메뉴 건너뛰기




Volumn 11, Issue 8, 1997, Pages 624-634

Adenoviral/retroviral vector chimeras: A novel strategy to achieve high- efficiency stable transduction in vivo

Author keywords

Adenoviral vector; Retrovirus; Transgene sequence; Vector chimera gene delivery

Indexed keywords

ADENOVIRUS; CHIMERA; EXPRESSION VECTOR; GENE TARGETING; GENE TECHNOLOGY; GENE THERAPY; GENE TRANSFER; GENETIC DISORDER; HUMAN; NONHUMAN; PRIORITY JOURNAL; RETROVIRUS; REVIEW; SIGNAL TRANSDUCTION;

EID: 0030806875     PISSN: 08926638     EISSN: None     Source Type: Journal    
DOI: 10.1096/fasebj.11.8.9240964     Document Type: Review
Times cited : (64)

References (111)
  • 1
    • 0021131380 scopus 로고
    • Prospects for human gene therapy
    • Anderson, W. F. (1984) Prospects for human gene therapy. Science 226, 401-409
    • (1984) Science , vol.226 , pp. 401-409
    • Anderson, W.F.1
  • 2
    • 0025279402 scopus 로고
    • Progress toward human gene therapy
    • Miller, A. D. (1990) Progress toward human gene therapy. Blood 76, 271-278
    • (1990) Blood , vol.76 , pp. 271-278
    • Miller, A.D.1
  • 5
    • 0026775132 scopus 로고
    • Concepts and strategies for human gene therapy
    • Roemer, K., and Friedmann, T. (1992) Concepts and strategies for human gene therapy. Ear. J. Biochem. 208, 211-225
    • (1992) Ear. J. Biochem. , vol.208 , pp. 211-225
    • Roemer, K.1    Friedmann, T.2
  • 7
    • 0027162409 scopus 로고
    • Direct gene transfer: Basic studies and human therapies
    • Nabel, E. G., and Nabel, G. J. (1993) Direct gene transfer: basic studies and human therapies. Thromb. Haemostasia 70, 202-203
    • (1993) Thromb. Haemostasia , vol.70 , pp. 202-203
    • Nabel, E.G.1    Nabel, G.J.2
  • 8
    • 0028825747 scopus 로고
    • Gene therapy for cystic fibrosis: Challenges and future directions
    • Wilson, J. M. (1995) Gene therapy for cystic fibrosis: Challenges and future directions. J. Clin. Invest. 96, 2547-2554
    • (1995) J. Clin. Invest. , vol.96 , pp. 2547-2554
    • Wilson, J.M.1
  • 9
    • 0030026531 scopus 로고    scopus 로고
    • Gene therapy for cystic fibrosis
    • Rosenfeld, M. A., and Collins, F. S. (1996) Gene therapy for cystic fibrosis. Chest 109, 241-252
    • (1996) Chest , vol.109 , pp. 241-252
    • Rosenfeld, M.A.1    Collins, F.S.2
  • 12
    • 0028965269 scopus 로고
    • Gene therapy approaches for cystic fibrosis
    • Coutelle, C. (1995) Gene therapy approaches for cystic fibrosis. Biologicals 23, 21-25
    • (1995) Biologicals , vol.23 , pp. 21-25
    • Coutelle, C.1
  • 14
    • 0028878052 scopus 로고
    • Gene therapy in a xenograft model of cystic fibrosis lung corrects chloride transport more effectively than the sodium defect
    • Goldman, M. J., Yang, Y., and Wilson, J. M. (1995) Gene therapy in a xenograft model of cystic fibrosis lung corrects chloride transport more effectively than the sodium defect. Nature Genet. 9, 126-131
    • (1995) Nature Genet. , vol.9 , pp. 126-131
    • Goldman, M.J.1    Yang, Y.2    Wilson, J.M.3
  • 16
    • 0028991829 scopus 로고
    • Persistence of replication-deficient adenovirus-mediated gene transfer in lungs of immune-deficient (nu/nu) mice
    • Zsengeller, Z. K., Wert, S. E., Hull, W. M., Hu, X., Yei, S., Trapnell, B. C., and Whitsett, J. A. (1995) Persistence of replication-deficient adenovirus-mediated gene transfer in lungs of immune-deficient (nu/nu) mice. Human Gene Ther. 6, 457-467
    • (1995) Human Gene Ther. , vol.6 , pp. 457-467
    • Zsengeller, Z.K.1    Wert, S.E.2    Hull, W.M.3    Hu, X.4    Yei, S.5    Trapnell, B.C.6    Whitsett, J.A.7
  • 17
    • 0028170353 scopus 로고
    • Correction of cAMP-stimulated fluid secretion in cystic fibrosis airway epithelia: Efficiency of adenovirus-mediated gene transfer in vitro
    • Zabner, J., Couture, L. A., Smith, A. E., and Welsh, M. J. (1994) Correction of cAMP-stimulated fluid secretion in cystic fibrosis airway epithelia: Efficiency of adenovirus-mediated gene transfer in vitro. Human Gene Ther. 5, 585-593
    • (1994) Human Gene Ther. , vol.5 , pp. 585-593
    • Zabner, J.1    Couture, L.A.2    Smith, A.E.3    Welsh, M.J.4
  • 18
    • 0026918861 scopus 로고
    • Efficiency of gene transfer for restoration of normal airway epithelial function in cystic fibrosis
    • Johnson, L. G., Olsen, J. C., Sarkadi, B., Moore, K. L., Swanstrom, R., and Boucher, R. C. (1992) Efficiency of gene transfer for restoration of normal airway epithelial function in cystic fibrosis. Nature Genet. 2, 21-25
    • (1992) Nature Genet. , vol.2 , pp. 21-25
