一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Unraveling the mechanism of alkaloids from Sophora alopecuroides Linn combined with immune checkpoint blockade in the treatment of non-small cell lung cancer based on systems pharmacology.
Unraveling the mechanism of alkaloids from Sophora alopecuroides Linn combined with immune checkpoint blockade in the treatment of non-small cell lung cancer based on systems pharmacology.
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喹诺里西啶生物碱作为从苦豆子(Sophora alopecuroides Linn,SAL)中提取的重要活性成分,已被证明在包括非小细胞肺癌(NSCLC)在内的多种癌症中具有药理活性。
然而,这些生物碱与免疫检查点阻断(ICB)联合治疗NSCLC是否具有实质性获益尚不清楚。在此,我们基于系统药理学和生物信息学方法,探索这些生物碱与ICB治疗联合应用的潜力。
我们发现SAL中的37种生物碱在分子骨架、药理特性和靶点方面具有高度相似的特征。这些生物碱靶点的表达与NSCLC中TIL(肿瘤浸润淋巴细胞)的浸润水平及多个免疫检查点的表达水平显著相关。它们在抗肿瘤免疫中共享相似的分子机制。苦参碱(Sophocarpine,Sop)是这些生物碱中最具代表性的成分之一。
我们证明Sop通过ADORA1-ATF3轴促进PD-L1表达,从而改善PD-L1阻断治疗的效果。总之,我们的研究确定这些生物碱是治疗NSCLC的有前景的候选药物,无论是单独使用还是与ICB联合使用,均具有药物开发潜力,并可能为改善NSCLC患者的生存提供有前景的策略。
Quinolizidine alkaloids, as essential active ingredients extracted from Sophora alopecuroides Linn (SAL), have been proven to be pharmacologically active in a variety of cancers including non-small cell lung cancer (NSCLC).
However, whether these alkaloids have substantial benefits in combination with immune checkpoint blockade (ICB) for the treatment of NSCLC is unknown.
Here, we explore the potential of these alkaloids in combination with ICB therapy based on a systems pharmacology and bioinformatics approach.
We found that 37 alkaloids in SAL have highly similar characteristics in the molecular skeleton, pharmacological properties, and targets. The expression of targets of these alkaloids are significantly correlated with the infiltration level of tumor infiltrating lymphocytes and the expression levels of multiple immune checkpoints in NSCLC. They share similar molecular mechanisms in antitumor immunity. Sophocarpine (Sop) is one of the most representative constituents of these alkaloids.
We demonstrated that the Sop promotes PD-L1 expression to improve the effects of PD-L1 blockade treatment via the ADORA1-ATF3 axis.
In conclusion, our study identified these alkaloids as promising candidates for the treatment of NSCLC, either alone or in combination with ICB, with potential value for drug development and may provide a promising strategy for improving the survival of NSCLC patients.
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