CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Transcription factors in chimeric antigen receptor T-cell development.
Transcription factors in chimeric antigen receptor T-cell development.
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嵌合抗原受体(CAR)T细胞疗法是一种创新的癌症治疗方法,在淋巴瘤治疗中显示出良好的效果。然而,研究发现其在实体瘤治疗中效果较差。为克服这一局限,研究人员探索了将CAR-T 疗法与靶向特定基因或生物标志物的其他互补方案联合使用,以增强协同治疗效果。转录因子(TFs)已被确定为潜在标志物,可调控CAR-T 细胞中的基因表达,从而增强其细胞毒性和安全性。已知TFs能特异性结合DNA并招募辅因子蛋白来调控靶基因的表达。通过靶向TFs,可以改变CAR-T 细胞的表型和转录图谱,从而提高其效应功能,例如减少耗竭、增强CAR-T 细胞的存活和细胞毒性,进而改善其抗肿瘤反应。本综述总结了转录因子在CAR-T 疗法中的应用,以增强CAR-T 细胞在实体瘤治疗中的协同治疗效果并改善其抗肿瘤反应。
Chimeric antigen receptor (CAR) T-cell therapy is a new and innovative approach to treating cancers that has shown promising results in the treatment of lymphoma.
However, it has been found to be less effective in the treatment of solid tumors. To overcome the limitation, researchers have explored the use of combined CAR-T therapy with other complementary regimens that target specific genes or biomarkers, which would enhance the synergistic therapeutic effects. Transcription factors (TFs) have been identified as potential markers that can regulate gene expression in CAR-T cells to enhance their cytotoxicity and safety. TFs are known to bind DNA specifically and recruit cofactor proteins to regulate the expression of target genes.
By targeting TFs, it is possible to improve the anti-tumor response of CAR-T cells by altering their phenotype and transcriptional map, thereby increasing their effector function, such as reducing the exhaustion, enhancing the survival, and cytotoxicity of CAR-T cells. This review summarizes the application of transcription factors in CART therapy to enhance the synergistic therapeutic effect of CAR-T cells in the treatment of solid tumors and improve their anti-tumor responses.
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