Chemotherapy and radiotherapy: Cryptic anticancer vaccines

被引:154
作者
Ma, Yuting [2 ,3 ]
Kepp, Oliver [3 ]
Ghiringhelli, Francois [2 ,3 ,4 ,5 ]
Apetoh, Lionel [2 ,3 ]
Aymerica, Laetitia [2 ,3 ]
Locher, Clara [2 ,3 ]
Tesniere, Antoine [3 ]
Martins, Isabelle [3 ]
Ly, Andre [2 ,3 ]
Haynes, Nicole M. [6 ]
Smyth, Mark J. [6 ]
Kroemer, Guido [1 ,3 ]
Zitvogel, Laurence [2 ,3 ]
机构
[1] Inst Gustave Roussy, INSERM, U848, F-94805 Villejuif, France
[2] INSERM, U805, F-94805 Villejuif, France
[3] Univ Paris 11, F-94805 Villejuif, France
[4] INSERM, CRI 866, AVENIR Team, F-21000 Dijon, France
[5] Ctr Georges Francois Leclerc, F-21000 Dijon, France
[6] Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic 3002, Australia
基金
英国医学研究理事会;
关键词
Chemotherapy; Cancer; Inflammasome; Interleukin-1; beta; Interferon-gamma; COLONY-STIMULATING FACTOR; MEDIATED TUMOR DESTRUCTION; LOW-DOSE CYCLOPHOSPHAMIDE; ACUTE MYELOID-LEUKEMIA; AUGMENTS ANTITUMOR IMMUNITY; AUTOLOGOUS MELANOMA-CELLS; HEAT-SHOCK PROTEINS; REGULATORY T-CELLS; DENDRITIC CELLS; APOPTOTIC CELLS;
D O I
10.1016/j.smim.2010.03.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
An attractive, yet hitherto unproven concept predicts that the promotion of tumor regression should elicit the host's immune response against residual tumor cells to achieve an optimal therapeutic effect. In a way, chemo- or radiotherapy must trigger "danger signals" emitted from immunogenic cell death and hence elicit "danger associated molecular patterns" to stimulate powerful anticancer immune responses. Here, based on the recent experimental and clinical evidence, we will discuss the molecular identity of the multiple checkpoints that dictate the success of "immunogenic chemotherapy" at the levels of the drug, of the tumor cell and of the host immune system. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:113 / 124
页数:12
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