-
1
-
-
0035778751
-
Gene therapy: promises and problems
-
Pfeifer A., Verma I.M. Gene therapy: promises and problems. Annu Rev Genom Hum G 2001, 2:177-211.
-
(2001)
Annu Rev Genom Hum G
, vol.2
, pp. 177-211
-
-
Pfeifer, A.1
Verma, I.M.2
-
2
-
-
0029996147
-
In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector
-
Naldini L., Blomer U., Gallay P., Ory D., Mulligan R., Gage F.H., et al. In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 1996, 272:263-267.
-
(1996)
Science
, vol.272
, pp. 263-267
-
-
Naldini, L.1
Blomer, U.2
Gallay, P.3
Ory, D.4
Mulligan, R.5
Gage, F.H.6
-
4
-
-
0032546352
-
Dendritic cells and the control of immunity
-
Banchereau J., Steinman R.M. Dendritic cells and the control of immunity. Nature 1998, 392:245-252.
-
(1998)
Nature
, vol.392
, pp. 245-252
-
-
Banchereau, J.1
Steinman, R.M.2
-
5
-
-
2442647551
-
Dendritic cell immunotherapy: mapping the way
-
Figdor C.G., de Vries I.J.M., Lesterhuis W.J., Melief C.J.M. Dendritic cell immunotherapy: mapping the way. Nat Med 2004, 10:475-480.
-
(2004)
Nat Med
, vol.10
, pp. 475-480
-
-
Figdor, C.G.1
de Vries, I.J.M.2
Lesterhuis, W.J.3
Melief, C.J.M.4
-
6
-
-
34848837386
-
Taking dendritic cells into medicine
-
Steinman R.M., Banchereau J. Taking dendritic cells into medicine. Nature 2007, 449:419-426.
-
(2007)
Nature
, vol.449
, pp. 419-426
-
-
Steinman, R.M.1
Banchereau, J.2
-
7
-
-
31644438572
-
From pathogen to medicine: HIV-1-derived lentiviral vectors as vehicles for dendritic cell based cancer immunotherapy
-
Dullaers M., Thielemans K. From pathogen to medicine: HIV-1-derived lentiviral vectors as vehicles for dendritic cell based cancer immunotherapy. J Gene Med 2006, 8:3-17.
-
(2006)
J Gene Med
, vol.8
, pp. 3-17
-
-
Dullaers, M.1
Thielemans, K.2
-
8
-
-
1542740102
-
Lentiviral transduction of human dendritic cells
-
Schroers R., Chen S.Y. Lentiviral transduction of human dendritic cells. Methods Mol Biol 2004, 246:451-459.
-
(2004)
Methods Mol Biol
, vol.246
, pp. 451-459
-
-
Schroers, R.1
Chen, S.Y.2
-
9
-
-
0036288752
-
Efficient transduction of dendritic cells and induction of a T-cell response by third-generation lentivectors
-
Esslinger C., Romero P., MacDonald H.R. Efficient transduction of dendritic cells and induction of a T-cell response by third-generation lentivectors. Hum Gene Ther 2002, 13:1091-1100.
-
(2002)
Hum Gene Ther
, vol.13
, pp. 1091-1100
-
-
Esslinger, C.1
Romero, P.2
MacDonald, H.R.3
-
10
-
-
27744484813
-
Induction of therapeutic antitumor immunity by in vivo administration of a lentiviral vaccine
-
Kim J.H., Majumder N., Lin H., Watkins S., Falo L.D., You Z. Induction of therapeutic antitumor immunity by in vivo administration of a lentiviral vaccine. Hum Gene Ther 2005, 16:1255-1266.
-
(2005)
Hum Gene Ther
, vol.16
, pp. 1255-1266
-
-
Kim, J.H.1
Majumder, N.2
Lin, H.3
Watkins, S.4
Falo, L.D.5
You, Z.6
-
11
-
-
33645098473
-
Induction of effective therapeutic antitumor immunity by direct in vivo administration of lentiviral vectors
-
Dullaers M., Van Meirvenne S., Heirman C., Straetman L., Bonehill A., Aerts J.L., et al. Induction of effective therapeutic antitumor immunity by direct in vivo administration of lentiviral vectors. Gene Ther 2006, 13:630-640.
