Simultaneous infection with retroviruses pseudotyped with different envelope proteins bypasses viral receptor interference associated with colocalization of gp70 and target cells on fibronectin CH-296

Journal of Virology

Volumn 73, Issue 5, 1999, Pages 3960-3967

  MacNeill, Emily C ^a   Hanenberg, Helmut ^a,e   Pollok, Karen E ^a   Van Der Loo, Johannes C M ^a,b,f   Bierhuizen, Marti F A ^c   Wagemaker, Gerard ^c   Williams, David A ^a,b,d  

^a RILEY HOSPITAL FOR CHILDREN   (United States)

^b INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^d INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e HEINRICH HEINE UNIVERSITY   (Germany)

^f UNIV OF MINNESOTA HOSP AND CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ENVELOPE PROTEIN; FIBRONECTIN; VIRUS VECTOR;

ANIMAL CELL; ARTICLE; ERYTHROLEUKEMIA CELL; GENE TARGETING; HEMATOPOIETIC STEM CELL; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; RECEPTOR OCCUPANCY; RETROVIRUS; VIRUS EXPRESSION;

EID: 0032947284     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/jvi.73.5.3960-3967.1999     Document Type: Article

References (54)

1. Abonour, R., L. Einhorn, R. Hromas, M. J. Robertson, E. Srour, C. M. Traycoff, A. Bank, I. Kato, K. Asada, J. Croop, F. O. Smith, D. A. Williams, and K. Cornetta. 1998. High efficient MDR-1 gene transfer into humans using mobilized CD34+ cells transduced over recombinant fibronectin CH-296 fragment. Blood 92:690a.
2. Bierhuizen, M. F., Y. Westerman, T. P. Visser, W. Dimjati, A. W. Wognum, and G. Wagemaker. 1997. Enhanced green fluorescent protein as selectable marker of retroviral-mediated gene transfer in immature hematopoietic bone marrow cells. Blood 90:3304-3315.
3. Bodine, D. M., N. E. Seidel, M. S. Gale, A. W. Nienhuis, and D. Orlic. 1994. Efficient retrovirus transduction of mouse pluripotent hematopoietic stem cells mobilized into the peripheral blood by treatment with granulocyte colony-stimulating factor and stem cell factor. Blood 84:1482-1490.
4. Bodine, D. M., N. E. Seidel, and D. Orlic. 1996. Bone marrow collected 14 days after in vivo administration of granulocyte colony-stimulating factor and stem cell factor to mice has 10-fold more repopulating ability than untreated bone marrow. Blood 88:89-97.
5. Chien, M. L., J. L. Foster, J. L. Douglas, and J. V. Garcia. 1997. The amphotropic murine leukemia virus receptor gene encodes a 71-kilodalton protein that is induced by phosphate depletion. J. Virol. 71:4564-4570.
6. Conneally, E., C. J. Eaves, and R. K, Humphries. 1998. Efficient retroviral-mediated gene transfer to human cord blood stem cells with in vivo repopulating potential. Blood 91:3487-3493.
7. Correll, P. H., S. Colilla, H. P. G. Dave, and S. Karlsson. 1992. High levels of human glucocerebrosidase activity in macrophages of long-term reconstituted mice after retroviral infection of hematopoietic stem cells. Blood 80:331-336.
8. Crooks, G. M., and D. B. Kohn. 1993. Growth factors increase amphotropic retrovirus binding to human CD34+ bone marrow progenitor cells. Blood 82:3290-3297.
9. Deisseroth, A. B., Z. Zu, D. Claxton, E. G. Hanania, S. Fu, D. Ellerson, L. Goldberg, M. Thomas, K. Janicek, W. F. Anderson, J. Hester, M. Korbling, A. Durett, R. Moen, R. Berenson, S. Heimfeld, J. Hamer, L. Calvert, P. Tibbits, M. Talpaz, H. Kantarjian, R. Champlin, and C. Reading. 1994. Genetic marking shows that Ph+ cells present in autologous transplants of chronic myelogenous leukemia (CML) contribute to relapse after autologous bone marrow in CML. Blood 83:3068-3076.
