Desirable cell death during anticancer chemotherapy

被引:62
作者
Locher, Clara [1 ,2 ,3 ]
Conforti, Rosa [1 ]
Aymeric, Laetitia [1 ,2 ]
Ma, Yuting [1 ,2 ]
Yamazaki, Takahiro [1 ]
Rusakiewicz, Sylvie [1 ,2 ]
Tesniere, Antoine [4 ]
Ghiringhelli, Francois [5 ,6 ]
Apetoh, Lionel [1 ,2 ]
Morel, Yannis [7 ]
Girard, Jean-Philippe [8 ,9 ]
Kroemer, Guido [4 ,10 ,11 ,12 ]
Zitvogel, Laurence [1 ,2 ,3 ]
机构
[1] Inst Gustave Roussy, INSERM, U1015, F-94805 Villejuif, France
[2] Univ Paris 11, Villejuif, France
[3] INSERM, CIC BT507, Villejuif, France
[4] INSERM, U848, Villejuif, France
[5] INSERM, AVENIR Team, Dijon, France
[6] Ctr Georges Francois Leclerc, Dijon, France
[7] Innate Pharma, Marseille, France
[8] IPBS, CNRS, Toulouse, France
[9] Univ Toulouse, UPS, IPBS, Toulouse, France
[10] Ctr Rech Cordeliers, Paris, France
[11] Hop Europeen Georges Pompidou, AP HP, Paris, France
[12] Univ Paris 05, Paris, France
来源
CLEARANCE OF DYING CELLS IN HEALTHY AND DISEASED IMMUNE SYSTEMS | 2010年 / 1209卷
关键词
cancer; immunogenic cell death; immunotherapy; chemotherapy; toll-like receptor; TOLL-LIKE RECEPTORS; DENDRITIC CELLS; CALRETICULIN EXPOSURE; INNATE IMMUNITY; CANCER-CELLS; STEM-CELLS; NKT CELLS; T-CELLS; IL-33; CYTOKINE;
D O I
10.1111/j.1749-6632.2010.05763.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The concept of immunogenic chemotherapy that has recently emerged relies upon the capacity of a cytotoxic compound to trigger a cell-death modality. This modality elicits cross-priming by dendritic cells of tumor antigen-specific T cells that will contribute to the tumoricidal activity of the compound and protect the host against relapse. In contrast, most anticancer drugs elicit nonimmunogenic apoptosis that is not accompanied with an immunizing property. This review will discuss some molecular and metabolic changes required at the level of the tumor that must engage key pathways at the level of the host for the induction of Tc1 polarized protective T cell responses during chemotherapy. We will summarize the immune adjuvants that can boost the immunogenicity of cell death to augment the efficacy of chemotherapy.
引用
收藏
页码:99 / 108
页数:10
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