Immune checkpoint inhibitors: new strategies to checkmate cancer

被引:57
作者
Wilson, R. A. M. [1 ]
Evans, T. R. J. [2 ,3 ]
Fraser, A. R. [1 ,4 ]
Nibbs, R. J. B. [1 ]
机构
[1] Univ Glasgow, Inst Infect Immun & Inflammat, Glasgow, Lanark, Scotland
[2] Canc Res UK Beatson Inst, Glasgow, Lanark, Scotland
[3] Univ Glasgow, Inst Canc Sci, Glasgow, Lanark, Scotland
[4] Scottish Natl Blood Transfus Serv, Adv Therapeut, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
antibodies; cancer; T cell; tumour immunology; CELL LUNG-CANCER; REGULATORY T-CELLS; RANDOMIZED CONTROLLED-TRIAL; NIVOLUMAB PLUS IPILIMUMAB; ADVANCED MELANOMA; OPEN-LABEL; METASTATIC MELANOMA; PD-1; BLOCKADE; PHASE-2; TRIAL; DOUBLE-BLIND;
D O I
10.1111/cei.13081
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immune checkpoint inhibitors (ICIs) targeting cytotoxic T lymphocyte-associated protein-4 (CTLA-4) or programmed cell death protein 1 (PD-1) receptors have demonstrated remarkable efficacy in subsets of patients with malignant disease. This emerging treatment modality holds great promise for future cancer treatment and has engaged pharmaceutical research interests in tumour immunology. While ICIs can induce rapid and durable responses in some patients, identifying predictive factors for effective clinical responses has proved challenging. This review summarizes the mechanisms of action of ICIs and outlines important preclinical work that contributed to their development. We explore clinical data that has led to disease-specific drug licensing, and highlight key clinical trials that have revealed ICI efficacy across a range of malignancies. We describe how ICIs have been used as part of combination therapies, and explore their future prospects in this area. We conclude by discussing the incorporation of these new immunotherapeutics into precision approaches to cancer therapy.
引用
收藏
页码:133 / 148
页数:16
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