-
(2006)
Gene Ther
, vol.13
, pp. 630-640
-
-
Dullaers, M.1
Van Meirvenne, S.2
Heirman, C.3
Straetman, L.4
Bonehill, A.5
Aerts, J.L.6
-
12
-
-
67349173943
-
Lentiviral vectors for HIV disease prevention and treatment
-
Lemiale F., Korokhov N. Lentiviral vectors for HIV disease prevention and treatment. Vaccine 2009, 27:3443-3449.
-
(2009)
Vaccine
, vol.27
, pp. 3443-3449
-
-
Lemiale, F.1
Korokhov, N.2
-
13
-
-
40449116336
-
Engineered lentivector targeting of dendritic cells for in vivo immunization
-
Yang L., Yang H., Rideout K., Cho T., Joo K.I., Ziegler L., et al. Engineered lentivector targeting of dendritic cells for in vivo immunization. Nat Biotechnol 2008, 26:326-334.
-
(2008)
Nat Biotechnol
, vol.26
, pp. 326-334
-
-
Yang, L.1
Yang, H.2
Rideout, K.3
Cho, T.4
Joo, K.I.5
Ziegler, L.6
-
14
-
-
33745108790
-
Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration
-
Montini E., Cesana D., Schmidt M., Sanvito F., Ponzoni M., Bartholomae C., et al. Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration. Nat Biotechnol 2006, 24:687-696.
-
(2006)
Nat Biotechnol
, vol.24
, pp. 687-696
-
-
Montini, E.1
Cesana, D.2
Schmidt, M.3
Sanvito, F.4
Ponzoni, M.5
Bartholomae, C.6
-
15
-
-
58149386433
-
Insertional gene activation by lentiviral and gammaretroviral vectors
-
Bokhoven M., Stephen S.L., Knight S., Gevers E.F., Robinson I.C., Takeuchi Y., et al. Insertional gene activation by lentiviral and gammaretroviral vectors. J Virol 2009, 83:283-294.
-
(2009)
J Virol
, vol.83
, pp. 283-294
-
-
Bokhoven, M.1
Stephen, S.L.2
Knight, S.3
Gevers, E.F.4
Robinson, I.C.5
Takeuchi, Y.6
-
16
-
-
0142084745
-
LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1
-
Hacein-Bey-Abina S., Von Kalle C., Schmidt M., McCormack M.P., Wulffraat N., Leboulch P., et al. LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1. Science 2003, 302:415-419.
-
(2003)
Science
, vol.302
, pp. 415-419
-
-
Hacein-Bey-Abina, S.1
Von Kalle, C.2
Schmidt, M.3
McCormack, M.P.4
Wulffraat, N.5
Leboulch, P.6
-
17
-
-
33646887376
-
Genotoxicity of retroviral integration in hematopoietic cells
-
Nienhuis A.W., Dunbar C.E., Sorrentino B.P. Genotoxicity of retroviral integration in hematopoietic cells. Mol Ther 2006, 13:1031-1049.
-
(2006)
Mol Ther
, vol.13
, pp. 1031-1049
-
-
Nienhuis, A.W.1
Dunbar, C.E.2
Sorrentino, B.P.3
-
18
-
-
68249112926
-
Integration-deficient lentiviral vectors: a slow coming of age
-
Wanisch K., Yanez-Munoz R.J. Integration-deficient lentiviral vectors: a slow coming of age. Mol Ther 2009, 17:1316-1332.
-
(2009)
Mol Ther
, vol.17
, pp. 1316-1332
-
-
Wanisch, K.1
Yanez-Munoz, R.J.2
-
19
-
-
34447134838
-
Use of nonintegrating lentiviral vectors for gene therapy
-
Philpott N.J., Thrasher A.J. Use of nonintegrating lentiviral vectors for gene therapy. Hum Gene Ther 2007, 18:483-489.
