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Arterial Gene Transfer

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Biology of the Arterial Wall

Part of the book series: Basic Science for the Cardiologist ((BASC,volume 1))

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Abstract

Atherosclerosis and its complications represent the first cause of mortality and morbidity in the western world. Major advances have been made in the treatment and prevention of symptomatic atherosclerosis. Improved understanding of the pathophysiology of atherosclerosis and its complications [1], as well as spectacular advances in the molecular biology of the vascular wall [2] may open new perspectives for treatment based upon local delivery of genetic material designed to modify the atherosclerotic plaque at the molecular level [3]. Transfer of a functional gene into arterial wall cells, termed arterial gene therapy, may be used to replace or palliate a defective gene, or to express a protein with a therapeutic effect [4].

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References

  1. Ross R. The pathogenesis of atherosclerosis: a perspective for the 1990s. Nature. 1993;362:801–809.

    Article  PubMed  CAS  Google Scholar 

  2. Gibbons GH, Dzau VJ. Molecular therapies for vascular diseases. Science. 1996;272:689–693.

    Article  PubMed  CAS  Google Scholar 

  3. Nabel EG. Gene therapy for cardiovascular disease. Circulation. 1995;91:541–548.

    PubMed  CAS  Google Scholar 

  4. Isner JM, Feldman LJ. Gene therapy for arterial disease. Lancet. 1994;344:1653–4.

    Article  PubMed  CAS  Google Scholar 

  5. Riessen R, Rahimizadeh H, Takeshita S, Gal D, Barry JJ, Isner JM. Successful vascular gene transfer using a hydrogel coated balloon angioplasty catheter. Hum Gene Ther. 1993;4:749–758.

    PubMed  CAS  Google Scholar 

  6. Mulligan RC. The basic science of gene therapy. Science. 1993;260:926–932.

    Article  PubMed  CAS  Google Scholar 

  7. Nabel EG, Plautz G, Nabel GJ. Site-specific gene expression in vivo by direct gene transfer into the arterial wall. Science. 1990;249:1285–1288.

    Article  PubMed  CAS  Google Scholar 

  8. Berkner KL. Expression of heterologous sequences in adenoviral vectors. Curr. Top. Microbiol. Immunol. 1992;158:39–66.

    PubMed  CAS  Google Scholar 

  9. Steg PG, Feldman LJ, Scoazec JY, Tahlil O, Barry JJ, Boulechfar S, Ragot T, Isner JM, Perricaudet M. Arterial gene transfer to rabbit endothelial and smooth muscle cells using percutaneous delivery of an adenoviral vector. Circulation. 1994;90:1648–56.

    PubMed  CAS  Google Scholar 

  10. Tripathy SK, Black HB, Goldwasser E, Leiden JM. Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors. Nature Med. 1996;2:545–550.

    Article  PubMed  CAS  Google Scholar 

  11. Yang Y, Nunes FA, Berencsi K, Furth EE, Gönczöl E, Wilson JM. Cellular immunity to viral antigens limits El-deleted adenoviruses for gene therapy. Proc Natl Acad Sci USA. 1994;91:4407–4411.

    Article  PubMed  CAS  Google Scholar 

  12. Schulick AH, Newman KD, Virmani R, Dichek DA. In vivo gene transfer into injured carotid arteries. Optimization and evaluation of acute toxicity. Circulation. 1995;91:2407–2414.

    PubMed  CAS  Google Scholar 

  13. Feldman LJ, Pastore CJ, Aubailly N, Kearney M, Chen D, Perricaudet M, Steg PG, Isner JM. Improved efficiency of arterial gene transfer by use of poloxamer 407 as a vehicle for adenoviral vectors. Gene Ther. 1997;4:189–98.

    Article  PubMed  CAS  Google Scholar 

  14. Newman KD, Dunn PF, Owens JW, Schulick AH, Virmani R, Sukhova G, Libby P, Dichek DA. Adenovirus-mediated gene transfer into normal rabbit arteries results in prolonged vascular cell activation, inflammation, and neointimal hyperplasia. J Clin Invest. 1995;96:2955–2965.