10. Dunbar, C. E., M. Cottler-Fox, J. A. O'Shaughnessy, S. Doren, C. Carter, R. Berenson, S. Brown, R. C. Moen, J. Greenblatt, F. M. Stewart, S. F. Leitman, W. H. Wilson, K. Cowan, N. S. Young, and A. W. Nienhuis. 1995. Retrovirally marked CD34-enriched peripheral blood and bone marrow cells contribute to long-term engraftment after autologous transplantation. Blood 85:3048-3057.
11. Dunbar, C. E., N. E. Seidel, S. Doren, S. Sellers, A. P. Cline, M. E. Metzger, B. A. Agricola, R. E. Donahue, and D. M. Bodine. 1996. Improved retroviral gene transfer into murine and rhesus peripheral blood or bone marrow repopulating cells primed in vivo with stem cell factor and granulocyte colony-stimulating factor. Proc. Natl. Acad. Sci. USA 93:11871-11876.
12. Eipers, P. G., J. C. Krauss, B. O. Palsson, S. G. Emerson, R. F. Todd, and M. F. Clarke. 1995. Retroviral-mediated gene transfer in human bone marrow cells grown in continuous perfusion culture vessels. Blood 86:3754-3762.
13. Emmons, R. V. B., S. Doren, J. Zujewski, M. Cottler-Fox, C. S. Carter, K. Hines, J. A. O'Shaugnessy, S. F. Leitman, J. J. Greenblalt, K. Cowan, and C. E. Dunbar. 1997. Retroviral gene transduction of adult peripheral blood or marrow-derived CD34+ cells for six hours without growth factors or on autologous stroma does not improve marking efficiency assessed in vivo. Blood 89:4040-4046.
14. Evans, L. H., R. P. Morrison, F. G. Malik, J. Portis, and W. J. Britt. 1990. A neutralizable epitope common to the envelope glycoproteins of ecotropic, polytropic, xenotropic, and amphotropic murine leukemia viruses. J. Virol. 64:6176-6183.
15. Hanania, E. G., J. Kavanagh, G. Hortobagyi, R. E. Giles, R. Champlin, and A. B. Deisseroth. 1995. Recent advances in the application of gene therapy to human disease. Am. J. Med. 99:537-552.
16. Hanenberg, H., K. Hashino, H. Konishi, R. A. Hock, I. Kato, and D. A. Williams. 1997. Optimization of fibronectin-assisted retroviral gene transfer into human CD34+ hematopoietic cells. Hum. Gene Ther. 8:2193-2206.
17. Hanenberg, H., X. L. Xiao, D. Dilloo, K. Hashino, I. Kato, and D. A. Williams. 1996. Colocalization of retrovirus and target cells on specific fibronectin fragments increases genetic transduction of mammalian cells. Nat. Med. 2:876-882.
18. Hatzoglou, M., C. P. Hodgson, F. Mularo, and R. W. Hanson. 1990. Efficient packaging of a specific VL30 retroelement by psi 2 cells which produce MoMLV recombinant retroviruses. Hum. Gene Ther. 1:385-397.
19. Heifetz, A., W. Keenan, and A. D. Elbein. 1979. Mechanism of action of tunicamycin on the UDP-GlcNAc:dolichyl-phosphate GlcNAc-1-phosphate transferase. J. Biochem. 18:2186-2188.
20. Kadan, M. J., S. Sturm, W. F. Anderson, and M. A. Eglitis. 1992. Detection of receptor-specific murine leukemia virus binding to cells by immunofluorescence analysis. J. Virol. 66:2281-2287.
21. Kiem, H. P., S. Heyward, A. Winkler, J. Potter, J. M. Allen, A. D. Miller, and R. G. Andrews. 1997. Gene transfer into marrow repopulating cells: comparison between amphotropic and gibbon ape leukemia virus pseudotyped retroviral vectors in a competitive repopulation assay in baboons. Blood 90:4638-4645.
22. Kiem, H.-P., R. G. Andrews, J. Morris, L. Peterson, S. Heyward, J. M. Allen, J. E. J. Rasko. J. Potter, and D. A. Miller. 1998. Improved gene transfer into baboon marrow repopulating cells using recombinant human fibronectin fragment Ch-296 in combination with IL-6, stem cell factor, FLT-3 ligand, and megakaryocyte growth and development factor. Blood 92:1878-1886.