    • Johnson, L.G.1    Olsen, J.C.2    Sarkadi, B.3    Moore, K.L.4    Swanstrom, R.5    Boucher, R.C.6
  • 19
    • 0029100239 scopus 로고
    • A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis
    • Knowles, M. R., Hohneker, K. W., Zhou, Z., Olsen, J. C., Noah, T. L., et al. (1995) A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis. N. Engl. J. Med. 333, 823-831
    • (1995) N. Engl. J. Med. , vol.333 , pp. 823-831
    • Knowles, M.R.1    Hohneker, K.W.2    Zhou, Z.3    Olsen, J.C.4    Noah, T.L.5
  • 20
    • 0029789790 scopus 로고    scopus 로고
    • Cardiovascular gene therapy: Current concepts
    • Fox, J. C. (1996) Cardiovascular gene therapy: Current concepts. Ther. Drug Monitoring 18, 410-122
    • (1996) Ther. Drug Monitoring , vol.18 , pp. 410-1122
    • Fox, J.C.1
  • 21
    • 0029860996 scopus 로고    scopus 로고
    • Reversal of potassium channel deficiency in cells from failing hearts by adenoviral gene transfer: A prototype for gene therapy for disorders of cardiac excitability and contractility
    • Nuss, H. B., Johns, D. C., Kaab, Tomaselli, G. F., Kass, D., Lawrence, J. H., and Marban, E. (1996) Reversal of potassium channel deficiency in cells from failing hearts by adenoviral gene transfer: a prototype for gene therapy for disorders of cardiac excitability and contractility. Gene Therapy 3, 900-912
    • (1996) Gene Therapy , vol.3 , pp. 900-912
    • Nuss, H.B.1    Johns, D.C.2    Kaab Tomaselli, G.F.3    Kass, D.4    Lawrence, J.H.5    Marban, E.6
  • 24
    • 0027163743 scopus 로고
    • Gene therapy of hemophilia B
    • Kurachi, K., and Yao, S.-N. (1993) Gene therapy of hemophilia B. Thromb. Haemostasis 70, 193-197
    • (1993) Thromb. Haemostasis , vol.70 , pp. 193-197
    • Kurachi, K.1    Yao, S.-N.2
  • 25
    • 0025874746 scopus 로고
    • Expression of human factor IX in rat capillary endothelial cells: Toward somatic gene therapy for hemophilia B
    • Yao, S.-N., Wilson, J. M., Nabel, E. G., Kurachi, S., Hachiya, H. L., and Kurachi, K. (1991) Expression of human factor IX in rat capillary endothelial cells: Toward somatic gene therapy for hemophilia B. Proc. Natl. Acad. Sci. USA 88, 8101-8105
    • (1991) Proc. Natl. Acad. Sci. USA , vol.88 , pp. 8101-8105
    • Yao, S.-N.1    Wilson, J.M.2    Nabel, E.G.3    Kurachi, S.4    Hachiya, H.L.5    Kurachi, K.6
  • 26
    • 0026486612 scopus 로고
    • Therapy via primary myoblasts: Long-term expression of factor IX protein following transplantation in vivo
    • Dai, Y., Roman, M., Naviaux, R. K., and Verma, I. M. Gene (1992) Therapy via primary myoblasts: Long-term expression of factor IX protein following transplantation in vivo. Proc. Natl. Acad. Sci. USA 89, 10892-10895
    • (1992) Proc. Natl. Acad. Sci. USA , vol.89 , pp. 10892-10895
    • Dai, Y.1    Roman, M.2    Naviaux, R.K.3    Verma, I.M.G.4
  • 29
    • 0026131053 scopus 로고
    • Persistent gene expression after retroviral gene transfer into liver cells in vivo
    • Kaleko, M., Garcia, J. V., and Miller, A. D. (1991) Persistent gene expression after retroviral gene transfer into liver cells in vivo. Human Gene Ther. 2, 27-32
    • (1991) Human Gene Ther. , vol.2 , pp. 27-32
    • Kaleko, M.1    Garcia, J.V.2    Miller, A.D.3
  • 30
    • 0027033259 scopus 로고
    • Hepatic gene therapy: Persistent expression of human 1-antitrypsin in mice after direct gene delivery in vivo
    • Kay, M. A., Li, Q., Liu, T.-J., Leland, F., Toman, C., Finegold, M., and Woo, S. L. C. (1992) Hepatic gene therapy: Persistent expression of human 1-antitrypsin in mice after direct gene delivery in vivo. Human Gene Ther. 3, 641-647
    • (1992) Human Gene Ther. , vol.3 , pp. 641-647
    • Kay, M.A.1    Li, Q.2    Liu, T.-J.3    Leland, F.4    Toman, C.5    Finegold, M.6    Woo, S.L.C.7
  • 33
    • 0027272371 scopus 로고
    • Efficient adenoviral-mediated ornithine transcarbamylase expression in deficient mouse and human hepatocytes
    • Morsy, M. A., Alford, E. L., Bett, A., Graham, F. L., and Caskey, C. T. (1993) Efficient adenoviral-mediated ornithine transcarbamylase expression in deficient mouse and human hepatocytes. J. Clin. Invest. 92, 1580-1586
    • (1993) J. Clin. Invest. , vol.92 , pp. 1580-1586
    • Morsy, M.A.1    Alford, E.L.2    Bett, A.3    Graham, F.L.4    Caskey, C.T.5
  • 34
    • 0027409026 scopus 로고
    • Adenovirus-mediated transfer of low density lipoprotein receptor gene acutely accelerates cholesterol clearance in normal mice