    Article  PubMed  CAS  Google Scholar 

  15. Van Ginkel F, Liu C, Simecka J, Dong J, Greenway T, Frizzel R, Kiyono H, McGhee J, Pascual D. Intratracheal gene delivery with adenoviral vector induces elevated systemic IgG and mucosal IgA antibodies to adenovirus and ß-galactosidase. Hum Gene Ther. 1995;6:895–903.

    PubMed  Google Scholar 

  16. Stratford-Perricaudet LD, Makeh I, Perricaudet M, Briand P. Widespread long-term gene transfer to mouse skeletal muscles and heart. J Clin Invest. 1992;90:626–630.

    PubMed  CAS  Google Scholar 

  17. Vilquin J-T, Guérette B, Kinoshita I, Roy B, Goulet M, Gravel C, Roy R, Tremblay JP. FK506 immunosuppression to control the immune reactions triggered by first-generation adenovirus-mediated gene transfer. Hum Gene Ther. 1995;6:1391–1401.

    PubMed  CAS  Google Scholar 

  18. Engelhardt JF, Ye X, Doranz B, Wilson JM. Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver. Proc Natl Acad Sci USA. 1994;91:6196–6200.

    Article  PubMed  CAS  Google Scholar 

  19. Yeh P, Dedieu J-F, Orsini C, Vigne E, Denefle P, Perricaudet P. Efficient dual transcomplementation of adenovirus El and E4 regions from a 293-derived cell line expressing a minimal E4 functional unit. J Virol. 1996;70:559–565.

    PubMed  CAS  Google Scholar 

  20. Wang Q, Finer MH. Second-generation adenovirus vectors. Nature Med. 1996;2:714–716.

    Article  PubMed  CAS  Google Scholar 

  21. Felgner PL, Ringold GM. Cationic liposome-mediated transfection. Nature. 1989;337:387–388.

    Article  PubMed  CAS  Google Scholar 

  22. Leclerc G, Gal D, Takeshita S, Nikol S, Weir L, Isner JM. Percutaneous arterial gene transfer in a rabbit model. Efficiency in normal and balloon-dilated atherosclerotic arteries. J Clin Invest. 1992;90:936–944.

    PubMed  CAS  Google Scholar 

  23. Michael SI, Curiel DT. Strategies to achieve targeted gene delivery via the receptor-mediated endocytosis pathway. Gene Therapy. 1994; 1:223–232.

    PubMed  CAS  Google Scholar 

  24. Morishita R, Gibbons G, Kaneda Y, Ogihara T, Dzau V. Novel and effective gene transfer technique for study of vascular renin angiotensin system. J Clin Invest. 1993;91:2580–2585.

    PubMed  CAS  Google Scholar 

  25. von der Leyen HE, Gibbons GH, Morishita R, Lewis NP, Zhang L, Nakajima M, Kaneda Y, Cooke JP, Dzau VJ. Gene therapy inhibiting neointimal vascular lesion: in vivo transfer of endothelial cell nitric oxide synthase gene. Proc Natl Acad Sci USA. 1995;92:1137–1141.

    Article  PubMed  Google Scholar 

  26. Morishita R, Gibbons GH, Ellison KE, Nakajima M, von der Leynen H, Zhang L, Kaneda Y, Ogihara T, Dzau VJ. Intimai hyperplasia after vascular injury is inhibited by antisense cdk 2 kinase oligonucleotides. J Clinlnvest. 1994;93:1458–1464.

    CAS  Google Scholar 

  27. Morishita R, Gibbons GH, Horiuchi M, Ellison KE, Nakajima M, Zhang L, Kaneda Y, Ogihara T, Dzau VJ. A gene therapy strategy using a transcription factor decoy of the E2F binding site inhibits smooth muscle proliferation in vivo. Proc Natl Acad Sci USA. 1995;92:5855–5859.

    Article  PubMed  CAS  Google Scholar 

  28. Riessen R, Isner JM. Prospects for site-specific delivery of pharmacologic and molecular therapies. J Am Coll Cardiol 1994;23:1234–1244.