-
(2007)
Hum Gene Ther
, vol.18
, pp. 483-489
-
-
Philpott, N.J.1
Thrasher, A.J.2
-
20
-
-
33845187432
-
Lentiviral vectors with a defective integrase allow efficient and sustained transgene expression in vitro and in vivo
-
Philippe S., Sarkis C., Barkats M., Mammeri H., Ladroue C., Petit C., et al. Lentiviral vectors with a defective integrase allow efficient and sustained transgene expression in vitro and in vivo. Proc Natl Acad Sci USA 2006, 103:17684-17689.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 17684-17689
-
-
Philippe, S.1
Sarkis, C.2
Barkats, M.3
Mammeri, H.4
Ladroue, C.5
Petit, C.6
-
21
-
-
33644822908
-
Effective gene therapy with nonintegrating lentiviral vectors
-
Yanez-Munoz R.J., Balaggan K.S., MacNeil A., Howe S.J., Schmidt M., Smith A.J., et al. Effective gene therapy with nonintegrating lentiviral vectors. Nat Med 2006, 12:348-353.
-
(2006)
Nat Med
, vol.12
, pp. 348-353
-
-
Yanez-Munoz, R.J.1
Balaggan, K.S.2
MacNeil, A.3
Howe, S.J.4
Schmidt, M.5
Smith, A.J.6
-
22
-
-
35548987090
-
Stable gene transfer to muscle using non-integrating lentiviral vectors
-
Apolonia L., Waddington S.N., Fernandes C., Ward N.J., Bouma G., Blundell M.P., et al. Stable gene transfer to muscle using non-integrating lentiviral vectors. Mol Ther 2007, 15:1947-1954.
-
(2007)
Mol Ther
, vol.15
, pp. 1947-1954
-
-
Apolonia, L.1
Waddington, S.N.2
Fernandes, C.3
Ward, N.J.4
Bouma, G.5
Blundell, M.P.6
-
23
-
-
56749185598
-
A large U3 deletion causes increased in vivo expression from a nonintegrating lentiviral vector
-
Bayer M., Kantor B., Cockrell A., Ma H., Zeithaml B., Li X., et al. A large U3 deletion causes increased in vivo expression from a nonintegrating lentiviral vector. Mol Ther 2008, 16:1968-1976.
-
(2008)
Mol Ther
, vol.16
, pp. 1968-1976
-
-
Bayer, M.1
Kantor, B.2
Cockrell, A.3
Ma, H.4
Zeithaml, B.5
Li, X.6
-
24
-
-
34548108611
-
Successful immunization with a single injection of non-integrating lentiviral vector
-
Negri D.R., Michelini Z., Baroncelli S., Spada M., Vendetti S., Buffa V., et al. Successful immunization with a single injection of non-integrating lentiviral vector. Mol Ther 2007, 15:1716-1723.
-
(2007)
Mol Ther
, vol.15
, pp. 1716-1723
-
-
Negri, D.R.1
Michelini, Z.2
Baroncelli, S.3
Spada, M.4
Vendetti, S.5
Buffa, V.6
-
25
-
-
58049195710
-
Protective antiviral immunity conferred by a nonintegrative lentiviral vector-based vaccine
-
Coutant F., Frenkiel M.P., Despres P., Charneau P. Protective antiviral immunity conferred by a nonintegrative lentiviral vector-based vaccine. PLoS One 2008, 3:e3973.
-
(2008)
PLoS One
, vol.3
-
-
Coutant, F.1
Frenkiel, M.P.2
Despres, P.3
Charneau, P.4
-
26
-
-
63149089286
-
Nonintegrating lentivector vaccines stimulate prolonged T-cell and antibody responses and are effective in tumor therapy
-
Karwacz K., Mukherjee S., Apolonia L., Blundell M.P., Bouma G., Escors D., et al. Nonintegrating lentivector vaccines stimulate prolonged T-cell and antibody responses and are effective in tumor therapy. J Virol 2009, 83:3094-3103.
-
(2009)
J Virol
, vol.83
, pp. 3094-3103
-
-
Karwacz, K.1
Mukherjee, S.2
Apolonia, L.3
Blundell, M.P.4
Bouma, G.5
Escors, D.6
-
27
-
-
74549131608
-
Nonintegrating lentiviral vectors can effectively deliver ovalbumin antigen for induction of antitumor immunity
-
Hu B., Yang H., Dai B., Tai A., Wang P. Nonintegrating lentiviral vectors can effectively deliver ovalbumin antigen for induction of antitumor immunity. Hum Gene Ther 2009, 20:1652-1664.
