Nonviral Transfer of the Gene Encoding Coagulation Factor VIII in Patients with Severe Hemophilia A
David A. Roth, M.D., Nicholas E. Tawa, Jr., M.D., Ph.D., Joanne M. O'Brien, R.N., Douglas A. Treco, Ph.D., Richard F Selden, M.D., Ph.D., for the Factor VIII Transkaryotic Therapy Study Group
Background We tested the safety of a nonviral somatic-cell gene-therapysystem in patients with severe hemophilia A.
Methods An open-label, phase 1 trial was conducted in six patientswith severe hemophilia A. Dermal fibroblasts obtained from eachpatient by skin biopsy were grown in culture and transfectedwith a plasmid containing sequences of the gene that encodesfactor VIII. Cells that produced factor VIII were selected,cloned, and propagated in vitro. The cloned cells were thenharvested and administered to the patients by laparoscopic injectioninto the omentum. The patients were followed for 12 months afterthe implantation of the genetically altered cells. An interimanalysis was performed.
Results There were no serious adverse events related to theuse of factor VIIIproducing fibroblasts or the implantationprocedure. No long-term complications developed, and no inhibitorsof factor VIII were detected. In four of the six patients, plasmalevels of factor VIII activity rose above the levels observedbefore the procedure. The increase in factor VIII activity coincidedwith a decrease in bleeding, a reduction in the use of exogenousfactor VIII, or both. In the patient with the highest levelof factor VIII activity, the clinical changes lasted approximately10 months.
Conclusions Implantation of genetically altered fibroblaststhat produce factor VIII is safe and well tolerated. This formof gene therapy is feasible in patients with severe hemophiliaA.
Source Information
From the Center for Hemostasis and Thrombosis Research, Department of Medicine (D.A.R., J.M.O.), and the Department of Surgery (N.E.T.), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston; and Transkaryotic Therapies, Cambridge, Mass. (D.A.T., R.FS.).
Address reprint requests to Dr. Roth at Beth Israel Deaconess Medical Center, Center for Hemostasis and Thrombosis Research, RE-302, 41 Ave. Louis Pasteur, Boston, MA 02115, or at droth{at}caregroup.harvard.edu.
van den Biggelaar, M., Bouwens, E. A.M., Kootstra, N. A., Hebbel, R. P., Voorberg, J., Mertens, K.
(2009). Storage and regulated secretion of factor VIII in blood outgrowth endothelial cells. haematol
94: 670-678
[Abstract][Full Text]
Xu, D., Alipio, Z., Fink, L. M., Adcock, D. M., Yang, J., Ward, D. C., Ma, Y.
(2009). From the Cover: Phenotypic correction of murine hemophilia A using an iPS cell-based therapy. Proc. Natl. Acad. Sci. USA
106: 808-813
[Abstract][Full Text]
Peng, B., Ye, P., Blazar, B. R., Freeman, G. J., Rawlings, D. J., Ochs, H. D., Miao, C. H.
(2008). Transient blockade of the inducible costimulator pathway generates long-term tolerance to factor VIII after nonviral gene transfer into hemophilia A mice. Blood
112: 1662-1672
[Abstract][Full Text]
High, K. A.
(2007). Update on Progress and Hurdles in Novel Genetic Therapies for Hemophilia. ASH Education Book
2007: 466-472
[Abstract][Full Text]
Spira, J., Plyushch, O. P., Andreeva, T. A., Andreev, Y.
(2006). Prolonged bleeding-free period following prophylactic infusion of recombinant factor VIII reconstituted with pegylated liposomes. Blood
108: 3668-3673
[Abstract][Full Text]
Gangadharan, B., Parker, E. T., Ide, L. M., Spencer, H. T., Doering, C. B.
(2006). High-level expression of porcine factor VIII from genetically modified bone marrow-derived stem cells. Blood
107: 3859-3864
[Abstract][Full Text]
James, P. D., Raut, S., Rivard, G. E., Poon, M.-C., Warner, M., McKenna, S., Leggo, J., Lillicrap, D.
(2005). Aminoglycoside suppression of nonsense mutations in severe hemophilia. Blood
106: 3043-3048
[Abstract][Full Text]
Lippin, Y., Dranitzki-Elhalel, M., Brill-Almon, E., Mei-Zahav, C., Mizrachi, S., Liberman, Y., Iaina, A., Kaplan, E., Podjarny, E., Zeira, E., Harati, M., Casadevall, N., Shani, N., Galun, E.
(2005). Human erythropoietin gene therapy for patients with chronic renal failure. Blood
106: 2280-2286
[Abstract][Full Text]
Xu, L., Nichols, T. C., Sarkar, R., McCorquodale, S., Bellinger, D. A., Ponder, K. P.
(2005). Absence of a desmopressin response after therapeutic expression of factor VIII in hemophilia A dogs with liver-directed neonatal gene therapy. Proc. Natl. Acad. Sci. USA
102: 6080-6085
[Abstract][Full Text]
Schuettrumpf, J., Herzog, R. W., Schlachterman, A., Kaufhold, A., Stafford, D. W., Arruda, V. R.
