CONSIDERATIONS FOR THE USE OF CYTOKINE-SECRETING TUMOR-CELL PREPARATIONS FOR CANCER-TREATMENT

被引:44
作者
VIEWEG, J [1 ]
GILBOA, E [1 ]
机构
[1] DUKE UNIV, MED CTR, DEPT SURG, DIV EXPTL SURG, DURHAM, NC 27710 USA
关键词
D O I
10.3109/07357909509011690
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Limited efficacy of chemotherapy in most solid tumors has revived interest in immunotherapeutic approaches for cancer. One novel form of immunotherapy is the use of cancer vaccines consisting of tumor cells genetically engineered to secrete cytokines. The rationale for this immunization strategy is based on the existence of tumor-specific antigens, on the importance of the cellular arm of the immune system in mediating an effective antitumor response, and on the role of cytokines in regulating the cellular immune response. Such tumor vaccines showed considerable promise in various animal models and induced potent antitumor immunity in the host, which led to regression of established tumors and, moreover, produced immunological memory protecting animals from a subsequent tumor challenge at a distant site. Translated to the human patient, this implies that genetically modified tumor vaccines may be able to eradicate or reduce existing tumor deposits to subclinical levels as well as provide long-term protection from regrowth of tumor cells. This report will review and discuss the concept and rationale for the use of cytokine-secreting tumor vaccines for the treatment of human malignancies.
引用
收藏
页码:193 / 201
页数:9
相关论文
共 66 条
  • [1] ADOPTIVELY TRANSFERRED TUMOR-INFILTRATING LYMPHOCYTES CAN CURE ESTABLISHED METASTATIC TUMOR IN MICE AND PERSIST LONG-TERM INVIVO AS FUNCTIONAL MEMORY LYMPHOCYTES-T
    ALEXANDER, RB
    ROSENBERG, SA
    [J]. JOURNAL OF IMMUNOTHERAPY, 1991, 10 (06): : 389 - 397
  • [2] EXPRESSION OF MURINE INTERLEUKIN-7 IN A MURINE GLIOMA CELL-LINE RESULTS IN REDUCED TUMORIGENICITY INVIVO
    AOKI, T
    TASHIRO, K
    MIYATAKE, S
    KINASHI, T
    NAKANO, T
    ODA, Y
    KIKUCHI, H
    HONJO, T
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (09) : 3850 - 3854
  • [3] ASHER AL, 1991, J IMMUNOL, V146, P3227
  • [4] PARVOVIRUS REPLICATION
    BERNS, KI
    [J]. MICROBIOLOGICAL REVIEWS, 1990, 54 (03) : 316 - 329
  • [5] EPIDEMIOLOGY OF ADENOVIRUS-ASSOCIATED VIRUS INFECTION IN A NURSERY POPULATION
    BLACKLOW, NR
    HOGGAN, MD
    KAPIKIAN, AZ
    AUSTIN, JB
    ROWE, WP
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 1968, 88 (03) : 368 - &
  • [6] TUMOR SUPPRESSION AFTER TUMOR-CELL TARGETED TUMOR-NECROSIS-FACTOR-ALPHA GENE-TRANSFER
    BLANKENSTEIN, T
    QIN, ZH
    UBERLA, K
    MULLER, W
    ROSEN, H
    VOLK, HD
    DIAMANTSTEIN, T
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (05) : 1047 - 1052
  • [7] IMMUNOTHERAPY OF CANCER USING LOCAL-ADMINISTRATION OF LYMPHOID-CELLS TRANSFORMED BY IL-2 CDNA AND CONSTITUTIVELY PRODUCING IL-2
    BUBENIK, J
    SIMOVA, J
    JANDLOVA, T
    [J]. IMMUNOLOGY LETTERS, 1990, 23 (04) : 287 - 292
  • [8] CAVALLO F, 1992, J IMMUNOL, V149, P3627
  • [9] COSTIMULATION OF ANTITUMOR IMMUNITY BY THE B7 COUNTERRECEPTOR FOR THE LYMPHOCYTE-T MOLECULES CD28 AND CTLA-4
    CHEN, LP
    ASHE, S
    BRADY, WA
    HELLSTROM, I
    HELLSTROM, KE
    LEDBETTER, JA
    MCGOWAN, P
    LINSLEY, PS
    [J]. CELL, 1992, 71 (07) : 1093 - 1102
  • [10] GRANULOCYTE COLONY-STIMULATING FACTOR GENE-TRANSFER SUPPRESSES TUMORIGENICITY OF A MURINE ADENOCARCINOMA INVIVO
    COLOMBO, MP
    FERRARI, G
    STOPPACCIARO, A
    PARENZA, M
    RODOLFO, M
    MAVILIO, F
    PARMIANI, G
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (04) : 889 - 897