克服肿瘤抗原异质性的CAR-T细胞治疗恶性间皮瘤

IF 1.4 Q4 ONCOLOGY
Reena R D'Souza, P. Dimou, Reyisa Bughda, E. Hawkins, Clara Leboreiro Babe, A. Klampatsa
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引用次数: 1

摘要

恶性间皮瘤(MM)是一种罕见的侵袭性实体瘤,治疗选择有限,治疗效果差。免疫治疗在MM中的作用现在已经得到了很好的确立,治疗选择,如检查点抑制剂,正在越来越多地被批准。嵌合抗原受体(CAR)-T细胞治疗已成功地应用于多种血液病,但目前在实体肿瘤中效果不佳,原因包括运输和浸润、有限的T细胞持久性和耗竭、免疫抑制TME和肿瘤抗原异质性等。肿瘤相关抗原(TAAs)在肿瘤细胞上缺乏统一和普遍的表达,以及肿瘤编辑治疗后TAA的异质性,是CAR-T细胞和相关抗原靶向治疗的重要问题。我们的综述讨论了MM中肿瘤抗原异质性的概念,CAR-T细胞治疗的后果以及克服它的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overcoming tumor antigen heterogeneity in CAR-T cell therapy for malignant mesothelioma (MM)
Malignant mesothelioma (MM) is a rare, aggressive solid tumor with limited therapeutic options and poor therapeutic response. The role of immunotherapy in MM is now well established and therapeutic options, such as checkpoint inhibitors, are increasingly being approved. Chimeric antigen receptor (CAR)-T cell therapy is successfully implemented in several hematologic cancers, but currently has inadequate effect in solid tumors, owing to several limitations, such as trafficking and infiltration, limited T cell persistence and exhaustion, the immunosuppressive TME and tumor antigen heterogeneity. The lack of uniform and universal expression of tumor-associated antigens (TAAs) on tumor cells, as well as TAA heterogeneity following tumor editing post-therapy, are issues of significant importance to CAR-T cell and associated antigen-targeting therapies. Our review discusses the concept of tumor antigen heterogeneity in MM, the consequences for CAR-T cell therapies and the strategies to overcome it.
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来源期刊
CiteScore
3.20
自引率
5.30%
发文量
460
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