嵌合抗原受体
免疫疗法
T细胞
免疫学
医学
癌症免疫疗法
细胞疗法
癌症研究
T细胞受体
肿瘤微环境
细胞
免疫系统
生物
遗传学
作者
Diana Gumber,Leo David Wang
出处
期刊:EBioMedicine
[Elsevier BV]
日期:2022-03-01
卷期号:77: 103941-103941
被引量:402
标识
DOI:10.1016/j.ebiom.2022.103941
摘要
Chimeric antigen receptor (CAR) T cell therapy has emerged as a cancer treatment with enormous potential, demonstrating impressive antitumor activity in the treatment of hematological malignancies. However, CAR T cell exhaustion is a major limitation to their efficacy, particularly in the application of CAR T cells to solid tumors. CAR T cell exhaustion is thought to be due to persistent antigen stimulation, as well as an immunosuppressive tumor microenvironment, and mitigating exhaustion to maintain CAR T cell effector function and persistence and achieve clinical potency remains a central challenge. Here, we review the underlying mechanisms of exhaustion and discuss emerging strategies to prevent or reverse exhaustion through modifications of the CAR receptor or CAR independent pathways. Additionally, we discuss the potential of these strategies for improving clinical outcomes of CAR T cell therapy.
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