    PubMed  CAS  Google Scholar 

  29. Tahlil O, Brami M, Feldman LJ, Branellec D, Steg PG. The Dispatch catheter as a delivery tool for arterial gene transfer. Cardiovasc Res. 1997;33:181–7.

    Article  PubMed  CAS  Google Scholar 

  30. Isner JM, Pieczek A, Schainfield R, Blair R, Haley L, Asahara T, Rosenfield K, Razvi S, Walsh K, Symes JF. Clinical evidence of angiogenesis after arterial gene transfer of phVEGF165 in patient with ischaemic limb. Lancet. 1996;348:370–374.

    Article  PubMed  CAS  Google Scholar 

  31. Wolinsky H, Thung SN. Use of a perforated balloon catheter to deliver concentrated heparin into the wall of the normal canine artery. J Am CollCardiol 1990;15:475–481.

    Article  CAS  Google Scholar 

  32. Lambert CR, Leone JE, Rowlands SM. Local drug delivery catheters: functional comparisson of porous and microporous designs. Cor Art Dis. 1993;4:469–475.

    CAS  Google Scholar 

  33. Feldman LJ, Steg PG, Zheng LP, Chen D, Kearney M, McGarr SE, Barry JJ, Dedieu JF, Perricaudet M, Isner JM. Low-efficiency of percutaneous adenovirus-mediated arterial gene transfer in the atherosclerotic rabbit. J Clin Invest. 1995;95:2662–71.

    PubMed  CAS  Google Scholar 

  34. Lincoff AM, Topol EJ, Ellis SG. Local drug delivery for the prevention of restenosis. Fact, fancy, and future. Circulation. 1994;90:2070–2084.

    PubMed  CAS  Google Scholar 

  35. Dichek DA, Neville RF, Zwiebel JA, Freeman SM, Leon MB, Anderson WF. Seeding of intravascular stents with genetically engineered endothelial cells. Circulation. 1989;80:1347–1353.

    PubMed  CAS  Google Scholar 

  36. Dev V, Zeng H, Forrester JS, Eigler N, Tian Y, Hickey AJ, Fishbein MC, Kupfer J, Litvak F. Microspheres for drug delivery to the arterial wall: a study of kinetics, toxicity, and effects of corticosteroid loaded microspheres. J Am Coll Cardiol. 1994, 23:19 A. Abstract.

    Google Scholar 

  37. Slepian MJ, Sawhney A, Pathak CP, Khosravi F, Roth L, Massia SP, Hubbell JA. In situ photo-polymerized thin hydrogel barriers applied following arterial injury reduce intimai thickening. J Am Coll Cardiol. 1994;23:473A. Abstract.

    Google Scholar 

  38. Indolfi C, Awedimento EV, Rapacciuolo A, Di Lorenzo E, Esposito G, Stabile E, Mele E, Giuliano P, Condorelli GL, Chiariello M. Inhibition of cellular ras prevents smooth muscle cell proliferation after vascular injury in vivo. Nature Med. 1995;1:541–545.

    Article  PubMed  CAS  Google Scholar 

  39. Simons M, Edelman ER, DeKeyser J-L, Langer R, Rosenberg RD. Antisense c-myb oligonucleotides inhibit intimai arterial smooth muscle cell accumulation in vivo. Nature. 1992;359:67–70.

    Article  PubMed  CAS  Google Scholar 

  40. Wolff JA, Malone RW, Williams P, Chong W, Acsadi G, Jani A, Feigner PL. Direct gene transfer into mouse muscle in vivo. Science. 1990;247:1465–1468.

    Article  PubMed  CAS  Google Scholar 

  41. French BA, Mazur W, Geske RS, Bolli R. Direct in vivo gene transfer into porcine myocardium using replication-deficient adenoviral vectors. Circulation. 1994;90:2414–2424.

