La dolce vita: fueling chimeric antigen receptor (CAR) T cells with Glut1 to improve therapeutic efficacy
Details
Publication Year 2025-01,Volume 7,Issue #1,Page e00055
Journal Title
Immunometabolism
Publication Type
Commentary
Abstract
The approval of chimeric antigen receptor (CAR) T cell therapies for the treatment of hematological cancers has marked a new era in cancer care, with seven products being FDA approved since 2017. However, challenges remain, and while profound effects are observed initially in myeloma, the majority of patients relapse, which is concomitant with poor CAR T cell persistence. Similarly, the efficacy of CAR T cell therapy is limited in solid tumors, largely due to tumor antigen heterogeneity, immune evasion mechanisms, and poor infiltration and persistence. In this recent study, Guerrero et al endeavor to improve the efficacy of human CAR T cells by overexpressing the glucose transporter GLUT1 and show that GLUT1 overexpressing CAR T cells have improved capacity to persist and control tumor burden in vivo.
Publisher
Wolters Kluwer
Keywords
Glut1; cancer; chimeric antigen receptor T cells; cytokines; glucose; glycolysis; metabolism; tumor
Department(s)
Laboratory Research
Open Access at Publisher's Site
https://doi.org/10.1097/in9.0000000000000055
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2025-01-28 02:47:14
Last Modified: 2025-01-28 02:54:38

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