CAR T cells and checkpoint inhibition for the treatment of glioblastoma

被引:38
|
作者
Shen, Steven H. [1 ,2 ,3 ]
Woroniecka, Karolina [1 ,2 ,3 ]
Barbour, Andrew B. [1 ]
Fecci, Peter E. [1 ,2 ,4 ]
Sanchez-Perez, Luis [1 ,2 ,4 ]
Sampson, John H. [1 ,2 ,3 ,4 ]
机构
[1] Duke Univ, Med Ctr, Dept Neurosurg, Duke Brain Tumor Immunotherapy Program, DUMC Box 3050,303 Res Dr,220 Sands Bldg, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Preston Robert Tisch Brain Tumor Ctr, Durham, NC USA
[3] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Neurosurg, Durham, NC USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
CAR T cells; exhaustion; solid malignancy; immunotherapy; inhibitory immune checkpoint blockade; Program Death-1 (PD-1); glioblastoma; TUMOR-INFILTRATING LYMPHOCYTES; STEM-CELLS; MISMATCH REPAIR; RECEPTOR; CANCER; PD-1; IMMUNOTHERAPY; EXHAUSTION; BLOCKADE; GLIOMA;
D O I
10.1080/14712598.2020.1727436
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 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Glioblastoma (GBM) is a highly aggressive brain tumor and is one of the most lethal human cancers. Chimeric antigen receptor (CAR) T cell therapy has markedly improved survival in previously incurable disease; however, this vanguard treatment still faces challenges in GBM. Likewise, checkpoint blockade therapies have not enjoyed the same victories against GBM. As it becomes increasingly evident that a mono-therapeutic approach is unlikely to provide anti-tumor efficacy, there evolves a critical need for combined treatment strategies. Areas covered: This review highlights the clinical successes observed with CAR T cell therapy as well the current efforts to overcome its perceived limitations. The review also explores employed combinations of CAR T cell approaches with immune checkpoint blockade strategies, which aim to potentiate immunotherapeutic benefits while restricting the impact of tumor heterogeneity and T cell exhaustion. Expert opinion: Barriers such as tumor heterogeneity and T cell exhaustion have exposed the weaknesses of various mono-immunotherapeutic approaches to GBM, including CAR T cell and checkpoint blockade strategies. Combining these potentially complementary strategies, however, may proffer a rational means of mitigating these barriers and advancing therapeutic successes against GBM and other solid tumors.
引用
收藏
页码:579 / 591
页数:13
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