-
(2009)
Hum Gene Ther
, vol.20
, pp. 1652-1664
-
-
Hu, B.1
Yang, H.2
Dai, B.3
Tai, A.4
Wang, P.5
-
28
-
-
0030030041
-
Human immunodeficiency virus type 1 integrase mutants retain in vitro integrase activity yet fail to integrate viral DNA efficiently during infection
-
Leavitt A.D., Robles G., Alesandro N., Varmus H.E. Human immunodeficiency virus type 1 integrase mutants retain in vitro integrase activity yet fail to integrate viral DNA efficiently during infection. J Virol 1996, 70:721-728.
-
(1996)
J Virol
, vol.70
, pp. 721-728
-
-
Leavitt, A.D.1
Robles, G.2
Alesandro, N.3
Varmus, H.E.4
-
29
-
-
0036468677
-
Germline transmission and tissue-specific expression of transgenes delivered by lentiviral vectors
-
Lois C., Hong E.J., Pease S., Brown E.J., Baltimore D. Germline transmission and tissue-specific expression of transgenes delivered by lentiviral vectors. Science 2002, 295:868-872.
-
(2002)
Science
, vol.295
, pp. 868-872
-
-
Lois, C.1
Hong, E.J.2
Pease, S.3
Brown, E.J.4
Baltimore, D.5
-
30
-
-
0031710033
-
A third-generation lentivirus vector with a conditional packaging system
-
Dull T., Zufferey R., Kelly M., Mandel R.J., Nguyen M., Trono D., et al. A third-generation lentivirus vector with a conditional packaging system. J Virol 1998, 72:8463-8471.
-
(1998)
J Virol
, vol.72
, pp. 8463-8471
-
-
Dull, T.1
Zufferey, R.2
Kelly, M.3
Mandel, R.J.4
Nguyen, M.5
Trono, D.6
-
31
-
-
33746978775
-
Comparison of lentiviral vector titration methods
-
Geraerts M., Willems S., Baekelandt V., Debyser Z., Gijsbers R. Comparison of lentiviral vector titration methods. BMC Biotechnol 2006, 6:34.
-
(2006)
BMC Biotechnol
, vol.6
, pp. 34
-
-
Geraerts, M.1
Willems, S.2
Baekelandt, V.3
Debyser, Z.4
Gijsbers, R.5
-
32
-
-
0035025888
-
A quantitative assay for HIV DNA integration in vivo
-
Butler S.L., Hansen M.S., Bushman F.D. A quantitative assay for HIV DNA integration in vivo. Nat Med 2001, 7:631-634.
-
(2001)
Nat Med
, vol.7
, pp. 631-634
-
-
Butler, S.L.1
Hansen, M.S.2
Bushman, F.D.3
-
33
-
-
0028178784
-
T cell receptor antagonist peptides induce positive selection
-
Hogquist K.A., Jameson S.C., Heath W.R., Howard J.L., Bevan M.J., Carbone F.R. T cell receptor antagonist peptides induce positive selection. Cell 1994, 76:17-27.
-
(1994)
Cell
, vol.76
, pp. 17-27
-
-
Hogquist, K.A.1
Jameson, S.C.2
Heath, W.R.3
Howard, J.L.4
Bevan, M.J.5
Carbone, F.R.6
-
34
-
-
0031897801
-
Defective TCR expression in transgenic mice constructed using cDNA-based alpha- and beta-chain genes under the control of heterologous regulatory elements
-
Barnden M.J., Allison J., Heath W.R., Carbone F.R. Defective TCR expression in transgenic mice constructed using cDNA-based alpha- and beta-chain genes under the control of heterologous regulatory elements. Immunol Cell Biol 1998, 76:34-40.
-
(1998)
Immunol Cell Biol
, vol.76
, pp. 34-40
-
-
Barnden, M.J.1
Allison, J.2
Heath, W.R.3
Carbone, F.R.4
-
35
-
-
1842686860
-
Novel integrase-defective lentiviral episomal vectors for gene transfer
-
Vargas J., Gusella G.L., Najfeld V., Klotman M.E., Cara A. Novel integrase-defective lentiviral episomal vectors for gene transfer. Hum Gene Ther 2004, 15:361-372.
