Immunosuppressive strategies that are mediated by tumor cells

被引:1343
作者
Rabinovich, Gabriel A. [1 ]
Gabrilovich, Dmitry
Sotomayor, Eduardo M.
机构
[1] Univ Buenos Aires, DIv Immunogenet, Hosp Clin Jose San Martin, Buenos Aires, DF, Argentina
[2] Univ S Florida, Dept Interdisciplinary Oncol, H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL 33612 USA
关键词
cancer; immunosuppression; tumor-immune escape;
D O I
10.1146/annurev.immunol.25.022106.141609
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite major advances in understanding the mechanisms leading to tumor immunity, a number of obstacles hinder the successful translation of mechanistic insights into effective tumor immunotherapy. Such obstacles include the ability of tumors to foster a tolerant microenvironment and the activation of a plethora of immunosuppressive mechanisms, which may act in concert to counteract effective immune responses. Here we discuss different strategies employed by tumors to thwart immune responses, including tumor-induced impairment of antigen presentation, the activation of negative costimulatory signals, and the elaboration of immunosuppressive factors. In addition, we underscore the influence of regulatory cell populations that may contribute to this immunosuppressive network; these include regulatory T cells, natural killer T cells, and distinct subsets of immature and mature dendritic cells. The current wealth of preclinical information promises a future scenario in which the synchronized blockade of immunosuppressive mechanisms may be effective in combination with other conventional strategies to overcome immunological tolerance and promote tumor regression.
引用
收藏
页码:267 / 296
页数:30
相关论文
共 177 条
[1]   Cancer-associated MUC1 mucin inhibits human T-cell proliferation, which is reversible by IL-2 [J].
Agrawal, B ;
Krantz, MJ ;
Reddish, MA ;
Longenecker, BM .
NATURE MEDICINE, 1998, 4 (01) :43-49
[2]   TGF-β1 attenuates the acquisition and expression of effector function by tumor antigen-specific human memory CD8 T cells [J].
Ahmadzadeh, M ;
Rosenberg, SA .
JOURNAL OF IMMUNOLOGY, 2005, 174 (09) :5215-5223
[3]   Induction of a CD4+ T regulatory type 1 response by cyclooxygenase-2-overexpressing glioma [J].
Akasaki, Y ;
Liu, G ;
Chung, NHC ;
Ehtesham, M ;
Black, KL ;
Yu, JS .
JOURNAL OF IMMUNOLOGY, 2004, 173 (07) :4352-4359
[4]  
Almand B, 2000, CLIN CANCER RES, V6, P1755
[5]   Increased production of immature myeloid cells in cancer patients: A mechanism of immunosuppression in cancer [J].
Almand, B ;
Clark, JI ;
Nikitina, E ;
van Beynen, J ;
English, NR ;
Knight, SC ;
Carbone, DP ;
Gabrilovich, DI .
JOURNAL OF IMMUNOLOGY, 2001, 166 (01) :678-689
[6]   Induction of lymphocyte apoptosis by tumor cell secretion of FasL-bearing microvesicles [J].
Andreola, G ;
Rivoltini, L ;
Castelli, C ;
Huber, V ;
Perego, P ;
Deho, P ;
Squarcina, P ;
Accornero, P ;
Lozupone, F ;
Lugini, L ;
Stringaro, A ;
Molinari, A ;
Arancia, G ;
Gentile, M ;
Parmiani, G ;
Fais, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (10) :1303-1316
[7]   Immunobiology of dendritic cells [J].
Banchereau, J ;
Briere, F ;
Caux, C ;
Davoust, J ;
Lebecque, S ;
Liu, YT ;
Pulendran, B ;
Palucka, K .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :767-+
[8]   Signaling through OX40 (CD134) breaks peripheral T-cell tolerance [J].
Bansal-Pakala, P ;
Jember, AGH ;
Croft, M .
NATURE MEDICINE, 2001, 7 (08) :907-912
[9]   Restoring function in exhausted CD8 T cells during chronic viral infection [J].
Barber, DL ;
Wherry, EJ ;
Masopust, D ;
Zhu, BG ;
Allison, JP ;
Sharpe, AH ;
Freeman, GJ ;
Ahmed, R .
NATURE, 2006, 439 (7077) :682-687
[10]   The CD8α+ dendritic cell is responsible for inducing peripheral self-tolerance to tissue-associated antigens [J].
Belz, GT ;
Behrens, GMN ;
Smith, CM ;
Miller, JFAP ;
Jones, C ;
Lejon, K ;
Fathman, CG ;
Mueller, SN ;
Shortman, K ;
Carbone, FR ;
Heath, WR .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (08) :1099-1104