Rationally combining immunotherapies to improve efficacy of immune checkpoint blockade in solid tumors

被引:45
|
作者
Dammeijer, Floris [1 ,2 ]
Lau, Sai Ping [2 ,3 ]
van Eijck, Casper H. J. [3 ]
van der Burg, Sjoerd H. [4 ]
Aerts, Joachim G. J. V. [1 ,2 ]
机构
[1] Erasmus MC, Dept Pulm Med, S Gravendijkwal 230, NL-3015 CE Rotterdam, Netherlands
[2] Erasmus MC, Erasmus MC Canc Inst, S Gravendijkwal 230, NL-3015 CE Rotterdam, Netherlands
[3] Erasmus MC, Dept Surg, S Gravendijkwal 230, NL-3015 CE Rotterdam, Netherlands
[4] Leiden Univ, Dept Clin Oncol, Med Ctr, POB 9600, NL-2300 RC Leiden, Netherlands
关键词
Immunotherapy; Immune-checkpoint blockade; Tumor immunology; Tumor microenvironment; Personalized medicine; CELL LUNG-CANCER; REGULATORY T-CELLS; ANTITUMOR IMMUNITY; PD-1; BLOCKADE; PANCREATIC-CARCINOMA; CTLA-4; DENDRITIC CELLS; IFN-GAMMA; NEOANTIGEN LANDSCAPE; ANTI-CTLA-4; THERAPY;
D O I
10.1016/j.cytogfr.2017.06.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
With the widespread application of immune checkpoint blocking antibodies (ICBs) for the treatment of advanced cancer, immunotherapy has proven to be capable of yielding unparalleled clinical results. However, despite the initial success of ICB-treatment, still a minority of patients experience durable responses to ICB therapy. A plethora of mechanisms underlie ICB resistance ranging from low immunogenicity, inadequate generation or recruitment of tumor-specific T cells or local suppression by stromal cells to acquired genetic alterations leading to immune escape. Increasing the response rates to ICBs requires insight into the mechanisms underlying resistance and the subsequent design of rational therapeutic combinations on a per patient basis. In this review, we aim to establish order into the mechanisms governing primary and secondary ICB resistance, offer therapeutic options to circumvent different modes of resistance and plea for a personalized medicine approach to maximize immunotherapeutic benefit for all cancer patients. (C) 2017 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:5 / 15
页数:11
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