Gene transfer into kidney tubules and vasculature by adenoviral vectors

Experimental Nephrology

Volumn 5, Issue 2, 1997, Pages 137-143

  Sukhatme, Vikas P ^a   Cowley, Benjamin D ^b   Zhu, Guoming ^a  

^a BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

^b UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

Author keywords

galactosidase; adenovirus; gene transfer; kidney; tubules; vasculature

Indexed keywords

BETA GALACTOSIDASE; VIRUS VECTOR;

ADENOVIRUS; GENE TRANSFER; HUMAN; KIDNEY BLOOD VESSEL; KIDNEY TUBULE; NONHUMAN; PRIORITY JOURNAL; REVIEW;

ADENOVIRIDAE; ANIMALS; BETA-GALACTOSIDASE; GENE THERAPY; GENE TRANSFER TECHNIQUES; GENES, REPORTER; GENETIC VECTORS; HUMANS; KIDNEY DISEASES; KIDNEY TUBULES;

EID: 0030963447     PISSN: 10187782     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (20)

1. Crystal RG: Transfer of genes to humans: Early lessons and obstacles to success. Science 1995; 270:404-410.
2. Hitt M, Bett AJ, Addison CL, Prevec L, Graham FL: Techniques for human adenovirus vector construction and characterization; in Adolph KW (ed): Viral Gene Techniques: Methods in Molecular Genetics. San Diego, Academic Press, 1995, vol 7, pp 13-30.
3. Engelhardt JF, Simon RH, Yang Y, Zepeda M, Weber-Pendleton S, Doranz B: Adenovirus-mediated transfer of the CFTR gene to lung of nonhuman primates: Biological efficacy study. Hum Gene Ther 1993;4:759-769.
4. Yang Y, Nunes FA, Berencsi K, Furth EE, Gonczol E, Wilson JM: Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy. Proc Natl Acad Sci USA 1994;91:4407-4411.
5. Dai Y, Schwartz EM, Gu D, Zhang WW, Sarvetnick NZ, Verma IM: Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: Tolerization of factor IX and vector antigen allows for long-term expression. Proc Natl Acad Sci USA 1995;92: 1401-1405.
6. 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.
7. Mitani K, Graham FL, Caskey CT, Kochanek S: Rescue, propagation, and partial purification of a helper virus-dependent adnenovirus vector. Proc Natl Acad Sci USA 1995;92: 3854-3858.
8. Kochanek S, Clemens PR, Mitani K, Chen H-H, Chan S, Caskey CT: A new adenoviral vector: Replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and β-galactosidase. Proc Natl Acad Sci USA 1996;93:7531-5736.
9. Vilquin J-T, Guerette B, Kinoshita I, Roy B, Goulet M, Gravel C: FK506 immunosuppression to control the immune reactions triggered by first-generation adenovirus-mediated gene transfer. Hum Gene Ther 1995;6:1391-1401.
10. DeMatteo RP, Markmann JF, Kozarsky KF, Barker CF, Raper SE: Prolongation of adenoviral transgene expression in mouse liver by T lymphocyte subset depletion. Gene Ther 1996; 3:4-12.
11. Kolls JK, Lei D, Odom G, Nelson S, Summer WR, Gerber MA: Use of transient CD4 lymphocyte depletion to prolong transgene expression of E1-deleted adenoviral vectors. Hum Gene Ther 1996;7:489-497.
12. Wiertz EJHJ, Jones TR, Sun L, Bogyo M, Geuze HJ, Ploegh HL: The human cytomegalovirus US11 gene product dislocates MHC class I heavy chains from the endoplasmic reticulum to the cytosol. Cell 1996;84:769-779.
13. Amin R, Wilmott R, Schwarz Y, Trapnell B, Stark J: Replication-deficient adenovirus induces expression of interleukin-8 by airway epithelial cell in vitro. Hum Gene Ther 1995;6: 145-153.
14. Michael SI, Hong JS, Curiel DT, Engler JA: Addition of a short peptide ligand to the adenovirus fiber protein. Gene Ther 1995;2:660-668.
15. Chang H, Katoh T, Noda M, Kanegae Y, Saito I, Asano S, Kurokawa K: Highly efficient adenovirus-mediated gene transfer into renal cells in culture. Kidney Int 1995;47:322-326.
16. Moullier P, Friedlander G, Calise D, Ronco P, Perricaudet M, Ferry N: Adenoviral-mediated gene transfer to renal tubular cells in vivo. Kidney Int 1994;45:1220-1225.
17. Zeigler ST, Kerby JD, Curiel DT, Diethelm AG, Thompson JA: Molecular conjugate-mediated gene transfer into isolated human kidneys. Transplantation 1996;61:812-817.
18. 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 step towards gene therapy of Alport syndrome. Gene Ther 1996;3:21-27.
19. Zhu G, Nicolson AG, Cowley BD Jr, Rosen S, Sukhatme VP: In vivo adenovirus-mediated gene transfer into normal and cystic rat kidneys. Gene Ther 1996;3:298-304.
20. Zhu G, Nicolson AG, Zheng X-X, Strom TB, Sukhatme VP: Adenovirus-mediated β-galactosidase gene delivery to the liver leads to protein deposition in kidney glomeruli. Kidney Int 1996, submitted.