Gene-based cancer vaccines:: an ex vivo approach

被引:29
作者
Van Tendeloo, VFI
Van Broeckhoven, C
Berneman, ZN
机构
[1] Univ Antwerp, Univ Antwerp Hosp, Div Hematol, Lab Expt Hematol, B-2650 Edegem, Belgium
[2] Univ Antwerp VIB, Dept Mol Genet, Mol Genet Lab, Antwerp, Belgium
关键词
cancer immunotherapy; cancer vaccines; gene therapy; gene transfer; dendritic cells; cytotoxic T lymphocytes; tumor-associated antigens; danger theory; immune tolerance; suicide genes; T bodies; cross-priming; tumor vaccines; retroviral vectors; adenoviral vectors; lentiviral vectors; nonviral gene transfer; tumor immunology; tumor rejection antigens;
D O I
10.1038/sj.leu.2402069
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The application of gene transfer techniques to immunotherapy has animated the field of gene-based cancer vaccine research. Gene transfer strategies were developed to bring about active immunization against tumor-associated antigens (TAA) through gene transfer technology. A wide variety of viral and nonviral gene transfer methods have been investigated for immunotherapeutic purposes. Ex vivo strategies include gene delivery into tumor cells and into cellular components of the immune system, including cytotoxic T cells and dendritic cells (DC). The nature of the transferred genetic material as well as the gene transfer method has varied widely depending on the application. Several of these approaches have already been translated into clinical gene therapy trials. In this review, we will focus on the rationale and types of ex vivo gene-based immunotherapy of cancer. Critical areas for future development of gene-based cancer vaccines are addressed, with particular emphasis on use of DC and on the danger-tolerance hypothesis. Finally, the use of gene-modified DC for tumor vaccination and its prospects are discussed.
引用
收藏
页码:545 / 558
页数:14
相关论文
共 201 条
[51]   High efficiency adenovirus-mediated gene transfer to human dendritic cells [J].
Dietz, AB ;
Vuk-Pavlovic, S .
BLOOD, 1998, 91 (02) :392-398
[52]   VACCINATION WITH IRRADIATED TUMOR-CELLS ENGINEERED TO SECRETE MURINE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR STIMULATES POTENT, SPECIFIC, AND LONG-LASTING ANTITUMOR IMMUNITY [J].
DRANOFF, G ;
JAFFEE, E ;
LAZENBY, A ;
GOLUMBEK, P ;
LEVITSKY, H ;
BROSE, K ;
JACKSON, V ;
HAMADA, H ;
PARDOLL, D ;
MULLIGAN, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3539-3543
[53]   Gene immunotherapy in murine acute myeloid leukemia: Granulocyte-macrophage colony-stimulating factor tumor cell vaccines elicit more potent antitumor immunity compared with B7 family and other cytokine vaccines [J].
Dunussi-Joannopoulos, K ;
Dranoff, G ;
Weinstein, HJ ;
Ferrara, JLM ;
Bierer, BE ;
Croop, JM .
BLOOD, 1998, 91 (01) :222-230
[54]  
Dunussi-Joannopoulos Kyriaki, 1999, Blood, V94, P4263
[55]   Gene therapy with B7.1 and GM-CSF vaccines in a murine AML model [J].
DunussiJoannopoulos, K ;
Weinstein, HJ ;
Arceci, RJ ;
Croop, JM .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1997, 19 (06) :536-540
[56]   Irradiated B7-1 transduced primary acute myelogenous leukemia (AML) cells can be used as therapeutic vaccines in murine AML [J].
DunussiJoannopoulos, K ;
Weinstein, HJ ;
Nickerson, PW ;
Strom, TB ;
Burakoff, SJ ;
Croop, JM ;
Arceci, RJ .
BLOOD, 1996, 87 (07) :2938-2946
[57]   The labyrinthine ways of cancer immunotherapy - T cell, tumor cell encounter: "How do I lose thee? Let me count the ways" [J].
Ellem, KAO ;
Schmidt, CW ;
Li, CL ;
Misko, I ;
Kelso, A ;
Sing, G ;
Macdonald, G ;
O'Rourke, MGE .
ADVANCES IN CANCER RESEARCH, VOL 75, 1998, 75 :203-249
[58]   Expression of chimeric granulocyte-macrophage colony-stimulating factor/interleukin 2 receptors in human cytotoxic T lymphocyte clones results in granulocyte-macrophage colony-stimulating factor-dependent growth [J].
Evans, LS ;
Witte, PR ;
Feldhaus, AL ;
Nelson, BH ;
Riddell, SR ;
Greenberg, PD ;
Lupton, SD ;
Jones, LA .
HUMAN GENE THERAPY, 1999, 10 (12) :1941-1951
[59]  
FEARON ER, 1988, CANCER RES, V48, P2975
[60]   INTERLEUKIN-2 PRODUCTION BY TUMOR-CELLS BYPASSES T-HELPER FUNCTION IN THE GENERATION OF AN ANTITUMOR RESPONSE [J].
FEARON, ER ;
PARDOLL, DM ;
ITAYA, T ;
GOLUMBEK, P ;
LEVITSKY, HI ;
SIMONS, JW ;
KARASUYAMA, H ;
VOGELSTEIN, B ;
FROST, P .
CELL, 1990, 60 (03) :397-403