-
(2004)
Hum Gene Ther
, vol.15
, pp. 361-372
-
-
Vargas, J.1
Gusella, G.L.2
Najfeld, V.3
Klotman, M.E.4
Cara, A.5
-
36
-
-
1542287499
-
Unintegrated lentivirus DNA persistence and accessibility to expression in nondividing cells: analysis with class I integrase mutants
-
Saenz D.T., Loewen N., Peretz M., Whitwam T., Barraza R., Howell K.G., et al. Unintegrated lentivirus DNA persistence and accessibility to expression in nondividing cells: analysis with class I integrase mutants. J Virol 2004, 78:2906-2920.
-
(2004)
J Virol
, vol.78
, pp. 2906-2920
-
-
Saenz, D.T.1
Loewen, N.2
Peretz, M.3
Whitwam, T.4
Barraza, R.5
Howell, K.G.6
-
37
-
-
0036550559
-
Effector and memory T-cell differentiation: implications for vaccine development
-
Kaech S.M., Wherry E.J., Ahmed R. Effector and memory T-cell differentiation: implications for vaccine development. Nat Rev Immunol 2002, 2:251-262.
-
(2002)
Nat Rev Immunol
, vol.2
, pp. 251-262
-
-
Kaech, S.M.1
Wherry, E.J.2
Ahmed, R.3
-
39
-
-
0034151424
-
Immunogene therapy for murine melanoma using recombinant adenoviral vectors expressing melanoma-associated antigens
-
Perricone M.A., Claussen K.A., Smith K.A., Kaplan J.M., Piraino S., Shankara S., et al. Immunogene therapy for murine melanoma using recombinant adenoviral vectors expressing melanoma-associated antigens. Mol Ther 2000, 1:275-284.
-
(2000)
Mol Ther
, vol.1
, pp. 275-284
-
-
Perricone, M.A.1
Claussen, K.A.2
Smith, K.A.3
Kaplan, J.M.4
Piraino, S.5
Shankara, S.6
-
40
-
-
73949111672
-
HIV-1 Gag-specific immunity induced by a lentivector-based vaccine directed to dendritic cells
-
Dai B., Yang L., Yang H., Hu B., Baltimore D., Wang P. HIV-1 Gag-specific immunity induced by a lentivector-based vaccine directed to dendritic cells. Proc Natl Acad Sci USA 2009, 106:20382-20387.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 20382-20387
-
-
Dai, B.1
Yang, L.2
Yang, H.3
Hu, B.4
Baltimore, D.5
Wang, P.6
-
41
-
-
34248208712
-
DC-SIGN and immunoregulation
-
Zhou T., Chen Y., Hao L., Zhang Y. DC-SIGN and immunoregulation. Cell Mol Immunol 2006, 3:279-283.
-
(2006)
Cell Mol Immunol
, vol.3
, pp. 279-283
-
-
Zhou, T.1
Chen, Y.2
Hao, L.3
Zhang, Y.4
-
42
-
-
0029911692
-
A life stage of particle-laden rat dendritic cells in vivo: their terminal division, active phagocytosis, and translocation from the liver to the draining lymph
-
Matsuno K., Ezaki T., Kudo S., Uehara Y. A life stage of particle-laden rat dendritic cells in vivo: their terminal division, active phagocytosis, and translocation from the liver to the draining lymph. J Exp Med 1996, 183:1865-1878.
-
(1996)
J Exp Med
, vol.183
, pp. 1865-1878
-
-
Matsuno, K.1
Ezaki, T.2
Kudo, S.3
Uehara, Y.4
-
43
-
-
0031926091
-
Mutations in the human immunodeficiency virus type 1 integrase D,D(35)E motif do not eliminate provirus formation
-
Gaur M., Leavitt A.D. Mutations in the human immunodeficiency virus type 1 integrase D,D(35)E motif do not eliminate provirus formation. J Virol 1998, 72:4678-4685.
-
(1998)
J Virol
, vol.72
, pp. 4678-4685
-
-
Gaur, M.1
Leavitt, A.D.2
|