← 返回

3D 生物打印免疫调节——下一代免疫肿瘤学的进展图景

英文原题:3D Bioprinted Immunomodulation─The Advancing Landscape of Next-Generation Immuno-oncology.

查看英文原题

3D Bioprinted Immunomodulation─The Advancing Landscape of Next-Generation Immuno-oncology.

PubMed 2025/05/30(内容时间) Biomacromolecules Q1 · IF 5.9(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

肿瘤微环境(TME)的改变可导致肿瘤发生,使肿瘤逃避免疫系统并扩散。因此,TME内的免疫调节可能是一种有用的治疗策略。在这方面,生物打印已成为开发治疗方案的潜在技术,这些方案提供了对免疫调节更好的控制。通过使用新型免疫细胞疗法和逼真的肿瘤模型,它为推进癌症免疫治疗提供了一个平台。通过研究肿瘤发生中免疫调节的复杂机制,这篇综述文章阐明了免疫系统与肿瘤微环境之间的相互作用如何影响癌症的发生和扩散。此外,还分析了3D生物打印在调节和激活免疫细胞(如T细胞、树突状细胞和巨噬细胞)方面的有效性。对当前研究的总结表明,3D生物打印在为推进抗癌研究和通过免疫治疗策略革新癌症治疗奠定坚实基础方面发挥着关键作用。

展开英文摘要原文

Tumor microenvironment (TME) alteration can lead to tumorigenesis, where tumors evade the immune system and spread.

Thus, immunomodulation inside the TME may be a useful therapeutic approach. In this regard, bioprinting has become a potential technique for developing therapeutic solutions that offer improved control over immune modulation.

Through the use of novel immune cell therapies and realistic tumor models, it provides a platform for advancing cancer immunotherapy. By examining the complex mechanisms of immunomodulation in tumorigenesis, this review article clarifies how interactions between the immune system and the tumor microenvironment affect the initiation and spread of cancer.

Additionally, the effectiveness of 3D bioprinting in modulating and activating immune cells, such as T cells, dendritic cells, and macrophages, has also been analyzed. A summary of current research shows the pivotal role of 3D bioprinting in establishing a solid foundation for advancing anticancer studies and revolutionizing cancer treatment through immunotherapeutic strategies.

论文信息

作者
Debnath S、Latiyan S、Jain N、Datta S、Pathote D、Bhowmick T、Mukherjee A
第一作者单位
Department of Materials Engineering, Indian Institute of Science, Bangalore 560012, India.India
通讯作者单位
Department of Zoology, Charuchandra College, University of Calcutta, Kolkata 700029, India.India
文献类型
综述
期刊
Biomacromolecules2025 Jun 9
原文标识
PubMed 40444674 · DOI 10.1021/acs.biomac.4c01816