    • Herz, J., and Gerard, R. D. (1993) Adenovirus-mediated transfer of low density lipoprotein receptor gene acutely accelerates cholesterol clearance in normal mice. Proc. Natl. Acad. Sci. USA 90, 2812-2816
    • (1993) Proc. Natl. Acad. Sci. USA , vol.90 , pp. 2812-2816
    • Herz, J.1    Gerard, R.D.2
  • 35
    • 0027723616 scopus 로고
    • Adenovirus-mediated correction of the genetic defect in hepatocytes from patients with familial hypercholesterolemia
    • Kozarsky, K., Grossman, M., and Wilson, J. M. (1993) Adenovirus-mediated correction of the genetic defect in hepatocytes from patients with familial hypercholesterolemia. Somatic Cell Mol. Genet. 19, 449-458
    • (1993) Somatic Cell Mol. Genet. , vol.19 , pp. 449-458
    • Kozarsky, K.1    Grossman, M.2    Wilson, J.M.3
  • 36
    • 0027258140 scopus 로고
    • Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery
    • Ishibashi, S., Brown, M. S., Goldstein, J. L., Gerard, R. D., Hammer, R. E., and Herz, J. (1993) Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery. J. Clin. Invest. 92, 883-893
    • (1993) J. Clin. Invest. , vol.92 , pp. 883-893
    • Ishibashi, S.1    Brown, M.S.2    Goldstein, J.L.3    Gerard, R.D.4    Hammer, R.E.5    Herz, J.6
  • 37
    • 0028426914 scopus 로고
    • Liver-directed gene therapy: Prospects and problems
    • Strauss, M. (1994) Liver-directed gene therapy: Prospects and problems. Gene Therapy 1, 156-164
    • (1994) Gene Therapy , vol.1 , pp. 156-164
    • Strauss, M.1
  • 38
    • 0028234357 scopus 로고
    • In vivo correction of low density lipoprotein receptor deficiency in the Watanabe heritable hyperlipidemic rabbit with recombinant adenoviruses
    • Kozarsky, K. F., McKinley, D. R., Austin, L. L., Raper, S. E., Stratford-Perricaudet, L. D., and Wilson, J. M. (1994) In vivo correction of low density lipoprotein receptor deficiency in the Watanabe heritable hyperlipidemic rabbit with recombinant adenoviruses. J. Biol. Chem. 269, 13695-13702
    • (1994) J. Biol. Chem. , vol.269 , pp. 13695-13702
    • Kozarsky, K.F.1    McKinley, D.R.2    Austin, L.L.3    Raper, S.E.4    Stratford-Perricaudet, L.D.5    Wilson, J.M.6
  • 39
    • 0028899573 scopus 로고
    • Therapeutic serum concentrations of human alpha-1-antitrypsin after adenoviral-mediated gene transfer into mouse hepatocytes
    • Kay, M. A., Graham, F., Leland, F., and Woo, S. L. C. (1995) Therapeutic serum concentrations of human alpha-1-antitrypsin after adenoviral-mediated gene transfer into mouse hepatocytes. Hepatology 21, 815-819
    • (1995) Hepatology , vol.21 , pp. 815-819
    • Kay, M.A.1    Graham, F.2    Leland, F.3    Woo, S.L.C.4
  • 40
    • 0029988465 scopus 로고    scopus 로고
    • Effective treatment of familial hypercholesterolaemia in the mouse model using adenovirus-mediated transfer of the VLDL receptor gene
    • Kozarsky, K. F., Jooss, K., Donahee, M., Strauss, J. F., III, and Wilson, J. M. (1996) Effective treatment of familial hypercholesterolaemia in the mouse model using adenovirus-mediated transfer of the VLDL receptor gene. Nature Genet. 13, 54-62
    • (1996) Nature Genet. , vol.13 , pp. 54-62
    • Kozarsky, K.F.1    Jooss, K.2    Donahee, M.3    Strauss III, J.F.4    Wilson, J.M.5
  • 41
    • 0030042794 scopus 로고    scopus 로고
    • Prolonged metabolic correction in adult ornithine transcarbamylase-deficient mice with adenoviral vectors
    • Ye, X., Robinson, M. B., Batshaw, M. L., Furth, E. E., Smith, I., and Wilson, J. M. (1996) Prolonged metabolic correction in adult ornithine transcarbamylase-deficient mice with adenoviral vectors. J. Biol. Chem. 271, 3639-3646
    • (1996) J. Biol. Chem. , vol.271 , pp. 3639-3646
    • Ye, X.1    Robinson, M.B.2    Batshaw, M.L.3    Furth, E.E.4    Smith, I.5    Wilson, J.M.6
  • 44
    • 0029941649 scopus 로고    scopus 로고
    • Efficient adenovirus-mediated gene transfer to basal but not columnar cells of cartilaginous airway epithelia
    • Pickles, R. J., Barker, P. M., Ye, H., and Boucher, R. C. (1996) Efficient adenovirus-mediated gene transfer to basal but not columnar cells of cartilaginous airway epithelia. Human Gene Ther. 7, 921-931
    • (1996) Human Gene Ther. , vol.7 , pp. 921-931
    • Pickles, R.J.1    Barker, P.M.2    Ye, H.3    Boucher, R.C.4
  • 45
    • 0029820857 scopus 로고    scopus 로고
    • Adenovirus-mediated gene transfer to ciliated airway epithelia requires prolonged incubation time
    • Zabner, J., Zeiher, B. G., Friedman, E., and Welsh, M. J. (1996) Adenovirus-mediated gene transfer to ciliated airway epithelia requires prolonged incubation time. J. Virol. 70, 6994-7003
