Experimental vaccine strategies for cancer immunotherapy

被引:82
作者
Chen, CH
Wu, TC
机构
[1] Natl Taiwan Univ Hosp, Coll Med, Dept Internal Med, Taipei, Taiwan
[2] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD USA
[3] Johns Hopkins Med Inst, Dept Oncol, Baltimore, MD USA
[4] Johns Hopkins Med Inst, Dept Obstet & Gynecol, Baltimore, MD USA
[5] Johns Hopkins Med Inst, Dept Mol Microbiol & Immunol, Baltimore, MD USA
关键词
tumor immunology; cancer; vaccine; immunotherapy; antigen; cytotoxic T lymphocyte; dendritic cell;
D O I
10.1007/BF02255855
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recently, cancer immunotherapy has emerged as a therapeutic option for the management of cancer patients. This is based on the fact that our immune system, once activated, is capable of developing specific immunity against neoplastic but not normal cells. Increasing evidence suggests that cell-mediated immunity, particularly T-cell-mediated immunity, is important for the control of tumor cells. Several experimental vaccine strategies have been developed to enhance cell-mediated immunity against tumors. Some of these tumor vaccines have generated promising results in murine tumor systems. In addition, several phase I/II clinical trials using these vaccine strategies have shown extremely encouraging results in patients. In this review, we will discuss many of these promising cancer vaccine strategies. We will pay particular attention to the strategies employing dendritic cells, the central player for tumor vaccine development.
引用
收藏
页码:231 / 252
页数:22
相关论文
共 187 条
  • [21] GM-CSF AND TNF-ALPHA COOPERATE IN THE GENERATION OF DENDRITIC LANGERHANS CELLS
    CAUX, C
    DEZUTTERDAMBUYANT, C
    SCHMITT, D
    BANCHEREAU, J
    [J]. NATURE, 1992, 360 (6401) : 258 - 261
  • [22] Origin, maturation and antigen presenting function of dendritic cells
    Cella, M
    Sallusto, F
    Lanzavecchia, A
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) : 10 - 16
  • [23] Inflammatory stimuli induce accumulation of MHC class II complexes on dendritic cells
    Cella, M
    Engering, A
    Pinet, V
    Pieters, J
    Lanzavecchia, A
    [J]. NATURE, 1997, 388 (6644) : 782 - 787
  • [24] Chamberlain RS, 1996, CANCER RES, V56, P2832
  • [25] Chen KY, 1997, CANCER RES, V57, P3511
  • [26] Chen L, 1997, J IMMUNOL, V159, P351
  • [27] 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
  • [28] Chen PW, 1996, J IMMUNOL, V156, P224
  • [29] CHEN TT, 1994, J IMMUNOL, V153, P4775
  • [30] Chow YH, 1998, J IMMUNOL, V160, P1320