Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 May:196:76-98.
doi: 10.1016/j.brainresbull.2023.02.014. Epub 2023 Feb 23.

CAR T-cells to treat brain tumors

Affiliations
Free article
Review

CAR T-cells to treat brain tumors

Grace Guzman et al. Brain Res Bull. 2023 May.
Free article

Abstract

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 glioblastoma, 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.

Keywords: Chimeric antigen receptor; Glioblastoma; Pediatric brain tumor; Pediatric glioma; Preclinical brain tumor models; T-cell.

PubMed Disclaimer

Conflict of interest statement

Declaration of Competing Interest None.

Publication types

Substances

LinkOut - more resources