23. Kohn, D. B. 1997. Gene therapy for haematopoietic and lymphoid disorders. Clin. Exp. Immunol. 107:54-57.
24. Kohn, D. B., K. I. Weinberg, J. A. Nolta, L. N. Heiss, C. Lenarsky, G. M. Crooks, M. E. Hanley, G. Annett, J. S. Brooks, A. El-Khoureiy, K. Lawrence, S. Wells, R. C. Moen, J. Bastian, D. E. Williams-Herman, M. Elder, D. Wara, T. Bowen, M. S. Hershfield, C A. Mullen, R. M. Blaese, and R. Parkman. 1995. Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiency. Nat. Med. 1:1017-1023.
25. Kotani, H., P. B. I. Newton, S. Zhang, Y. L. Chiang, E. Otto, L. Weaver, R. M. Blaese, W. F. Anderson, and G. J. McGarrity. 1994. Improved methods of retroviral vector transduction and production for gene therapy. Hum. Gene Ther. 5:19-28.
26. Larochelle, A., J. Vormoor, H. Hanenberg, J. C. Y. Wang, M. Bhatia, T. Lapidot, T. Moritz, B. Murdoch, X. L. Xiao, I. Kato, D. A. Williams, and J. E. Dick. 1996. Identification of primitive human hematopoietic cells capable of repopulating NOD/SCID mouse bone marrow: implications for gene therapy. Nat. Med. 2:1329-1337.
27. Le Doux, J. M., J. R. Morgan, R. G. Snow, and M. L. Yarmush. 1996. Proteoglycans secreted by packaging cell lines inhibit retrovirus infection. J. Virol. 70:6468-6473.
28. Lombardi, S., C. Massi, E. Indino, C. La Rosa, P. Mazzetti, M. L. Falcone, P. Rovero, A. Fissi, O. Pieroni, P. Bandecchi, F. Esposito, F. Tozzini, M. Bendinelli, and C. Garzelli. 1996. Inhibition of feline immunodeficiency virus infection in vitro by envelope glycoprotein synthetic peptides. Virology 220:274-284.
29. Markowitz, D., S. Goff, and A. Bank. 1988. Construction and use of a safe and efficient amphotropic packaging cell line. Virology 167:400-406.
30. Marshall, E. 1995. Gene therapy's growing pains. Science 269:1050-1055.
31. Miller, A. D. 1996. Cell surface receptors for retroviruses and implications for gene transfer. Proc. Natl. Acad. Sci. USA 93:11407-11413.
32. Miller, A. D., and C. Buttimore. 1986. Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production. Mol. Cell. Biol. 6:2895-2902.
33. Miller, A. D., and F. Chen. 1996. Retrovirus packaging cells based on 10A1 murine leukemia virus for production of vectors that use multiple receptors for cell entry. J. Virol. 70:5564-5571.
34. Miller, A. D., J. V. Garcia, N. von Suhr, C. M. Lynch, C. Wilson, and M. V. Eiden. 1991. Construction and properties of retrovirus packaging cells based on gibbon ape leukemia virus. J. Virol. 65:2229-2224.
35. Miller, D. A. 1992. Human gene therapy comes of age. Nature 357:455-460.
36. Miller, D. G., M. A. Adam, and A. D. Miller. 1990. Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection. Mol. Cell. Biol. 10:4239-4242.
37. Miller, D. G., R. H. Edwards, and A. D. Miller. 1994. Cloning of the cellular receptor for amphotropic murine retroviruses reveals homology to that for gibbon ape leukemia virus. Proc. Natl. Acad. Sci. USA 91:78-82.
38. Moritz, T., P. Dutt, X. L. Xiao, D. Carstanjen, T. Vik, H. Hanenberg, and D. A. Williams. 1996. Fibronectin improves transduction of reconstituting hematopoietic stem cells by retroviral vectors: evidence of direct viral binding to chymotryptic carboxy-terminal fragments. Blood 88:855-862.
39. Moritz, T., V. P. Patel, and D. A. Williams. 1994. Bone marrow extracellular matrix molecules improve gene transfer into human hematopoietic cells via retroviral vectors. J. Clin. Investig. 93:1451-1457.
