IDIOTYPE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR FUSION PROTEIN AS A VACCINE FOR B-CELL LYMPHOMA

被引:276
作者
TAO, MH [1 ]
LEVY, R [1 ]
机构
[1] STANFORD UNIV, MED CTR, SCH MED, DEPT MED, DIV ONCOL, STANFORD, CA 94305 USA
关键词
D O I
10.1038/362755a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To produce a vaccine against cancer, antigens must be found that are preferentially expressed by tumour cells and can induce an immune response against the tumour. The variable regions of the immunoglobulin molecules expressed on malignant B cells (idiotypes) are tumour-specific, but are weak immunogens. To induce an immune response in animals or humans, the idiotypic protein has therefore to be chemically coupled to a strongly immunogenic protein and mixed with an adjuvant1-8. The resulting response can protect animals from subsequent tumour challenge, and cure animals with established tumours in combination with chemotherapy. Granulocyte-macrophage colony-stimulating factor (GM-CSF) augments antigen presentation in a variety of cells9-12. Here we show that by fusing a tumour-derived idiotype to GM-CSF, it can be converted into a strong immunogen capable of inducing idiotype-specific antibodies without other carrier proteins or adjuvants and of protecting recipient animals from challenge with an otherwise lethal dose of tumour cells. This approach may be applicable to the design of vaccines for a variety of other diseases.
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页码:755 / 758
页数:4
相关论文
共 30 条
  • [1] AN ADJUVANT FORMULATION THAT SELECTIVELY ELICITS THE FORMATION OF ANTIBODIES OF PROTECTIVE ISOTYPES AND OF CELL-MEDIATED-IMMUNITY
    ALLISON, AC
    BYARS, NE
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 95 (02) : 157 - 168
  • [2] CHARACTERIZATION OF A CARCINOGEN-INDUCED MURINE B-LYMPHOCYTE CELL LINE OF C3H-EB ORIGIN
    BERGMAN, Y
    HAIMOVICH, J
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1977, 7 (07) : 413 - 417
  • [3] 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
  • [4] CAMPBELL MJ, 1988, J IMMUNOL, V141, P3227
  • [5] CAMPBELL MJ, 1987, J IMMUNOL, V139, P2825
  • [6] ALTERNATIVE V-KAPPA GENE REARRANGEMENTS IN A MURINE B-CELL LYMPHOMA - AN EXPLANATION FOR IDIOTYPIC HETEROGENEITY
    CARROLL, WL
    STARNES, CO
    LEVY, R
    LEVY, S
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (05) : 1607 - 1620
  • [7] ENHANCED HEMATOPOIETIC ACTIVITY OF A HUMAN GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR INTERLEUKIN-3 FUSION PROTEIN
    CURTIS, BM
    WILLIAMS, DE
    BROXMEYER, HE
    DUNN, J
    FARRAH, T
    JEFFERY, E
    CLEVENGER, W
    DEROOS, P
    MARTIN, U
    FRIEND, D
    CRAIG, V
    GAYLE, R
    PRICE, V
    COSMAN, D
    MARCH, CJ
    PARK, LS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (13) : 5809 - 5813
  • [8] INTERLEUKIN-2 PRODUCTION BY TUMOR-CELLS BYPASSES T-HELPER FUNCTION IN THE GENERATION OF AN ANTITUMOR RESPONSE
    FEARON, ER
    PARDOLL, DM
    ITAYA, T
    GOLUMBEK, P
    LEVITSKY, HI
    SIMONS, JW
    KARASUYAMA, H
    VOGELSTEIN, B
    FROST, P
    [J]. CELL, 1990, 60 (03) : 397 - 403
  • [9] FISCHER HG, 1988, J IMMUNOL, V141, P3882
  • [10] TUMOR IMMUNITY INDUCED BY PRE-IMMUNIZATION WITH BALB-C MOUSE MYELOMA PROTEIN
    FREEDMAN, PM
    AUTRY, JR
    TOKUDA, S
    WILLIAMS, RC
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1976, 56 (04) : 735 - 740