    • (1996) J. Virol. , vol.70 , pp. 6994-7003
    • Zabner, J.1    Zeiher, B.G.2    Friedman, E.3    Welsh, M.J.4
  • 46
    • 0028981979 scopus 로고
    • Expression of a v5 integrin is necessary for efficient adenovirus-mediated gene transfer in the human airway
    • Goldman, J. J., and Wilson, J. M. (1995) Expression of a v5 integrin is necessary for efficient adenovirus-mediated gene transfer in the human airway. J. Virol. 69, 5951-5958
    • (1995) J. Virol. , vol.69 , pp. 5951-5958
    • Goldman, J.J.1    Wilson, J.M.2
  • 47
    • 0029794845 scopus 로고    scopus 로고
    • Gradient of RGD-dependent entry of adenoviral vector in nasal and intrapulmonary epithelia: Implications for gene therapy of cystic fibrosis
    • Goldman, M., Su, Q., and Wilson, J. M. (1996) Gradient of RGD-dependent entry of adenoviral vector in nasal and intrapulmonary epithelia: Implications for gene therapy of cystic fibrosis. Gene Ther. 3, 811-818
    • (1996) Gene Ther. , vol.3 , pp. 811-818
    • Goldman, M.1    Su, Q.2    Wilson, J.M.3
  • 48
    • 0029794681 scopus 로고    scopus 로고
    • Targeted adenovirus gene transfer to endothelial and smooth muscle cells by using bispecific antibodies
    • Wickham, T. J., Segal, D. M., Roelvink, P. W., Carrion, M. E., Lizonova, A., Lee, G. M., and Kovesdi, I. (1996) Targeted adenovirus gene transfer to endothelial and smooth muscle cells by using bispecific antibodies. J. Virol. 70, 6831-6838
    • (1996) J. Virol. , vol.70 , pp. 6831-6838
    • Wickham, T.J.1    Segal, D.M.2    Roelvink, P.W.3    Carrion, M.E.4    Lizonova, A.5    Lee, G.M.6    Kovesdi, I.7
  • 49
    • 0028464351 scopus 로고
    • Strategies to achieve targeted gene delivery via the receptor-mediated endocytosis pathway
    • Michael S. I., and Curiel, D. T. (1995) Strategies to achieve targeted gene delivery via the receptor-mediated endocytosis pathway. Gene Ther. 1, 223-232
    • (1995) Gene Ther. , vol.1 , pp. 223-232
    • Michael, S.I.1    Curiel, D.T.2
  • 51
    • 0029793812 scopus 로고    scopus 로고
    • Generation of recombinant adenovirus vectors with modified fibers for altering viral tropism
    • Krasnykh, V. N., Mikheeva, G. V., Douglas, J. T., and Curiel, D. T. (1996) Generation of recombinant adenovirus vectors with modified fibers for altering viral tropism. J. Virol. 70, 6839-6846
    • (1996) J. Virol. , vol.70 , pp. 6839-6846
    • Krasnykh, V.N.1    Mikheeva, G.V.2    Douglas, J.T.3    Curiel, D.T.4
  • 53
    • 0028946357 scopus 로고
    • Targeted vectors for gene therapy
    • Miller, N., and Vile, R. (1995) Targeted vectors for gene therapy. FASEB J. 9, 190-199
    • (1995) FASEB J. , vol.9 , pp. 190-199
    • Miller, N.1    Vile, R.2
  • 56
    • 0028484704 scopus 로고
    • MHC class I-restricted cytotoxic T lymphocytes to viral antigens destroy hepatocytes in mice infected with E1-deleted recombinant adenoviruses
    • Yang, Y., Ertl, H. C., and Wilson, J. M. (1995) MHC class I-restricted cytotoxic T lymphocytes to viral antigens destroy hepatocytes in mice infected with E1-deleted recombinant adenoviruses. Immunity 1, 433-442
    • (1995) Immunity , vol.1 , pp. 433-442
    • Yang, Y.1    Ertl, H.C.2    Wilson, J.M.3
  • 57
    • 0028937785 scopus 로고
    • Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses
    • Yang, Y., Li, Q., Ertl, H. C., and Wilson, J. M. (1995) Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses. J. Virol. 69, 2004-2015
    • (1995) J. Virol. , vol.69 , pp. 2004-2015
    • Yang, Y.1    Li, Q.2    Ertl, H.C.3    Wilson, J.M.4
  • 58
    • 0029093070 scopus 로고
    • Upregulation of class I major histocompatibility complex antigens by Interferon gamma is necessary for T-cell-mediated elimination of recombinant adenovirus-infected hepatocytes in vivo
    • Yang, Y., Xiang, Z., Ertl, H. C., and Wilson, J. M. (1995) Upregulation of class I major histocompatibility complex antigens by Interferon gamma is necessary for T-cell-mediated elimination of recombinant adenovirus-infected hepatocytes in vivo. Proc. Natl. Acad. Sci. USA 92, 7257-7261
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 7257-7261
    • Yang, Y.1    Xiang, Z.2    Ertl, H.C.3    Wilson, J.M.4
  • 59
    • 0028246338 scopus 로고
    • Ablation of E2A in rebcombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver
    • Engelhardt, J. F., Ye, X., Doranz, B., and Wilson, J. M. (1994) Ablation of E2A in rebcombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver. Proc. Natl. Acad. Sci. USA 91, 6196-6200
