Approaches to treat immune hot, altered and cold tumours with combination immunotherapies

被引:2853
作者
Galon, Jerome [1 ]
Bruni, Daniela [1 ]
机构
[1] Univ Paris Diderot, Univ Paris Descartes, Sorbonne Univ,Ctr Rech Cordeliers, INSERM,Lab Integrat Canc Immunol,Sorbonne Paris C, Paris, France
基金
欧盟地平线“2020”;
关键词
IMMUNOGENIC CELL-DEATH; CD8; T-CELLS; CHECKPOINT BLOCKADE; DENDRITIC CELLS; PD-1; BLOCKADE; IFN-GAMMA; TGF-BETA; CANCER PROGRESSION; COLORECTAL-CANCER; SUPPRESSOR-CELLS;
D O I
10.1038/s41573-018-0007-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Immunotherapies are the most rapidly growing drug class and have a major impact in oncology and on human health. It is increasingly clear that the effectiveness of immunomodulatory strategies depends on the presence of a baseline immune response and on unleashing of pre-existing immunity. Therefore, a general consensus emerged on the central part played by effector T cells in the antitumour responses. Recent technological, analytical and mechanistic advances in immunology have enabled the identification of patients who are more likely to respond to immunotherapy. In this Review, we focus on defining hot, altered and cold tumours, the complexity of the tumour microenvironment, the Immunoscore and immune contexture of tumours, and we describe approaches to treat such tumours with combination immunotherapies, including checkpoint inhibitors. In the upcoming era of combination immunotherapy, it is becoming critical to understand the mechanisms responsible for hot, altered or cold immune tumours in order to boost a weak antitumour immunity. The impact of combination therapy on the immune response to convert an immune cold into a hot tumour will be discussed.
引用
收藏
页码:197 / 218
页数:22
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