嵌合抗原受体
实体瘤
淋巴瘤
癌症研究
CD19
医学
免疫疗法
肿瘤微环境
T细胞
细胞疗法
免疫系统
免疫学
白血病
细胞
癌症
生物
内科学
遗传学
作者
Lihong Wang,Lufang Zhang,Wei Ma,Yang Yang Wang,Zaiwen Fan,Zhenguo Cheng,Yaohe Wang
出处
期刊:Cancer Letters
[Elsevier]
日期:2024-04-10
卷期号:591: 216871-216871
被引量:7
标识
DOI:10.1016/j.canlet.2024.216871
摘要
Chimeric antigen receptor T (CAR-T) cell therapy, as an adoptive immunotherapy, is playing an increasingly important role in the treatment of malignant tumors. CAR-T cells are referred to as "living drugs" as they not only target tumor cells directly, but also induce long-term immune memory that has the potential to provide long-lasting protection. CD19.CAR-T cells have achieved complete response rates of over 90 % for acute lymphoblastic leukemia and over 60 % for non-Hodgkin's lymphoma. However, the response rate of CAR-T cells in the treatment of solid tumors remains extremely low and the side effects potentially severe. In this review, we discuss the limitations that the solid tumor microenvironment poses for CAR-T application and the solutions that are being developed to address these limitations, in the hope that in the near future, CAR-T cell therapy for solid tumors can attain the same success rates as are now being seen clinically for hematological malignancies.
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