40. Moritz, T., and D. A. Williams. 1994. Gene transfer into the hematopoietic system: vectors and gene transfer protocols. Curr. Opin. Hematol. 1:423-428.
41. Orkin, S. H., and A. G. Motulsky. 7 December 1995, posting date. Report and recommendations of the panel to assess the NIH investment in research on gene therapy. [Online.] U.S. Department of Health and Human Services, National Institutes of Health, Bethesda, Md. www.nih.gov/news/panel-rep.html.
42. Orlic, D., L. J. Girard, S. M. Anderson, B. K. Do, N. E. Seidel, C. T. Jordan, and D. M. Bodine. 1997. Transduction efficiency of cell lines and hematopoietic stem cells correlates with retrovirus receptor mRNA levels. Stem Cells 15(Suppl.):23-29.
43. Orlic, D., L. J. Girard, S. M. Anderson, L. C. Pyle, M. C. Yoder, H. E. Broxmeyer, and D. M. Bodine. 1998. Identification of human and mouse hematopoietic stem cell populations expressing high levels of mRNA encoding retrovirus receptors. Blood 91:3247-3254.
44. Paul, R. W., D. Morris, B. W. Hess, J. Dunn, and R. W. Overell. 1993. Increased viral titers through concentration of viral harvests from retroviral packaging lines. Hum. Gene Ther. 4:609-615.
45. Pedersen, L., M. Van Zeijl, S. V. Johann, and B. O'Hara. 1997. Fungal phosphate transporter serves as a receptor backbone for gibbon ape leukemia virus. J. Virol. 71:7619-7622.
46. Pollok, K. E., H. Hanenberg, T. W. Noblitt, W. L. Schroeder, I. Kato. D. Emanuel, and D. A. Williams. 1998. High-efficiency gene transfer into normal and adenosine deaminase-deficient T-lymphocytes is mediated by transduction on recombinant fibronectin fragments. J. Virol. 72:4882-4892.
47. Rein, A., A. M. Schultz, J. P. Bader, and R. H. Bassin. 1982. Inhibitors of glycosylation reverse retroviral interference. Virology 119:185-192.
48. Rubin, H. 1960. A virus in chick embryos which induced resistance to in vitro infection by Rous sarcoma virus. Proc. Natl. Acad. Sci. USA 46:1105-1119.
49. Sabatino, D. E., B. Q. Do, L. C. Pyle, N. E. Seidel, L. J. Girard, S. K. Spratt, D. Orlic, and D. M. Bodine. 1997. Amphotropic or gibbon ape leukemia virus retrovirus binding and transduction correlates with the level of receptor mRNA in human hematopoietic cell lines. Blood Cells Mol. Dis. 23:422-433.
50. van Hennik, P. B., M. M. A. Verstegen, M. F. A. Bierhuizen, A. Limon, A. W. Wognum, J. A. Cancelas, J. Barquinero, R. E. Ploemacher, and G. Wagemaker. 1998. Highly efficient transduction of the green fluorescent protein gene in human umbilical cord blood stem cells capable of cobblestone formation in long-term cultures and multilineage engraftment of immunodeficient mice. Blood 92:4013-4022.
51. von Laer, D., S. Thomsen, B. Vogt, M. Donath, J. Kruppa, A. Rein, W. Ostertag, and C. Stocking. 1998. Entry of amphotropic and 10A1 pseudotyped murine retroviruses is restricted in hematopoietic stem cell lines. J. Virol. 72:1424-1430.
52. Walker, P. S., U. R. Hengge, M. C. Udey, I. Aksentijevich, and J. C. Vogel. 1996. Viral interference during simultaneous transduction with two independent helper-free retroviral vectors. Hum. Gene Ther. 7:1131-1138.
53. Wilson, C. A., and M. V. Eiden. 1991. Viral and cellular factors governing hamster cell infection by murine gibbon ape leukemia viruses. J. Virol. 65: 5975-5982.
54. Wilson, J. M., O. Danos, M. Grossman, D. H. Raulet, and R. C. Mulligan. 1990. Expression of human adenosine deaminase in mice reconstituted with retrovirus-transduced hematopoietic stem cells. Proc. Natl. Acad. Sci. USA 87:439-443.