CAR T-cells to treat brain tumors

被引:8
作者
Guzman, Grace [1 ]
Pellot, Karolina [3 ]
Reed, Megan R. [1 ,2 ]
Rodriguez, Analiz [1 ,4 ]
机构
[1] Univ Arkansas Med Sci, Dept Neurosurg, Little Rock, AR USA
[2] Univ Arkansas Med Sci, Dept Biochem & Mol Biol, Little Rock, AR USA
[3] Ponce Hlth Sci Univ, Ponce, PR USA
[4] 4301 W Markham St 507, Little Rock, AR 72205 USA
基金
美国国家卫生研究院;
关键词
Chimeric antigen receptor; T-cell; Glioblastoma; Pediatric brain tumor; Pediatric glioma; Preclinical brain tumor models; CENTRAL-NERVOUS-SYSTEM; BREAST-CANCER METASTASIS; ADOPTIVE IMMUNOTHERAPY; EXTRACELLULAR-MATRIX; MOLECULAR CLASSIFICATION; SUPPRESSOR-CELLS; EPENDYMAL TUMORS; EPHA2; RECEPTOR; PONTINE GLIOMA; B-CELL;
D O I
10.1016/j.brainresbull.2023.02.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tremendous success using CAR T therapy in hematological malignancies has garnered significant interest in developing such treatments for solid tumors, including brain tumors. This success, however, has yet to be mirrored in solid organ neoplasms. CAR T function has shown limited efficacy against brain tumors due to several factors including the immunosuppressive tumor microenvironment, blood-brain barrier, and tumor -antigen heterogeneity. Despite these considerations, CAR T-cell therapy has the potential to be implemented as a treatment modality for brain tumors. Here, we review adult and pediatric brain tumors, including glio-blastoma, diffuse midline gliomas, and medulloblastomas that continue to portend a grim prognosis. We describe insights gained from different preclinical models using CAR T therapy against various brain tumors and results gathered from ongoing clinical trials. Furthermore, we outline the challenges limiting CAR T therapy success against brain tumors and summarize advancements made to overcome these obstacles.
引用
收藏
页码:76 / 98
页数:23
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