4.3 Review

CAR T cells and checkpoint inhibition for the treatment of glioblastoma

期刊

EXPERT OPINION ON BIOLOGICAL THERAPY
卷 20, 期 6, 页码 579-591

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/14712598.2020.1727436

关键词

CAR T cells; exhaustion; solid malignancy; immunotherapy; inhibitory immune checkpoint blockade; Program Death-1 (PD-1); glioblastoma

资金

  1. National Institutes of Health (NIH) National Cancer Institute [P50-CA190991]
  2. NIH National Institute of Neurological Disorders and Stroke [R01-NS099463, R01-NS085412, U01-NS090284]
  3. National Science Foundation

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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.

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