CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Heat-inducible CAR-T overcomes adverse mechanical tumor microenvironment in a 3D bioprinted glioblastoma model.
Heat-inducible CAR-T overcomes adverse mechanical tumor microenvironment in a 3D bioprinted glioblastoma model.
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。
胶质母细胞瘤(GBM)现有治疗疗效有限,是重大治疗挑战。嵌合抗原受体(CAR)T 细胞疗法具有潜力,但细胞外基质(ECM)形成的物理屏障削弱其治疗实体瘤(如 GBM)的效果。为解决传统二维细胞培养、动物模型和 Matrigel 三维培养难以模拟肿瘤组织力学特性的不足,本研究采用生物材料和基于数字光处理的三维生物打印技术,制造仿生肿瘤模型,可独立于 ECM 成分精确调节基质硬度。结果显示,材料硬度增加显著阻碍 CAR-T 细胞在 GBM 模型中的穿透和肿瘤细胞毒性。三维生物打印模型可用于研究 ECM 硬度对 CAR-T 疗效的影响,为在坚硬实体瘤中开发 CAR-T 提供具有临床相关性的评估工具。此外,研究开发了一种创新的热诱导 CAR-T 疗法,可有效克服坚硬肿瘤微环境的障碍。
Glioblastoma (GBM) presents a significant therapeutic challenge due to the limited efficacy of existing treatments. Chimeric antigen receptor (CAR) T-cell therapy offers promise, but its potential in solid tumors like GBM is undermined by the physical barrier posed by the extracellular matrix (ECM).
To address the inadequacies of traditional 2D cell culture, animal models, and Matrigel-based 3D culture in mimicking the mechanical characteristics of tumor tissues, we employed biomaterials and digital light processing-based 3D bioprinting to fabricate biomimetic tumor models with finely tunable ECM stiffness independent of ECM composition.
Our results demonstrated that increased material stiffness markedly impeded CAR-T cell penetration and tumor cell cytotoxicity in GBM models. The 3D bioprinted models enabled us to examine the influence of ECM stiffness on CAR-T cell therapy effectiveness, providing a clinically pertinent evaluation tool for CAR-T cell development in stiff solid tumors.
Furthermore, we developed an innovative heat-inducible CAR-T cell therapy, effectively overcoming the challenges posed by the stiff tumor microenvironment.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。