汽车T细胞治疗
抗原
免疫学
医学
神经科学
嵌合抗原受体
T细胞
生物
免疫系统
作者
Haolong Lin,Xiuxiu Yang,Shanwei Ye,Liang Huang,Wei Mu
标识
DOI:10.1016/j.biopha.2024.117252
摘要
Chimeric antigen receptor T (CAR-T) cell therapy has shown promise in treating hematological malignancies and certain solid tumors. However, its efficacy is often hindered by negative relapses resulting from antigen escape. This review firstly elucidates the mechanisms underlying antigen escape during CAR-T cell therapy, including the enrichment of pre-existing target-negative tumor clones, antigen gene mutations or alternative splicing, deficits in antigen processing, antigen redistribution, lineage switch, epitope masking, and trogocytosis-mediated antigen loss. Furthermore, we summarize various strategies to overcome antigen escape, evaluate their advantages and limitations, and propose future research directions. Thus, we aim to provide valuable insights to enhance the effectiveness of CAR-T cell therapy.
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