Molecular mechanism of co-stimulatory domains in promoting CAR-T cell anti-tumor efficacy

[Display omitted] Chimeric antigen receptor (CAR)-engineered T cells have been defined as ‘living drug’. Adding a co-stimulatory domain (CSD) has enhanced the anti-hematological effects of CAR-T cells, thereby elevating their viability for medicinal applications. Various CSDs have helped prepare CAR...

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Veröffentlicht in:Biochemical pharmacology 2024-09, Vol.227, p.116439, Article 116439
Hauptverfasser: Zhao, Wanxin, Yao, Yizhou, Li, Qihong, Xue, Ying, Gao, Xiaoge, Liu, Xiangye, Zhang, Qing, Zheng, Junnian, Sun, Shishuo
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Sprache:eng
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Zusammenfassung:[Display omitted] Chimeric antigen receptor (CAR)-engineered T cells have been defined as ‘living drug’. Adding a co-stimulatory domain (CSD) has enhanced the anti-hematological effects of CAR-T cells, thereby elevating their viability for medicinal applications. Various CSDs have helped prepare CAR-T cells to study anti-tumor efficacy. Previous studies have described and summarized the anti-tumor efficacy of CAR-T cells obtained from different CSDs. However, the underlying molecular mechanisms by which different CSDs affect CAR-T function have been rarely reported. The role of CSDs in T cells has been significantly studied, but whether they can play a unique role as a part of the CAR structure remains undetermined. Here, we summarized the effects of CSDs on CAR-T signaling pathways based on the limited references and speculated the possible mechanism depending on the specific characteristics of CAR-T cells. This review will help understand the molecular mechanism of CSDs in CAR-T cells that exert different anti-tumor effects while providing potential guidance for further interventions to enhance anti-tumor efficacy in immunotherapy.
ISSN:0006-2952
1873-2968
1873-2968
DOI:10.1016/j.bcp.2024.116439