunomiya Y., Ohashi T., Imasawa T., Kogure T., Futagawa Y., Kawamura T., Eto Y., Hosoya T. Inflamed site-specific gene delivery using bone marrow-derived CD11b+CD18+ vehicle cells in mice. Human Gene Therapy. 9:1998;1731-1738
65. Yoo J.J., Soker S., Lin L.F., Mehegan K., Guthrie P.D., Atala A. Direct in vivo gene transfer to urological organs. Journal of Urology. 162:1999;1115-1118
66. Young D.C., Kingsley S.D., Ryan K.A., Dutko F.J. Selective inactivation of eukaryotic beta-galactosidase in assays for inhibitors of HIV-1 TAT using bacterial beta-galactosidase as a reporter enzyme. Analytical Biochemistry. 215:1993;24-30
67. Zeigler S.T., Kerby J.D., Curiel D.T., Diethelm A.G., Thompson J.A. Molecular conjugate-mediated gene transfer into isolated human kidneys. Transplantation. 61:1996;812-817
68. Zhu G., Nicolson A.G., Cowley B.D., Rosen S., Sukhatme V.P. In vivo adenovirus-mediated gene transfer into normal and cystic rat kidneys. Gene Therapy. 3:1996;298-304
69. Zou L., Zhou H., Pastore L., Yang K. Prolonged transgene expression mediated by a helper-dependent adenoviral vector (hdAd) in the central nervous system. Molecular Therapeutics. 2:2000;105-113