    PubMed  CAS  Google Scholar 

  42. Barr E, Carroll J, Kalynych AM, Tripathy SK, Kozarsky K, Wilson JM. Efficient catheter-mediated gene transfer into the heart using replication-defective adenovirus. Gene Ther, 1994;1:51–58.

    PubMed  CAS  Google Scholar 

  43. Giordano FJ, Ping P, McKirnan MD, Nozaki S, DeMaria AN, Dillman WH, Mathieu-Costello O, Hammond HK. Intracoronary gene transfer of fibroblast growth factor-5 increases blood flow and contractile function in an ischemic region of the heart. Nature Med. 1996;2:534–539.

    Article  PubMed  CAS  Google Scholar 

  44. Logeart D, Hatem SN, Inamo J, Haddada H, Perricaudet M, Mercadier JJ. Increased efficiency of gene transfer to cardiac myocytes with recombinant adenovirus by altering the endothelial barrier permeability. Circulation. 1996;94(suppl I):1–590. Abstract.

    Google Scholar 

  45. Nabel EJ, Plautz G, Boyce DM, Stanley JC, Nabel GJ. Recombinant gene expression in vivo within endothelial cells of the arterial wall. Science. 1989;244:1342–1344.

    Article  PubMed  CAS  Google Scholar 

  46. Flugelman MY, Jaklitsch MT, Newman KD, Casscells W, Brathauer GL, Dichek DA. Low level in vivo gene transfer into the arterial wall through a perforated balloon catheter. Circulation. 1992;85:1110–1117.

    PubMed  CAS  Google Scholar 

  47. Lemarchand P, Jones M, Yamada I, Crystal RG. In vivo gene transfer and expression in normal uninjured blood vessels using replication-deficient recombinant adenovirus vectors. Circ Res. 1993;72:1132–1138.

    PubMed  CAS  Google Scholar 

  48. Schulick AH, Dong G, Newman KD, Virmani R, Dichek DA. Endothelium-specific in vivo gene transfer. Circ Res. 1995;77:475–485.

    PubMed  CAS  Google Scholar 

  49. Rome JJ, Shayani V, Flugelman MY, Newman KD, Farb A, Virmani R, Dichek DA. Anatomic barriers influence the distribution of in vivo gene transfer into the arterial wall. Modeling with microscopic tracer particles and verification with a recombinant adenoviral vector. Arterioscler Thromb. 1994;14:148–161.

    PubMed  CAS  Google Scholar 

  50. Maillard L, Ziol M, Tahlil O, Le Feuvre C, Feldman LJ, Branellec D, Bruneval P, Steg PG. Pre-treatment with elastase improves the efficiency of percutaneous adenovirus-mediated gene ransfer to the arterial media. Gene Ther. 1998. In press.

    Google Scholar 

  51. Bohl D, Naffakh N, Heard J-M. Long-term control of erythropoietin secretion by doxyxycline in mice transplanted with engineered primary myoblasts. Nature Med. 1997;3:299–305.

    Article  PubMed  CAS  Google Scholar 

  52. Nabel EJ, Yang Z, Liptay S, San H, Gordon D, Haudenschild CC, Nabel GJ. Recombinant platelet-derived growth factor B gene expression in porcine arteries induces intimai hyperplasia in vivo. J. Clin. Invest. 1993;91:1822–1829.

    PubMed  CAS  Google Scholar 

  53. Isner JM, Walsh K, Symes J, Pieczek A, Takeshita S, Lowry J, Rossow S, Rosenfield K, Weir L, Brogi E, Schainfeld R. Arterial gene therapy for therapeutic angiogenesis in patients with peripheral artery disease. Circulation. 1995;91:2687–2691.

    PubMed  CAS  Google Scholar 

  54. Lee JS, Feldman AM. Gene therapy for therapeutic myocardial angiogenesis: a promising synthesis of two emerging technologies. Nature Med. 1998;4:739–742.

    Article  PubMed  Google Scholar 

  55. Chen S-J, Wilson JM, Muller DWM. Adenovirus-mediated gene transfer of soluble vascular cell adhesion molecule to porcine interposition vein grafts. Circulation. 1994;89:1922–1928.

