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CAR-T 细胞治疗:肺癌中的挑战与机遇

英文原题:Chimeric antigen receptor T-cell therapy: challenges and opportunities in lung cancer.

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Chimeric antigen receptor T-cell therapy: challenges and opportunities in lung cancer.

PubMed 2022/02/23(内容时间) Antib Ther Q2 · IF 4.8(JCR 2025)

研究概要

嵌合抗原受体(CAR)T细胞疗法已经彻底改变了血液系统恶性肿瘤治疗的范式,推动了越来越多的基础研究和临床试验,这些研究和试验旨在通过基因工程改造T细胞来治疗实体瘤。

中文摘要

嵌合抗原受体(CAR)T细胞疗法已经彻底改变了血液系统恶性肿瘤治疗的范式,推动了越来越多的基础研究和临床试验,这些研究和试验旨在通过基因工程改造T细胞来治疗实体瘤。基于靶向Mesothelin、CEA、EGFR、EGFR、MUC1、DLL3以及新兴新靶点的抗体的CAR T细胞疗法为肺癌患者提供了有希望的疗效。然而,由于物理和免疫屏障、抗原逃逸和异质性、靶向非肿瘤毒性以及许多其他原因,CAR T细胞疗法针对肺癌的临床应用仍然有限。了解CAR结构的演变、制造CAR T细胞的通用要求以及肺部肿瘤免疫学与CAR T细胞之间的相互作用,将改善这种治疗方式在肺癌中的临床转化。在这篇综述中,我们系统总结了CAR T细胞疗法在肺癌中的最新进展,重点关注CAR结构、靶抗原、挑战以及相应的新策略。

展开英文摘要原文

Chimeric antigen receptor (CAR) T-cell therapy has revolutionized the paradigm in hematological malignancies treatment, driving an ever-expanding number of basic research and clinical trials of genetically engineering T cells to treat solid tumors. CAR T-cell therapies based on the antibodies targeting Mesothelin, CEA, EGFR, EGFR, MUC1, DLL3, and emerging novel targets provide promising efficacy for lung cancer patients. However, clinical application of CAR T-cell therapy against lung cancer remains limited on account of physical and immune barriers, antigen escape and heterogeneity, on-target off-tumor toxicity, and many other reasons. Understanding the evolution of CAR structure and the generalizable requirements for manufacturing CAR T cells as well as the interplay between lung tumor immunology and CAR T cells will improve clinical translation of this therapeutic modality in lung cancer. In this review, we systematically summarize the latest advances in CAR T-cell therapy in lung cancer, focusing on the CAR structure, target antigens, challenges, and corresponding new strategies.

论文信息

作者
Xu C、Ju D、Zhang X
单位
Department of Biological Medicines & Shanghai Engineering Research Center of Immunotherapeutics, School of Pharmacy, Fudan University, Shanghai 201203, China.China
文献类型
综述
期刊
Antibody therapeutics2022 Jan
原文标识
PubMed 35372786 · DOI 10.1093/abt/tbac006