Immune cell profiling in the age of immune checkpoint inhibitors: implications for biomarker discovery and understanding of resistance mechanisms

被引:10
|
作者
Lim, Su Yin [1 ,2 ]
Rizos, Helen [1 ,2 ]
机构
[1] Macquarie Univ, Dept Biomed Sci, Fac Med & Hlth Sci, Sydney, NSW, Australia
[2] Melanoma Inst Australia, Sydney, NSW, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
REGULATORY T-CELLS; LONG-TERM SURVIVAL; PD-1; BLOCKADE; METASTATIC MELANOMA; ADOPTIVE IMMUNOTHERAPY; ACQUIRED-RESISTANCE; COMBINED NIVOLUMAB; PREDICTS RESPONSE; CLINICAL ACTIVITY; CANCER-IMMUNITY;
D O I
10.1007/s00335-018-9757-4
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
Immunotherapy has changed the landscape of cancer treatment. The introduction of immune checkpoint inhibitors has seen tremendous success in improving overall survival of patients with advanced metastatic cancers and has now become the standard of care for multiple tumor types. However, efficacy of immune checkpoint blockade appears to be limited to immunogenic cancers, and even amongst immune-reactive cancers, response rates are low and variable between patients. Recent data have also demonstrated the rapid emergence of resistance to immune checkpoint inhibitors, with some patients progressing on treatment within oneyear. Significant research efforts are now directed at identifying predictive biomarkers and mechanisms of resistance to immune checkpoint blockade. These studies are underpinned by comprehensive and detailed profiling of the immune milieu. In this review, we discuss the utility and efficacy of immune cell profiling to uncover biomarkers of response and mechanisms of resistance to immune checkpoint inhibitors.
引用
收藏
页码:866 / 878
页数:13
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