메뉴 건너뛰기




Volumn 15, Issue 9, 1997, Pages 866-870

Stable in vivo gene transduction via a novel adenoviral/retroviral chimeric vector

Author keywords

Chimeric viral vectors; Gene therapy

Indexed keywords

ADENOVIRUS; ANIMAL CELL; ARTICLE; CELL STRAIN 3T3; EXPRESSION VECTOR; GENE EXPRESSION; GENE TARGETING; GENE THERAPY; GENE TRANSFER; GENETIC TRANSDUCTION; NONHUMAN; PRIORITY JOURNAL; RETROVIRUS;

EID: 0030775646     PISSN: 10870156     EISSN: 15461696     Source Type: Journal    
DOI: 10.1038/nbt0997-866     Document Type: Article
Times cited : (133)

References (47)
  • 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
  • 3
    • 0026430686 scopus 로고
    • Gene therapeutics
    • Felgner, P.L. and Rhodes, G. 1991. Gene therapeutics. Nature 349:351-352.
    • (1991) Nature , vol.349 , pp. 351-352
    • Felgner, P.L.1    Rhodes, G.2
  • 4
    • 0026775132 scopus 로고
    • Concepts and strategies for human gene therapy
    • Roemer, K. and Friedmann, T. 1992. Concepts and strategies for human gene therapy. Eur. J. Biochem. 208:211-225.
    • (1992) Eur. J. Biochem , vol.208 , pp. 211-225
    • Roemer, K.1    Friedmann, T.2
  • 6
    • 0027980227 scopus 로고
    • Cellular gene therapy: An overview
    • Klein, H.G. 1994. Cellular gene therapy: An overview. J. Clin. Apheres. 9:139-141.
    • (1994) J. Clin. Apheres , vol.9 , pp. 139-141
    • Klein, H.G.1
  • 7
    • 0026486612 scopus 로고
    • Gene therapy via primary myoblasts: Long-term expression of fact IX protein following transplantation in vivo
    • Dai, Y., Roman, M., Naviaux, R.K., and Verman, I.M. 1992. Gene therapy via primary myoblasts: Long-term expression of fact 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    Verman, I.M.4
  • 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
  • 10
    • 0029789790 scopus 로고    scopus 로고
    • Cardiovascular gene therapy: Current concepts
    • Fox, J.C. 1996. Cardiovascular gene therapy: Current concepts. Therapeutic Drug Monitoring 18:410-422.
    • (1996) Therapeutic Drug Monitoring , vol.18 , pp. 410-422
    • Fox, J.C.1
  • 11
    • 0028009619 scopus 로고
    • Gene therapy and the hemophilias
    • Lozier, J.N. and Brinkjous, K.M. 1994. Gene therapy and the hemophilias. JAMA 271:47-51.
    • (1994) JAMA , vol.271 , pp. 47-51
    • Lozier, J.N.1    Brinkjous, K.M.2
  • 13
  • 14
    • 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., 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
  • 15
    • 0027409026 scopus 로고
    • Adenovirus-mediated transfer of low density lipoprotein receptor gene acutely accelerates cholersterol clearance in normal mice
    • Herz, J. and Gerard, R.D. 1993. Adenovirus-mediated transfer of low density lipoprotein receptor gene acutely accelerates cholersterol 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
  • 16
    • 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 Molec. Gen. 19:449-458.
    • (1993) Somatic Cell Molec. Gen , vol.19 , pp. 449-458
    • Kozarsky, K.1    Grossman, M.2    Wilson, J.M.3
  • 17
    • 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
  • 18
    • 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 Genetics 13:54-62.
    • (1996) Nature Genetics , vol.13 , pp. 54-62
    • Kozarsky, K.F.1    Jooss, K.2    Donahee, M.3    Strauss, J.4    Wilson, J.M.5
  • 19
    • 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
  • 21
    • 0029028989 scopus 로고
    • Clearance of adenovirus-infected hepatocytes by MHC class I-restricted CD4+ CTLs in vivo
    • Yang, Y. and Wilson, J.M. 1995. Clearance of adenovirus-infected hepatocytes by MHC class I-restricted CD4+ CTLs in vivo. J. Immunol. 155:2564-2570.
    • (1995) J. Immunol , vol.155 , pp. 2564-2570
    • Yang, Y.1    Wilson, J.M.2
  • 22
    • 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., Ertle, 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    Ertle, H.C.2    Wilson, J.M.3
  • 23
    • 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
  • 25
    • 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 Molec. Gen. 19:491-497.
    • (1993) Somatic Cell Molec. Gen , vol.19 , pp. 491-497
    • Kolodka, T.M.1    Finegold, M.2    Woo, S.L.C.3
  • 26
    • 0027174251 scopus 로고
    • Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo
    • Dunckley, M.G., Wells, D.J., Welsh, F.S., and Dickson, G. 1993. Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo. Human Molecular Genetics 2:717-723.
    • (1993) Human Molecular Genetics , vol.2 , pp. 717-723
    • Dunckley, M.G.1    Wells, D.J.2    Welsh, F.S.3    Dickson, G.4
  • 27
    • 0027418929 scopus 로고
    • In vivo regional delivery of retrovirally mediated foreign genes to rat liver cells: Need for partial hepatectomy for succcessful 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 succcessful 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
  • 28
    • 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 Molec. Gen. 19:491-497.
    • (1993) Somatic Cell Molec. Gen , vol.19 , pp. 491-497
    • Kolodka, T.M.1    Finegold, M.2    Woo, S.L.C.3
  • 30
    • 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
  • 31
    • 0026772206 scopus 로고    scopus 로고
    • In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors
    • Culver, K.W., Ram, Z., Walbridge, S., Ishii, H., Oldfield, E.H., and Blaese, R.M. In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors. Science 256:1550-1552.
    • Science , vol.256 , pp. 1550-1552
    • Culver, K.W.1    Ram, Z.2    Walbridge, S.3    Ishii, H.4    Oldfield, E.H.5    Blaese, R.M.6
  • 33
    • 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 Odfield, 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    Odfield, E.H.5
  • 34
    • 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
  • 37
    • 0029997197 scopus 로고    scopus 로고
    • Retroviral vector producer cell killing in human serum in 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 in mediated by natural antibody and complement: Strategies for evading the humoral immune response. Human Gene Therapy 7:619-626.
    • (1996) Human Gene Therapy , vol.7 , pp. 619-626
    • Rollins, S.A.1    Birks, C.W.2    Setter, E.3    Squinto, S.P.4    Rother, R.P.5
  • 38
    • 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
  • 39
    • 0028577834 scopus 로고
    • Virofection: A new procedure to achieve stable expression of genes transferred into early embryos
    • Flamant, F., Demeneix, B., Benoist, C., 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, C.3    Markossian-Belin, S.4    Samarut, J.5
  • 40
    • 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
  • 41
    • 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
  • 42
    • 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
  • 44
    • 0028559768 scopus 로고
    • An efficient and flexible system for-construction of adenovirus vectors with insertions or deletions in early regions 1 and 3
    • Bett AJ., Haddara W., Prevec L., Graham FL. An efficient and flexible system for-construction of adenovirus vectors with insertions or deletions in early regions 1 and 3. Proc Natl Acad Sci USA 91:8802-6 (1994).
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 8802-8806
    • Bett, A.J.1    Haddara, W.2    Prevec, L.3    Graham, F.L.4
  • 45
    • 0028324325 scopus 로고
    • High-efficiency gene transfer employing adenovirus-polylysine-DNA complexes
    • Curiel, D.T. 1994. High-efficiency gene transfer employing adenovirus-polylysine-DNA complexes. Natural Immunity 13:141-164.
    • (1994) Natural Immunity , vol.13 , pp. 141-164
    • Curiel, D.T.1
  • 46
    • 0029823797 scopus 로고    scopus 로고
    • A novel adenovirus-adeno-associated virus hybrid vector that displays efficient rescue and delivery 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 delivery of the AAV genome. Human Gene Therapy 7:2079-2087.
    • (1996) Human Gene Therapy , vol.7 , pp. 2079-2087
    • Fisher, K.J.1    Kelley, W.M.2    Burda, J.F.3    Wilson, J.M.4
  • 47
    • 0021894711 scopus 로고
    • Isolation from cats of an endogenous type C virus with a novel envelope
    • Haapala, D.K., Robey, W.G., Oroszlan, S.D., and Tsai, W.P. 1985. Isolation from cats of an endogenous type C virus with a novel envelope. J. Virology 53:827-833.
    • (1985) J. Virology , vol.53 , pp. 827-833
    • Haapala, D.K.1    Robey, W.G.2    Oroszlan, S.D.3    Tsai, W.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.