    PubMed  CAS  Google Scholar 

  56. Feldman LJ, Isner JM. Gene therapy for the vulnerable plaque. J Am Coll Cardiol 1995;26:826–35.

    Article  PubMed  CAS  Google Scholar 

  57. Lafont A, Guérot C, Lemarchand P. Prospects for gene therapy in cardiovascular disease. Eur Heart J. 1996;17:1312–1317.

    PubMed  CAS  Google Scholar 

  58. Clowes AW, Reidy MA, Clowes MM. Mechanisms of stenosis after arterial injury. Lab Invest. 1983;49:208–215.

    PubMed  CAS  Google Scholar 

  59. Feldman LJ, Tahlil O, Steg PG. Perspectives of arterial gene therapy for the prevention of restenosis. Cardiovasc Res. 1996;32:194–207.

    Article  PubMed  CAS  Google Scholar 

  60. Lafont A, Guzman LA, Whitlow PL, Goormastic M, Cornhill JF, Chisolm GM. Restenosis after experimental angioplasty. Intimai, medial, and adventitial changes associated with constrictive remodeling. CircRes. 1995;76:996–1002.

    CAS  Google Scholar 

  61. Mintz GS, Popma JJ, Pichard AD, Kent KM, Satler LF, Wong SC, Hong MK, Kovach JA, Leon MB. Arterial remodeling after coronary angioplasty. A serial intravascular ultrasound study. Circulation. 1996;94:35–43.

    PubMed  CAS  Google Scholar 

  62. Shi Y, Pieniek M, Fard A, O’Brien J, Mannion JD, Zalewski A. Adventitial remodeling after coronary arterial injury. Circulation. 1996;93:340–348.

    PubMed  CAS  Google Scholar 

  63. Hoffmann R, S MG, Dussaillant GR, Popma JJ, Pichard AD, Satler LF, Kent KM, Griffin J, Leon MB. Patterns and mechanisms of in-stent restenosis. A serial intravascular ultrasound study. Circulation. 1996;94:1247–1254.

    PubMed  CAS  Google Scholar 

  64. Lafont A, Guerot C, Lemarchand P. Which gene for which restenosis? Lancet. 1995;346:1442–1443.

    Article  PubMed  CAS  Google Scholar 

  65. Van Belle E, Maillard L, Rivard A, Fabre JE, Couffinhal T, Kearney M, Branellec D, Feldman LF, Walsh K, Isner JM. Effects of poloxamer 407 on transfection time and percutaneous adenovirus-mediated gene transfer in native and stented vessels. Hum Gene Ther. 1998;9:1013–1024.

    Article  PubMed  Google Scholar 

  66. Baumgartner I, Pieczek AM, Blair R, Manor O, Walsh K, Isner JM. Evidence of therapeutic angiogenesis in patients with critical limb ischemia after intramuscular phVEGF165 gene transfer. Circulation. 1997;96:1–32. Abstract.

    Google Scholar 

  67. Schaper W, Ito WD. Molecular mechanisms of coronary collateral vessel growth. Circ Res. 1996;79:911–919.

    PubMed  CAS  Google Scholar 

  68. Tsurumi Y, Takeshita S, Chen D, Kearney M, Rossow ST, Passeri J, Horowitz JR, Symes JF, Isner JM. Direct intramuscular gene transfer of naked DNA encoding vascular endothelial growth factor augments collateral development and tissue perfusion. Circulation. 1996;94:3281–3290.

    PubMed  CAS  Google Scholar 

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© 1999 Kluwer Academic Publishers

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Feldman, L.J., Steg, P.G. (1999). Arterial Gene Transfer. In: Levy, B.I., Tedgui, A. (eds) Biology of the Arterial Wall. Basic Science for the Cardiologist, vol 1. Springer, Boston, MA. https://doi.org/10.1007/978-0-585-38146-6_13

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  • DOI: https://doi.org/10.1007/978-0-585-38146-6_13

  • Publisher Name: Springer, Boston, MA

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