(2005). Factor IX variants improve gene therapy efficacy for hemophilia B. Blood
105: 2316-2323
[Abstract][Full Text]
Miao, H. Z., Sirachainan, N., Palmer, L., Kucab, P., Cunningham, M. A., Kaufman, R. J., Pipe, S. W.
(2004). Bioengineering of coagulation factor VIII for improved secretion. Blood
103: 3412-3419
[Abstract][Full Text]
Doering, C. B., Healey, J. F., Parker, E. T., Barrow, R. T., Lollar, P.
(2004). Identification of Porcine Coagulation Factor VIII Domains Responsible for High Level Expression via Enhanced Secretion. J. Biol. Chem.
279: 6546-6552
[Abstract][Full Text]
Lillicrap, D.
(2004). Hemophilia gene therapy: it's a matter of expression. Blood
103: 5-6
[Full Text]
Pearson, J. D.
(2003). Using Endothelial Progenitor Cells for Gene Therapy. Arterioscler. Thromb. Vasc. Bio.
23: 2117-2118
[Full Text]
Herder, C., Tonn, T., Oostendorp, R., Becker, S., Keller, U., Peschel, C., Grez, M., Seifried, E.
(2003). Sustained Expansion and Transgene Expression of Coagulation Factor VIII-Transduced Cord Blood-Derived Endothelial Progenitor Cells. Arterioscler. Thromb. Vasc. Bio.
23: 2266-2272
[Abstract][Full Text]
Ponder, K. P.
(2003). Novel therapies for hemophilia A. Blood
102: 3857-3858
[Full Text]
Scallan, C. D., Liu, T., Parker, A. E., Patarroyo-White, S. L., Chen, H., Jiang, H., Vargas, J., Nagy, D., Powell, S. K., Wright, J. F., Sarkar, R., Kazazian, H. H., McClelland, A., Couto, L. B.
(2003). Phenotypic correction of a mouse model of hemophilia A using AAV2 vectors encoding the heavy and light chains of FVIII. Blood
102: 3919-3926
[Abstract][Full Text]
Powell, J. S., Ragni, M. V., White, G. C. II, Lusher, J. M., Hillman-Wiseman, C., Moon, T. E., Cole, V., Ramanathan-Girish, S., Roehl, H., Sajjadi, N., Jolly, D. J., Hurst, D.
(2003). Phase 1 trial of FVIII gene transfer for severe hemophilia A using a retroviral construct administered by peripheral intravenous infusion. Blood
102: 2038-2045
[Abstract][Full Text]
Cooper, R. S., Psaty, B. M.
(2003). Genomics and Medicine: Distraction, Incremental Progress, or the Dawn of a New Age?. ANN INTERN MED
138: 576-580
[Abstract][Full Text]
Rick, M. E., Walsh, C. E., Key, N. S.
(2003). Congenital Bleeding Disorders. ASH Education Book
2003: 559-574
[Abstract][Full Text]
Doering, C. B., Healey, J. F., Parker, E. T., Barrow, R. T., Lollar, P.
(2002). High Level Expression of Recombinant Porcine Coagulation Factor VIII. J. Biol. Chem.
277: 38345-38349
[Abstract][Full Text]
Konetschny, C., Holzer, G. W., Falkner, F. G.
(2002). Retroviral Vectors Produced in the Cytoplasmic Vaccinia Virus System Transduce Intron-Containing Genes. J. Virol.
76: 1236-1243
[Abstract][Full Text]
Lin, Y., Chang, L., Solovey, A., Healey, J. F., Lollar, P., Hebbel, R. P.
(2002). Use of blood outgrowth endothelial cells for gene therapy for hemophilia A. Blood
99: 457-462
[Abstract][Full Text]
Mannucci, P. M.
(2002). Ham-Wasserman Lecture : Hemophilia and Related Bleeding Disorders: A Story of Dismay and Success. ASH Education Book
2002: 1-9
[Abstract][Full Text]
Kim, I.-H., Jozkowicz, A., Piedra, P. A., Oka, K., Chan, L.
(2001). Lifetime correction of genetic deficiency in mice with a single injection of helper-dependent adenoviral vector. Proc. Natl. Acad. Sci. USA
10.1073/pnas.241506298v1
[Abstract][Full Text]
Mannucci, P. M., Tuddenham, E. G.D.
(2001). The Hemophilias -- From Royal Genes to Gene Therapy. NEJM
344: 1773-1779
[Full Text]
Miller, D. G., Stamatoyannopoulos, G.
(2001). Gene Therapy for Hemophilia. NEJM
344: 1782-1784
[Full Text]
Kim, I.-H., Jozkowicz, A., Piedra, P. A., Oka, K., Chan, L.
(2001). Lifetime correction of genetic deficiency in mice with a single injection of helper-dependent adenoviral vector. Proc. Natl. Acad. Sci. USA
98: 13282-13287
[Abstract][Full Text]