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , pp. 6196-6200
    • Engelhardt, J.F.1    Ye, X.2    Doranz, B.3    Wilson, J.M.4
  • 60
    • 0029966514 scopus 로고    scopus 로고
    • Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis
    • Fisher, K. J., Choi, H., Burda, J., Chen, S. J., and Wilson, J. M. (1996) Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis. Virology 217, 11-22
    • (1996) Virology , vol.217 , pp. 11-22
    • Fisher, K.J.1    Choi, H.2    Burda, J.3    Chen, S.J.4    Wilson, J.M.5
  • 61
    • 0029664338 scopus 로고    scopus 로고
    • Elimination of both E1 and E2 from adenovirus vectors further improves prospects for in vivo human gene therapy
    • Gorziglia, M. I., Kadan, M. J., Yei, S., Lim, J., Lee, G. M., Luthra, R., and Trapnell, B. C. (1996) Elimination of both E1 and E2 from adenovirus vectors further improves prospects for in vivo human gene therapy. J. Virol. 70, 4173-4178
    • (1996) J. Virol. , vol.70 , pp. 4173-4178
    • Gorziglia, M.I.1    Kadan, M.J.2    Yei, S.3    Lim, J.4    Lee, G.M.5    Luthra, R.6    Trapnell, B.C.7
  • 62
    • 0027462711 scopus 로고
    • Monitoring foreign gene expression by a human adenovirus-based vector using the firefly luciferase gene as a reporter
    • Mittal, S. K., McDermott, M. R., Johnson, D. C., Prevec, L., and Graham, F. L. (1993) Monitoring foreign gene expression by a human adenovirus-based vector using the firefly luciferase gene as a reporter. Virus Res. 28, 67-90
    • (1993) Virus Res. , vol.28 , pp. 67-90
    • Mittal, S.K.1    McDermott, M.R.2    Johnson, D.C.3    Prevec, L.4    Graham, F.L.5
  • 64
    • 77957042700 scopus 로고
    • Techniques for human adenovirus vector construction and characterization
    • Hitt, M., Bett, A. J., Addison, G. L., Prevec, L., and Graham, F. L. (1995) Techniques for human adenovirus vector construction and characterization. Methods Mol. Genet. 7, 13-30
    • (1995) Methods Mol. Genet. , vol.7 , pp. 13-30
    • Hitt, M.1    Bett, A.J.2    Addison, G.L.3    Prevec, L.4    Graham, F.L.5
  • 65
    • 0028871549 scopus 로고
    • Adenovirus vectors as recombinant viral vaccines
    • Imler, J.-L. (1995) Adenovirus vectors as recombinant viral vaccines. Vaccine 13, 1143-1151
    • (1995) Vaccine , vol.13 , pp. 1143-1151
    • Imler, J.-L.1
  • 66
    • 0028926021 scopus 로고
    • Retroviruses as vectors
    • Vile, R. G., and Russell, S. J. (1995) Retroviruses as vectors. Br. Med. Bull. 51, 12-30
    • (1995) Br. Med. Bull. , vol.51 , pp. 12-30
    • Vile, R.G.1    Russell, S.J.2
  • 70
    • 0025064567 scopus 로고
    • Hepatic gene transfer in animals using retroviruses containing the promoter from the gene for phosphoenolpyruvate carboxykinase
    • Hatzoglou, M., Lamers, W., Bosch, F., Wynshaw-Boris, A., Clapp, D. W., and Hanson, R. W. (1990) Hepatic gene transfer in animals using retroviruses containing the promoter from the gene for phosphoenolpyruvate carboxykinase. J. Biol. Chem. 265, 17285-17293
    • (1990) J. Biol. Chem. , vol.265 , pp. 17285-17293
    • Hatzoglou, M.1    Lamers, W.2    Bosch, F.3    Wynshaw-Boris, A.4    Clapp, D.W.5    Hanson, R.W.6
  • 72
    • 0027748178 scopus 로고
    • Hepatic gene therapy: Efficient retroviral-mediated gene transfer into rat hepatocytes in vivo
    • Kolodka, T. M., Finegold, M., and Woo, S. L. C. (1993) Hepatic gene therapy: Efficient retroviral-mediated gene transfer into rat hepatocytes in vivo. Somatic Cell Mol. Genet. 19, 491-497
    • (1993) Somatic Cell Mol. Genet. , vol.19 , pp. 491-497
    • Kolodka, T.M.1    Finegold, M.2    Woo, S.L.C.3
  • 73
    • 0027174251 scopus 로고
    • Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo
    • Dunckley, M. G., Wells, D. J., Walsh, F. S., and Dickson, G. (1993) Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo. Human Mol. Genet. 2, 717-723
    • (1993) Human Mol. Genet. , vol.2 , pp. 717-723
    • Dunckley, M.G.1    Wells, D.J.2    Walsh, F.S.3    Dickson, G.4
  • 74
    • 0027418929 scopus 로고
    • In vivo regional delivery of retrovirally mediated foreign genes to rat liver cells: Need for partial hepatectomy for successful foreign gene expression
    • Moscioni, A. D., Rozga, J., Neuzil, D.F., Overell, R. W., Holt, J. T., and Demetriou, A. A. (1993) In vivo regional delivery of retrovirally mediated foreign genes to rat liver cells: Need for partial hepatectomy for successful foreign gene expression. Surgery 113, 304-311
    • (1993) Surgery , vol.113 , pp. 304-311
