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设计细胞疗法用于组织再生

英文原题:Designer cell therapy for tissue regeneration.

查看英文原题

Designer cell therapy for tissue regeneration.

PubMed 2024/03/15(内容时间) Inflamm Regen Q1 · IF 7.7(JCR 2025)

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中文摘要

癌细胞治疗,特别是针对血液癌症的嵌合抗原受体(CAR)T细胞疗法,已成为一种强大的癌症治疗新模式。治疗性细胞与小分子和生物制剂等传统药物有显著不同,因为它们具备细胞信息处理能力,能够识别并响应体内的异常。这一能力使得治疗因子能够在特定位置和时间靶向递送。为克服CAR-T 细胞的不足并拓展其在实体瘤治疗中的功能,已开发并测试了多种工程化细胞。特别是,合成受体技术是设计能够特异性改善肿瘤微环境的治疗性细胞的关键。此类技术在再生受损组织方面也展现出巨大的医学应用潜力,而这些组织往往难以用传统药物治疗。在本综述中,我们介绍用于癌症治疗的新一代治疗性细胞的最新进展,并讨论工程化治疗性细胞在组织再生中的应用。

展开英文摘要原文

Cancer cell therapy, particularly chimeric antigen receptor (CAR) T-cell therapy for blood cancers, has emerged as a powerful new modality for cancer treatment. Therapeutic cells differ significantly from conventional drugs, such as small molecules and biologics, as they possess cellular information processing abilities to recognize and respond to abnormalities in the body. This capability enables the targeted delivery of therapeutic factors to specific locations and times. Various types of designer cells have been developed and tested to overcome the shortcomings of CAR T cells and expand their functions in the treatment of solid tumors.

In particular, synthetic receptor technologies are a key to designing therapeutic cells that specifically improve tumor microenvironment. Such technologies demonstrate great potential for medical applications to regenerate damaged tissues as well that are difficult to cure with conventional drugs. In this review, we introduce recent developments in next-generation therapeutic cells for cancer treatment and discuss the application of designer therapeutic cells for tissue regeneration.

论文信息

作者
Zama N、Toda S
第一作者单位
WPI Nano Life Science Institute (WPI-NanoLSI), Kanazawa University, Kakuma-machi, Kanazawa , 920-1192, Japan.Japan
通讯作者单位
WPI Nano Life Science Institute (WPI-NanoLSI), Kanazawa University, Kakuma-machi, Kanazawa , 920-1192, Japan. satoshi.toda@staff.kanazawa-u.ac.jp.Japan
文献类型
综述
期刊
Inflammation and regeneration2024 Mar 15
原文标识
PubMed 38491394 · DOI 10.1186/s41232-024-00327-4