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嵌合抗原受体(CAR)细胞效应器的谱系:抗肿瘤免疫中的作用模式

The Spectrum of CAR Cellular Effectors: Modes of Action in Anti-Tumor Immunity.

作者信息

Nguyen Ngoc Thien Thu, Müller Rasmus, Briukhovetska Daria, Weber Justus, Feucht Judith, Künkele Annette, Hudecek Michael, Kobold Sebastian

机构信息

Division of Clinical Pharmacology, Department of Medicine IV, LMU University Hospital, LMU Munich, 80336 Munich, Germany.

German Cancer Consortium (DKTK), Partner Site Munich, a Partnership between the DKFZ Heidelberg and the University Hospital of the LMU, 80336 Munich, Germany.

出版信息

Cancers (Basel). 2024 Jul 22;16(14):2608. doi: 10.3390/cancers16142608.

Abstract

Chimeric antigen receptor-T cells have spearheaded the field of adoptive cell therapy and have shown remarkable results in treating hematological neoplasia. Because of the different biology of solid tumors compared to hematological tumors, response rates of CAR-T cells could not be transferred to solid entities yet. CAR engineering has added co-stimulatory domains, transgenic cytokines and switch receptors to improve performance and persistence in a hostile tumor microenvironment, but because of the inherent cell type limitations of CAR-T cells, including HLA incompatibility, toxicities (cytokine release syndrome, neurotoxicity) and high costs due to the logistically challenging preparation process for autologous cells, the use of alternative immune cells is gaining traction. NK cells and γδ T cells that do not need HLA compatibility or macrophages and dendritic cells with additional properties such as phagocytosis or antigen presentation are increasingly seen as cellular vehicles with potential for application. As these cells possess distinct properties, clinicians and researchers need a thorough understanding of their peculiarities and commonalities. This review will compare these different cell types and their specific modes of action seen upon CAR activation.

摘要

嵌合抗原受体T细胞引领了过继性细胞治疗领域,并在治疗血液系统肿瘤方面取得了显著成效。由于实体瘤与血液肿瘤的生物学特性不同,CAR-T细胞的应答率尚未能应用于实体瘤。CAR工程添加了共刺激结构域、转基因细胞因子和开关受体,以提高其在恶劣肿瘤微环境中的性能和持久性,但由于CAR-T细胞存在固有的细胞类型限制,包括HLA不相容性、毒性(细胞因子释放综合征、神经毒性)以及自体细胞制备过程中后勤保障困难导致的高成本,替代免疫细胞的应用越来越受到关注。不需要HLA相容性的NK细胞和γδT细胞,或具有吞噬作用或抗原呈递等额外特性的巨噬细胞和树突状细胞,越来越被视为具有应用潜力的细胞载体。由于这些细胞具有不同的特性,临床医生和研究人员需要深入了解它们的独特之处和共性。本综述将比较这些不同的细胞类型及其在CAR激活时的具体作用方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cccd/11274444/b0f164dd8d52/cancers-16-02608-g001.jpg

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