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CAR-T 细胞纳米共生体:揭示新型二元组合的无限潜力

英文原题:CAR T Cell Nanosymbionts: Revealing the Boundless Potential of a New Dyad.

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CAR T Cell Nanosymbionts: Revealing the Boundless Potential of a New Dyad.

PubMed 2024/12/07(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

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中文摘要

传统癌症治疗主要聚焦清除肿瘤细胞,但面临耐药和毒性等挑战。利用CAR-T 细胞免疫疗法靶向肿瘤微环境是一种有前景的新方向;该疗法已显示治疗复发/难治性癌症的潜力,但受到成本高、耐药及毒性等限制,实体瘤中尤为如此。将纳米技术整合至细胞免疫疗法(ICAM),我们称为“CAR-T 纳米共生”,可带来克服这些挑战的新机会。纳米材料可改善CAR-T 细胞递送、制备、活性调节及肿瘤微环境靶向能力,实现更好的控制和精准度。该方法旨在提高CAR-T 细胞治疗实体瘤的效力、减少相关毒性并最终改善患者结局。多项研究已显示良好结果;进一步开发该疗法,对于提高其可及性和效力至关重要。我们的“加法即减法模型”将这些多方面因素整合为统一策略,以推进癌症治疗模式。

展开英文摘要原文

Cancer treatment has traditionally focused on eliminating tumor cells but faces challenges such as resistance and toxicity. A promising direction involves targeting the tumor microenvironment using CAR T cell immunotherapy, which has shown potential for treating relapsed and refractory cancers but is limited by high costs, resistance, and toxicity, especially in solid tumors. The integration of nanotechnology into ICAM cell therapy, a concept we have named "CAR T nanosymbiosis", offers new opportunities to overcome these challenges.

Nanomaterials can enhance CAR T cell delivery, manufacturing, activity modulation, and targeting of the tumor microenvironment, providing better control and precision. This approach aims to improve the efficacy of CAR T cells against solid tumors, reduce associated toxicities, and ultimately enhance patient outcomes. Several studies have shown promising results, and developing this therapy further is essential for increasing its accessibility and effectiveness.

Our "addition by subtraction model" synthesizes these multifaceted elements into a unified strategy to advance cancer treatment paradigms.

论文信息

作者
Baena JC、Pérez LM、Toro-Pedroza A、Kitawaki T、Loukanov A
第一作者单位
Division of Oncology, Department of Medicine, Fundación Valle del Lili, ICESI University, Carrera 98 No. 18-49, Cali 760032, Colombia.
通讯作者单位
Department of Chemistry and Materials Science, National Institute of Technology, Gunma College, Maebashi 371-8530, Japan.Japan
文献类型
综述
期刊
International journal of molecular sciences2024 Dec 7
原文标识
PubMed 39684867 · DOI 10.3390/ijms252313157