嵌合抗原受体
医学
联合疗法
靶向治疗
T细胞
抗药性
免疫疗法
肿瘤微环境
药理学
免疫学
癌症研究
免疫系统
癌症
内科学
肿瘤细胞
生物
微生物学
作者
Yuxian Huang,Yinjie Qin,Yingzhi He,Dezhi Qiu,Yeqin Zheng,Jiayue Wei,Lenghe Zhang,Dong‐Hua Yang,Yuhua Li
标识
DOI:10.1016/j.drup.2024.101082
摘要
Molecular targeted drugs and chimeric antigen receptor (CAR) T cell therapy represent specific biological treatments that have significantly improved the efficacy of treating hematologic malignancies. However, they face challenges such as drug resistance and recurrence after treatment. Combining molecular targeted drugs and CAR-T cells could regulate immunity, improve tumor microenvironment (TME), promote cell apoptosis, and enhance sensitivity to tumor cell killing. This approach might provide a dual coordinated attack on cancer cells, effectively eliminating minimal residual disease and overcoming therapy resistance. Moreover, molecular targeted drugs can directly or indirectly enhance the anti-tumor effect of CAR-T cells by inducing tumor target antigen expression, reversing CAR-T cell exhaustion, and reducing CAR-T cell associated toxic side effects. Therefore, combining molecular targeted drugs with CAR-T cells is a promising and novel tactic for treating hematologic malignancies. In this review article, we focus on analyzing the mechanism of therapy resistance and its reversal of CAR-T cell therapy resistance, as well as the synergistic mechanism, safety, and future challenges in CAR-T cell therapy in combination with molecular targeted drugs. We aim to explore the benefits of this combination therapy for patients with hematologic malignancies and provide a rationale for subsequent clinical studies.
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