Current developments in cancer vaccines and cellular immunotherapy

被引:238
作者
Ribas, A
Butterfield, LH
Glaspy, JA
Economou, JS
机构
[1] Univ Calif Los Angeles, Med Ctr, Dept Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Surg Oncol, Div Hematol Oncol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Surg, Div Hematol Oncol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Div Hematol Oncol, Los Angeles, CA 90095 USA
关键词
D O I
10.1200/JCO.2003.06.041
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This article reviews the immunologic basis of clinical trials that test means of tumor antigen recognition and immune activation, with the goal to provide the clinician with a mechanistic understanding of ongoing cancer vaccine and cellular immunotherapy clinical trials. Multiple novel immunotherapy strategies have reached the stage of testing in clinical trials that were accelerated by recent advances in the characterization of tumor antigens and by a more precise knowledge of the regulation of cell-mediated immune responses. The key steps in the generation of an immune response to cancer cells include loading of tumor antigens onto antigen-presenting cells in vitro or in vivo, presenting antigen in the appropriate immune stimulatory environment, activating cytotoxic lymphocytes, and blocking autoregulatory control mechanisms. This knowledge has opened the door to antigen-specific immunization for cancer using tumor-derived proteins or RNA, or synthetically generated peptide epitopes, RNA, or DNA. The critical step of antigen presentation has been facilitated by the coadministration of powerful immunologic adjuvants, the provision of costimulatory molecules and immune stimulatory cytokines, and the ability to culture dendritic cells. Advances in the understanding of the nature of tumor antigens and their optimal presentation, and in the regulatory mechanisms that govern the immune system, have provided multiple novel immunotherapy intervention strategies that are being tested in clinical trials.
引用
收藏
页码:2415 / 2432
页数:18
相关论文
共 132 条
  • [91] Ribas Antoni, 2002, Current Gene Therapy, V2, P57, DOI 10.2174/1566523023348129
  • [92] Riddell SR, 2000, CANCER J, V6, pS250
  • [93] A conditioned dendritic cell can be a temporal bridge between a CD4+ T-helper and a T-killer cell
    Ridge, JP
    Di Rosa, F
    Matzinger, P
    [J]. NATURE, 1998, 393 (6684) : 474 - 478
  • [94] Robertson MJ, 1999, CLIN CANCER RES, V5, P9
  • [95] THE IMMUNOTHERAPY AND GENE-THERAPY OF CANCER
    ROSENBERG, SA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (02) : 180 - 199
  • [96] Progress in human tumour immunology and immunotherapy
    Rosenberg, SA
    [J]. NATURE, 2001, 411 (6835) : 380 - 384
  • [97] Rosenberg SA, 1999, J IMMUNOL, V163, P1690
  • [98] Immunologic and therapeutic evaluation of a synthetic peptide vaccine for the treatment of patients with metastatic melanoma
    Rosenberg, SA
    Yang, JC
    Schwartzentruber, DJ
    Hwu, P
    Marincola, FM
    Topalian, SL
    Restifo, NP
    Dudley, ME
    Schwarz, SL
    Spiess, PJ
    Wunderlich, JR
    Parkhurst, MR
    Kawakami, Y
    Seipp, CA
    Einhorn, JH
    White, DE
    [J]. NATURE MEDICINE, 1998, 4 (03) : 321 - 327
  • [99] Immunizing patients with metastatic melanoma using recombinant adenoviruses encoding MART-1 or gp100 melanoma antigens
    Rosenberg, SA
    Zhai, YF
    Yang, JC
    Schwartzentruber, DJ
    Hwu, P
    Marincola, F
    Topalian, SL
    Restifo, NP
    Seipp, CA
    Einhorn, JH
    Roberts, B
    White, DE
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (24) : 1894 - 1900
  • [100] TREATMENT OF PATIENTS WITH METASTATIC MELANOMA WITH AUTOLOGOUS TUMOR-INFILTRATING LYMPHOCYTES AND INTERLEUKIN-2
    ROSENBERG, SA
    YANNELLI, JR
    YANG, JC
    TOPALIAN, SL
    SCHWARTZENTRUBER, DJ
    WEBER, JS
    PARKINSON, DR
    SEIPP, CA
    EINHORN, JN
    WHITE, DE
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (15) : 1159 - 1166