嵌合抗原受体
免疫疗法
翻译(生物学)
计算生物学
计算机科学
风险分析(工程)
纳米技术
钥匙(锁)
医学
肿瘤微环境
产品(数学)
生化工程
实体瘤
现成的
先天免疫系统
细胞疗法
免疫学
组分(热力学)
生物
临床实习
工程伦理学
边疆
工程类
肿瘤细胞
癌症研究
作者
Maram Alrehaili,Pedro Silva Couto,Rana Khalife,Qasim A. Rafiq
标识
DOI:10.1038/s41698-025-01170-7
摘要
Chimeric antigen receptor macrophages (CAR-Ms) represent a promising frontier in immunotherapy, leveraging both innate and engineered capabilities to combat solid tumors. CAR-Ms can actively remodel the tumor microenvironment while directly targeting tumor cells through CAR signaling, making them a potential alternative to existing cell-based therapies. Pre-clinical and clinical evidence suggests that CAR-M therapy holds significant promise for treating solid tumors. However, its clinical translation remains challenging due to restricted cell expansion, genetic engineering complexities, and variability in product quality. This article reviews recent advances in the CAR-M field, discussing the biological rationale behind this approach, key preclinical findings, and technological innovations necessary to facilitate clinical success as a versatile, off the shelf immunotherapy for hard-to-treat solid malignancies.
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