    • Moscioni, A.D.1    Rozga, J.2    Neuzil, D.F.3    Overell, R.W.4    Holt, J.T.5    Demetriou, A.A.6
  • 75
    • 0027748178 scopus 로고
    • Hepatic gene therapy: Efficient retroviral-mediated gene transfer into rat hepatocytes in vivo
    • Kolodka, T. M., Finegold, M., and Woo, S. L. C. (1993) Hepatic gene therapy: Efficient retroviral-mediated gene transfer into rat hepatocytes in vivo. Somatic Cell Mol. Genet. 19, 491-497
    • (1993) Somatic Cell Mol. Genet. , vol.19 , pp. 491-497
    • Kolodka, T.M.1    Finegold, M.2    Woo, S.L.C.3
  • 78
    • 0028071740 scopus 로고
    • Recombinant retroviral vector delivered intramuscularly localizes to the site of injection in mice
    • Sajjadi, N., Kamantigue, E., Edwards, W., Howard, T., Jolly, D., Mento, S., and Chada, S. (1994) Recombinant retroviral vector delivered intramuscularly localizes to the site of injection in mice. Human Gene Ther. 5, 693-699
    • (1994) Human Gene Ther. , vol.5 , pp. 693-699
    • Sajjadi, N.1    Kamantigue, E.2    Edwards, W.3    Howard, T.4    Jolly, D.5    Mento, S.6    Chada, S.7
  • 79
    • 0029147629 scopus 로고
    • Efficiency of in vivo gene transfer using murine retroviral vectors is strain-dependent in mice
    • Fassati, A., Wells, D. J., Walsh, F. S., and Dickson, G. (1995) Efficiency of in vivo gene transfer using murine retroviral vectors is strain-dependent in mice. Human Gene Ther. 6, 1177-1183
    • (1995) Human Gene Ther. , vol.6 , pp. 1177-1183
    • Fassati, A.1    Wells, D.J.2    Walsh, F.S.3    Dickson, G.4
  • 80
    • 0028963345 scopus 로고
    • Gene therapy for diabetes mellitus in rats by hepatic expression of insulin
    • Kolodka, T. M., Finegold, M., Moss, L., and Woo, S. L. C. (1995) Gene therapy for diabetes mellitus in rats by hepatic expression of insulin. Proc. Natl. Acad. Sci. USA 92, 3293-3297
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 3293-3297
    • Kolodka, T.M.1    Finegold, M.2    Moss, L.3    Woo, S.L.C.4
  • 81
    • 0029849764 scopus 로고    scopus 로고
    • A simple and efficient method for the concentration and purification of recombinant retrovirus for increased hepatocyte transduction in vivo
    • Bowles, N. E., Eisensmith, R. C., Mohuiddin, R., Pyron, M., and Woo, S. L. C. (1996) A simple and efficient method for the concentration and purification of recombinant retrovirus for increased hepatocyte transduction in vivo. Human Gene Ther. 7, 1735-1742
    • (1996) Human Gene Ther. , vol.7 , pp. 1735-1742
    • Bowles, N.E.1    Eisensmith, R.C.2    Mohuiddin, R.3    Pyron, M.4    Woo, S.L.C.5
  • 82
    • 0029893033 scopus 로고    scopus 로고
    • Development of amphotropic murine retrovirus vectors resistant to inactivation by human serum
    • Pensiero, M. N., Wysocki, C. A., Nader, K., and Kikuchi, G. E. (1996) Development of amphotropic murine retrovirus vectors resistant to inactivation by human serum. Human Gene Ther. 7, 1095-1101
    • (1996) Human Gene Ther. , vol.7 , pp. 1095-1101
    • Pensiero, M.N.1    Wysocki, C.A.2    Nader, K.3    Kikuchi, G.E.4
  • 83
    • 0018268096 scopus 로고
    • Complement-mediated lysis of type-C virus: Effect of primate and human sera on various retroviruses
    • Sherwin, S. A., Benveniste, R. E., and Todaro, G. J. (1978) Complement-mediated lysis of type-C virus: Effect of primate and human sera on various retroviruses. Int. J. Cancer 21, 6-11
    • (1978) Int. J. Cancer , vol.21 , pp. 6-11
    • Sherwin, S.A.1    Benveniste, R.E.2    Todaro, G.J.3
  • 85
    • 0028138555 scopus 로고
    • Type C retrovirus inactivation by human complement is determined by both the viral genome and the producer cell
    • Takeuchi, Y., Cosset, F.-L.C., Lachmann, P. J., Okada, H., Weiss, R. A., Collins, and M. K. L. (1994) Type C retrovirus inactivation by human complement is determined by both the viral genome and the producer cell. J. Virol. 68, 8001-8007
    • (1994) J. Virol. , vol.68 , pp. 8001-8007
    • Takeuchi, Y.1    Cosset, F.-L.C.2    Lachmann, P.J.3    Okada, H.4    Weiss, R.A.5    Collins, M.K.L.6
  • 86
    • 0028991828 scopus 로고
    • Protection of retroviral vector particles in human blood through complement inhibition
    • Rother, R. P., Squinto, S. P., Mason, J. M., and Rollins, S. A. (1995) Protection of retroviral vector particles in human blood through complement inhibition. Human Gene Ther. 6, 429-435
    • (1995) Human Gene Ther. , vol.6 , pp. 429-435
    • Rother, R.P.1    Squinto, S.P.2    Mason, J.M.3    Rollins, S.A.4
  • 88
    • 0029154407 scopus 로고
    • The effects of human serum and cerebrospinal fluid on retroviral vectors and packaging cell lines
