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      KCI등재 SCI SCIE SCOPUS

      Delivery of Factor VIII Gene into Skeletal Muscle Cells Using Lentiviral Vector

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      https://www.riss.kr/link?id=A101618453

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      다국어 초록 (Multilingual Abstract)

      Purpose: This study was designed to investigate whether transduction of lentiviral vectors (LV) carrying human coagulation factor VIII (hFVIII) cDNA into skeletal muscle could increase circulating hFVIII concentrations. Materials and Methods: A LV con...

      Purpose: This study was designed to investigate whether transduction of lentiviral vectors (LV) carrying human coagulation factor VIII (hFVIII) cDNA into skeletal muscle could increase circulating hFVIII concentrations.
      Materials and Methods: A LV containing bacterial LacZ gene as a control or human FVIII gene was intramuscularly administered into the thigh muscle of 5 weeks old Sparague-Dawley rats. The plasma human FVIII concentration and neutralizing anti-FVIII antibodies were measured for up to 12 weeks in these experimental animals. Results: The plasma human FVIII levels in the rats injected with LV carrying FVIII cDNA peaked at post-injection 1st week (5.19 ± 0.14 ng/mL vs. 0.21 ± 0.05 ng/mL in control rats , p < 0.05). Elevated hFVIII concentrations were maintained for 4 weeks (2.52 ± 0.83 ng/mL vs. 0.17 ± 0.08 ng/mL in control rats, p < 0.05)after a single intramuscular injection. In the Bethesda assay, neutralizing antibodies for FVIII protein were detected only in FVIII-LV injected rats by the 10th week, but not in control rats. Conclusion: This study suggested that a single administration of an advanced generation LV carrying the human FVIII cDNA resulted in elevation of FVIII level in immune competent rats, and that this gene transfer approach to the skeletal muscle could be an effective tool in treatment of hemophilia A.

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      참고문헌 (Reference)

      1 VandenDriessche T, "Viral vector-mediated gene therapy for hemophilia" 1 : 301-315, 2001

      2 Zelechowska MG, "Ultrastructural localization of factor VIII procoagulant antigen in human liver hepatocytes" 317 : 729-730, 1985

      3 Hollestelle MJ, "Tissue distribution of factor VIII gene expression in vivo--a closer look" 86 : 855-861, 2001

      4 Park F, "Therapeutic levels of human factor VIII and IX using HIV-1-based lentiviral vectors in mouse liver" 96 : 1173-1176, 2000

      5 Saenko EL, "The future of recombinant coagulation factors" 1 : 922-930, 2003

      6 Liu L, "Sustained FVIII expression and phenotypic correction of hemophilia A in neonatal mice using an endothelial-targeted sleeping beauty transposon" 13 : 1006-1015, 2006

      7 Bihoreau N, "Structural and functional characterization of Factor VIII-delta II, a new recombinant Factor VIII lacking most of the B-domain" 277 : 23-31, 1991

      8 Ishiwata A, "Phenotype correction of hemophilia A mice with adeno-associated virus vectors carrying the B domain-deleted canine factor VIII gene" 118 : 627-635, 2006

      9 Kang Y, "Persistent expression of factor VIII in vivo following nonprimate lentiviral gene transfer" 106 : 1552-1558, 2005

      10 Zufferey R, "Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo" 15 : 871-875, 1997

      1 VandenDriessche T, "Viral vector-mediated gene therapy for hemophilia" 1 : 301-315, 2001

      2 Zelechowska MG, "Ultrastructural localization of factor VIII procoagulant antigen in human liver hepatocytes" 317 : 729-730, 1985

      3 Hollestelle MJ, "Tissue distribution of factor VIII gene expression in vivo--a closer look" 86 : 855-861, 2001

      4 Park F, "Therapeutic levels of human factor VIII and IX using HIV-1-based lentiviral vectors in mouse liver" 96 : 1173-1176, 2000

      5 Saenko EL, "The future of recombinant coagulation factors" 1 : 922-930, 2003

      6 Liu L, "Sustained FVIII expression and phenotypic correction of hemophilia A in neonatal mice using an endothelial-targeted sleeping beauty transposon" 13 : 1006-1015, 2006

      7 Bihoreau N, "Structural and functional characterization of Factor VIII-delta II, a new recombinant Factor VIII lacking most of the B-domain" 277 : 23-31, 1991

      8 Ishiwata A, "Phenotype correction of hemophilia A mice with adeno-associated virus vectors carrying the B domain-deleted canine factor VIII gene" 118 : 627-635, 2006

      9 Kang Y, "Persistent expression of factor VIII in vivo following nonprimate lentiviral gene transfer" 106 : 1552-1558, 2005

      10 Zufferey R, "Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo" 15 : 871-875, 1997

      11 Kreuz W, "Inhibitor development in previously untreated patients with hemophilia A: a prospective long-term follow-up comparing plasma-derived and recombinant products" 28 : 285-290, 2002

      12 Shi Q, "Factor VIII ectopically targeted to platelets is therapeutic in hemophilia A with high-titer inhibitory antibodies" 116 : 1974-1982, 2006

      13 Ogata K, "Expression of human coagulation factor VIII in adipocytes transduced with the simian immunodeficiency virus agm TYO1-based vector for hemophilia A gene therapy" 11 : 253-259, 2004

      14 Do H, "Expression of factor VIII by murine liver sinusoidal endothelial cells" 274 : 19587-19592, 1999

      15 Park F, "Efficient lentiviral transduction of liver requires cell cycling in vivo" 24 : 49-52, 2000

      16 Wion KL, "Distribution of factor VIII mRNA and antigen in human liver and other tissues" 317 : 726-729, 1985

      17 Moayeri M, "Correction of murine hemophilia A by hematopoietic stem cell gene therapy" 12 : 1034-1042, 2005

      18 Oh TK, "Correction of anemia in uremic rats by intramuscular injection of lentivirus carrying an erythropoietin gene" 26 : 326-334, 2006

      19 Levine P, "Clinical manifestations an therapy of hemophilia A and B. In Hemostasis and Thrombosis. 2nd ed." JB Lippincott 97-111, 1987

      20 Pittman DD, "Biochemical, immunological, and in vivo functional characterization of B-domain-deleted factor VIII" 81 : 2925-2935, 1993

      21 Kaufman RJ, "Advances toward gene therapy for hemophilia at the millennium" 10 : 2091-2107, 1999

      22 Dull T, "A third-generation lentivirus vector with a conditional packaging system" 72 : 8463-8471, 1998

      23 Dull T, "A third generation lentivirus vector with a conditional packaging system" 72 : 8463-8471, 1998

      24 Furie B, "A practical guide to the evaluation and treatment of hemophilia" 84 : 3-9, 1994

      25 Toole JJ, "A large region (approximately equal to 95 kDa) of human factor VIII is dispensable for in vitro procoagulant activity" 83 : 5939-5942, 1986

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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.42 0.3 0.99
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      0.83 0.72 0.546 0.08
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