Immunosuppressive mechanisms in human tumors: Why we still cannot cure cancer

被引:53
作者
Gross, Stefanie [1 ]
Walden, Peter [1 ]
机构
[1] Humboldt Univ, Dept Dermatol Venerol & Allergy, Charite Univ Med Berlin, Clin Res Grp Tumor Immunol, Charite Pl 1, D-10117 Berlin, Germany
关键词
tumor immunology; T cell; immunosuppression; cancer; Tregs; DC; tumor microenvironment; tumor stroma; tumor angiogenesis; cancer immunotherapy;
D O I
10.1016/j.imlet.2007.11.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tumor cells often evoke specific immune responses that, however, fail to eliminate all the tumor cells. The development of cancer immunotherapies is, therefore, mostly focused on the generation of large numbers of activated anti-tumor effector cells by vaccination or adoptive T cell transfer. These developments are built on an ever-extended list of identified tumor-associated antigens and corresponding T cell epitopes, and a steady flow of reports from proof-of-principle animal model experiments demonstrating cure from disease by immune interventions. However, the promises have not translated into clinical successes for cancer patients. Even where tumor regression or complete responses were achieved there is usually relapse of the disease. Increasing numbers of reports over recent years highlight potential immunosuppressive mechanisms that act in tumors and systemically in cancer patients to block effective anti-tumor immune responses. They account in large parts for the failures of cancer immunotherapy and need to be overcome before progress can be expected. We review here the current state of the research on immunosuppressive networks in human cancer. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 14
页数:8
相关论文
共 108 条
[31]   Immune evasion of tumor cells using membrane-bound complement regulatory proteins [J].
Gorter, A ;
Meri, S .
IMMUNOLOGY TODAY, 1999, 20 (12) :576-582
[32]   The B7 family revisited [J].
Greenwald, RJ ;
Freeman, GJ ;
Sharpe, AH .
ANNUAL REVIEW OF IMMUNOLOGY, 2005, 23 :515-548
[33]   Differential expression of granzymes A and B in human cytotoxic lymphocyte subsets and T regulatory cells [J].
Grossman, WJ ;
Verbsky, JW ;
Tollefsen, BL ;
Kemper, C ;
Atkinson, JP ;
Ley, TJ .
BLOOD, 2004, 104 (09) :2840-2848
[34]   Human T regulatory cells can use the perforin pathway to cause autologous target cell death [J].
Grossman, WJ ;
Verbsky, JW ;
Barchet, W ;
Colonna, M ;
Atkinson, JP ;
Ley, TJ .
IMMUNITY, 2004, 21 (04) :589-601
[35]   Melanoma cell expression of Fas(Apo-1/CD95) ligand: Implications for tumor immune escape [J].
Hahne, M ;
Rimoldi, D ;
Schroter, M ;
Romero, P ;
Schreier, M ;
French, LE ;
Schneider, P ;
Bornand, T ;
Fontana, A ;
Lienard, D ;
Cerottini, JC ;
Tschopp, J .
SCIENCE, 1996, 274 (5291) :1363-1366
[36]   Autocrine secretion of fas ligand shields tumor cells from fas-mediated killing by cytotoxic lymphocytes [J].
Hallermalm, K ;
De Geer, A ;
Kiessling, R ;
Levitsky, V ;
Levitskaya, J .
CANCER RESEARCH, 2004, 64 (18) :6775-6782
[37]   Programmed cell death 1 ligand 1 and tumor-infiltrating CD8+ T lymphocytes are prognostic factors of human ovarian cancer [J].
Hamanishi, Junzo ;
Mandai, Masaki ;
Iwasaki, Masashi ;
Okazaki, Taku ;
Tanaka, Yoshimasa ;
Yamaguchi, Ken ;
Higuchi, Toshihiro ;
Yagi, Haruhiko ;
Takakura, Kenji ;
Minato, Nagahiro ;
Honjo, Tasuku ;
Fujii, Shingo .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (09) :3360-3365
[38]   Shaping of monocyte and macrophage function by adenosine receptors [J].
Hasko, Gyorgy ;
Pacher, Pal ;
Deitch, Edwin A. ;
Vizi, E. Sylvester .
PHARMACOLOGY & THERAPEUTICS, 2007, 113 (02) :264-275
[39]  
Hockel M, 1996, CANCER RES, V56, P4509
[40]   Gr-1+CD115+ immature myeloid suppressor cells mediate the development of tumor-induced T regulatory cells and T-cell anergy in tumor-bearing host [J].
Huang, B ;
Pan, PY ;
Li, QS ;
Sato, AI ;
Levy, DE ;
Bromberg, J ;
Divino, CM ;
Chen, SH .
CANCER RESEARCH, 2006, 66 (02) :1123-1131