    • Russell, D. W., Berger, M. S., and Miller, A. D. (1995) The effects of human serum and cerebrospinal fluid on retroviral vectors and packaging cell lines. Human Gene Ther. 6, 635-641
    • (1995) Human Gene Ther. , vol.6 , pp. 635-641
    • Russell, D.W.1    Berger, M.S.2    Miller, A.D.3
  • 89
    • 0025610750 scopus 로고
    • Gene delivery to glioma cells in rat brain by grafting of a retrovirus packaging cell line
    • Short, M. P., Choi, B. C., Lee, J. K., Malick, A., Breakefield, X. O., and Martuza, R. L. (1990) Gene delivery to glioma cells in rat brain by grafting of a retrovirus packaging cell line. J. Neurosci. Res. 27, 427-433
    • (1990) J. Neurosci. Res. , vol.27 , pp. 427-433
    • Short, M.P.1    Choi, B.C.2    Lee, J.K.3    Malick, A.4    Breakefield, X.O.5    Martuza, R.L.6
  • 90
    • 0026772206 scopus 로고
    • In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors
    • Culver, K. W., Ram, Z., Wallbridge, S., Ishii, H., Oldfield, E. H., and Blaese, R. M. (1992) In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors. Science 256, 1550-1552
    • (1992) Science , vol.256 , pp. 1550-1552
    • Culver, K.W.1    Ram, Z.2    Wallbridge, S.3    Ishii, H.4    Oldfield, E.H.5    Blaese, R.M.6
  • 92
    • 0027531548 scopus 로고
    • In situ retroviral-mediated gene transfer for the treatment of brain tumors in rats
    • Ram, Z., Culver, K. W., Walbridge, S., Blaese, R. M., and Oldfield, E. H. (1993) In situ retroviral-mediated gene transfer for the treatment of brain tumors in rats. Cancer Res. 53, 83-88
    • (1993) Cancer Res. , vol.53 , pp. 83-88
    • Ram, Z.1    Culver, K.W.2    Walbridge, S.3    Blaese, R.M.4    Oldfield, E.H.5
  • 93
    • 0027317796 scopus 로고
    • Toxicity studies of retroviral-mediated gene transfer for the treatment of brain tumors
    • Ram, Z., Culver, K. W., Walbridge, S., Frank, J. A., Blaese, R. M., and Oldfield, E. H. (1993) Toxicity studies of retroviral-mediated gene transfer for the treatment of brain tumors. J. Neurosurg. 79, 400-407
    • (1993) J. Neurosurg. , vol.79 , pp. 400-407
    • Ram, Z.1    Culver, K.W.2    Walbridge, S.3    Frank, J.A.4    Blaese, R.M.5    Oldfield, E.H.6
  • 96
    • 0029548580 scopus 로고
    • Retroviral-mediated in vivo gene transfer into muscle cells and synthesis of human factor IX in mice
    • Baru, M., Sha'anani, J., and Nur, I. (1995) Retroviral-mediated in vivo gene transfer into muscle cells and synthesis of human factor IX in mice. Intervirology 38, 356-360
    • (1995) Intervirology , vol.38 , pp. 356-360
    • Baru, M.1    Sha'anani, J.2    Nur, I.3
  • 97
    • 0029918899 scopus 로고    scopus 로고
    • Transplantation of retroviral producer cells for in vivo gene transfer into mouse skeletal muscle
    • Fassati, A., Wells, D. J., Walsh, F. S., and Dickson, G. (1996) Transplantation of retroviral producer cells for in vivo gene transfer into mouse skeletal muscle. Human Gene Ther. 7, 595-602
    • (1996) Human Gene Ther. , vol.7 , pp. 595-602
    • Fassati, A.1    Wells, D.J.2    Walsh, F.S.3    Dickson, G.4
  • 98
    • 0029146695 scopus 로고
    • Gene therapy of metastatic cancer by in vivo retroviral gene targeting
    • Hurford, R. K., Jr., Dranoff, G., Mulligan, R. C., and Tepper, R. I. (1995) Gene therapy of metastatic cancer by in vivo retroviral gene targeting. Nature Genet. 10, 430-435
    • (1995) Nature Genet. , vol.10 , pp. 430-435
    • Hurford Jr., R.K.1    Dranoff, G.2    Mulligan, R.C.3    Tepper, R.I.4
  • 99
    • 0029997197 scopus 로고    scopus 로고
    • Retroviral vector producer cell killing in human serum is mediated by natural antibody and complement: Strategies for evading the humoral immune response
    • Rollins, S. A., Birks, C. W., Setter, E., Squinto, S. P., and, Rother, R. P. (1996) Retroviral vector producer cell killing in human serum is mediated by natural antibody and complement: Strategies for evading the humoral immune response. Human Gene Ther. 7, 619-626
    • (1996) Human Gene Ther. , vol.7 , pp. 619-626
    • Rollins, S.A.1    Birks, C.W.2    Setter, E.3    Squinto, S.P.4    Rother, R.P.5
  • 100
    • 0027236954 scopus 로고
    • Production of high-titer helper-free retroviruses by transient transfection
    • Pear, W. S., Nolan, G. P., Scott, M. L., and Baltimore, D. (1993) Production of high-titer helper-free retroviruses by transient transfection. Proc. Natl. Acad. Sci. USA 90, 8392-8396
    • (1993) Proc. Natl. Acad. Sci. USA , vol.90 , pp. 8392-8396
    • Pear, W.S.1    Nolan, G.P.2    Scott, M.L.3    Baltimore, D.4
  • 101
    • 0028577834 scopus 로고
    • Virofection: A new procedure to achieve stable expression of genes transferred into early embryos
    • Flamant, F., Demeneix, B., Benoist, G., Markossian-Belin, S., and Samarut, J. (1994) Virofection: A new procedure to achieve stable expression of genes transferred into early embryos. Int J. Dev. Biol, 38, 751-757
    • (1994) Int J. Dev. Biol , vol.38 , pp. 751-757
    • Flamant, F.1    Demeneix, B.2    Benoist, G.3    Markossian-Belin, S.4    Samarut, J.5
  • 102
    • 0029149328 scopus 로고
    • Enhanced transduction efficiency of retroviral vectors coprecipitated with calcium phosphate
    • Morling, F. J., and Russell, S. J. (1995) Enhanced transduction efficiency of retroviral vectors coprecipitated with calcium phosphate. Gene Therapy 2, 504-508
    • (1995) Gene Therapy , vol.2 , pp. 504-508
    • Morling, F.J.1    Russell, S.J.2
  • 103
    • 0029132243 scopus 로고
    • Virofection: A one-step procedure for using replication-defective retrovirus vectors
    • Flamant, F., and Samarut, J. (1995) Virofection: A one-step procedure for using replication-defective retrovirus vectors. Virology 211, 234-240
    • (1995) Virology , vol.211 , pp. 234-240
    • Flamant, F.1    Samarut, J.2
  • 104
    • 0028097848 scopus 로고
    • kat: A high efficiency retroviral transduction system for primary human T lymphocytes
    • Finer, M. H., Dull, T. J., Qin, L., Farson, D., and Roberts, M. R. (1994) kat: A high efficiency retroviral transduction system for primary human T lymphocytes. Blood 83, 43-50
    • (1994) Blood , vol.83 , pp. 43-50
    • Finer, M.H.1    Dull, T.J.2    Qin, L.3    Farson, D.4    Roberts, M.R.5
  • 105
    • 0028860281 scopus 로고
    • Generation of high-titer retroviral vectors following receptor-mediated, adenovirus-augmented transfection
    • von Rüden, T., Stingl, L., Cotten, M., Wagner, C., and Zatloukal, K. (1995) Generation of high-titer retroviral vectors following receptor-mediated, adenovirus-augmented transfection. BioTechniques 18, 484-488
    • (1995) BioTechniques , vol.18 , pp. 484-488
    • Von Rüden, T.1    Stingl, L.2    Cotten, M.3    Wagner, C.4    Zatloukal, K.5
  • 107
    • 0025279872 scopus 로고
    • Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection
    • Miller, D. G., Adam, M. A., and Miller, A. D. (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
    • (1990) Mol. Cell. Biol. , vol.10 , pp. 4239-4242
    • Miller, D.G.1    Adam, M.A.2    Miller, A.D.3
  • 108
    • 0029088057 scopus 로고
    • A modified urokinase plasminogen activator induces liver regeneration without bleeding
    • Lieber, A., Peeters, M. J., Gown, A., Perkins, J., and Kay, M. A. (1995) A modified urokinase plasminogen activator induces liver regeneration without bleeding. Human Gene Ther. 6, 1029-1037
    • (1995) Human Gene Ther. , vol.6 , pp. 1029-1037
    • Lieber, A.1    Peeters, M.J.2    Gown, A.3    Perkins, J.4    Kay, M.A.5
  • 109
    • 0030452791 scopus 로고
    • Proliferation induced by keratinosyte growth factor enhances in vivo retroviral-mediated gene transfer to mouse hepatocytes
    • Bosch, A., McCray, P. B., Jr., Chang, S. M., Ulich, T. R., Simonet, W. S., Jolly, D. J., and Davidson, B. L. (1966) Proliferation induced by keratinosyte growth factor enhances in vivo retroviral-mediated gene transfer to mouse hepatocytes. J. Clin. Invest. 98, 2683-2687
    • (1966) J. Clin. Invest. , vol.98 , pp. 2683-2687
    • Bosch, A.1    McCray, P.B.2    Jr3    Chang, S.M.4    Ulich, T.R.5    Simonet, W.S.6    Jolly, D.J.7    Davidson, B.L.8
  • 110
    • 0028324325 scopus 로고
    • High-efficiency gene transfer employing adenovirus-polysine-DNA complexes
    • Curiel, D. T. (1994) High-efficiency gene transfer employing adenovirus-polysine-DNA complexes. Nat. Immunity 13, 141-164
    • (1994) Nat. Immunity , vol.13 , pp. 141-164
    • Curiel, D.T.1
  • 111
    • 0029823797 scopus 로고    scopus 로고
    • A novel adenovirus-adeno-associated virus hybrid vector that displays efficient rescue and delivers of the AAV genome
    • Fisher, K. J., Kelley, W. M., Burda, J. F., and Wilson, J. M. (1996) A novel adenovirus-adeno-associated virus hybrid vector that displays efficient rescue and delivers of the AAV genome. Human Gene Ther. 7, 2079-2087
    • (1996) Human Gene Ther. , vol.7 , pp. 2079-2087
    • Fisher, K.J.1    Kelley, W.M.2    Burda, J.F.3    Wilson, J.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.