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膜结合多模态等离激元换能器用于无创、原位监测与调控抗异质性实体瘤的 CAR-T 细胞

英文原题:Membrane-Bound Multimodal Plasmonic Transducers for Noninvasive, In Situ Monitoring and Control of CAR T Cells Against Heterogeneous Solid Tumors.

PubMed 2026/08/19(内容时间) Adv Mater Q1 · IF 29.1(JCR 2025)

研究概要

这些换能器在超过 20 mJ cm -2 的激光通量下表现出约 90% 的吸收效率和光稳定性,在多个激光循环中提供光声和热响应。

中文摘要

针对异质性实体瘤的 CAR T 细胞的无创监测与控制,仍是理解和改善治疗应答方面的主要挑战。为解决这一问题,开发了膜结合型等离激元换能器,其由各向异性框架中等离激元耦合的金纳米球组成,用于多模态光声成像以及 CAR T 细胞活性的局部热调控。这些换能器在超过 20 mJ cm -2 的激光能量密度下表现出约 90% 的吸收效率和光稳定性,可在多个激光循环中提供光声和热响应。因此,CAR T 细胞上的膜结合型换能器能够在激光激发下实现光声与热响应,而不损害关键细胞功能。在异质性 HER2 表达的乳腺肿瘤模型中,纵向光声成像能够基于早期 T 细胞转运对肿瘤进行前瞻性分层,以高灵敏度和高特异性预测应答者与无应答者。此外,换能器介导的对瘤内 CAR T 细胞的热调控——这些 CAR T 细胞经工程化改造、携带可分泌 T 细胞衔接器的热遗传回路——将细胞毒性重定向至抗原阴性肿瘤,克服了抗原逃逸,从而增强了治疗。综上所述,我们展示了一种通过膜结合型多模态换能器无创监测和控制 CAR T 细胞以对抗异质性实体瘤的策略。

展开英文摘要原文

Noninvasive monitoring and control of CAR T cells against heterogeneous solid tumors remain major challenges in understanding and improving treatment response. To address this, membrane-bound plasmonic transducers, composed of plasmonically coupled gold nanospheres in an anisotropic framework, were developed for multimodal photoacoustic imaging and localized thermal modulation of CAR T cell activity. These transducers exhibit approximately 90% absorption efficiency and photostability under laser fluences exceeding 20 mJ cm -2 , delivering photoacoustic and thermal responses over multiple lasing cycles. Membrane-bound transducers on CAR T cells thus enable photoacoustic and thermal responsiveness upon laser excitation without compromising key cellular functions. In heterogeneous HER2-expressing breast tumor models, longitudinal photoacoustic imaging enabled prospective stratification of tumors based on early T cell trafficking, predicting responders versus nonresponders with high sensitivity and specificity. Moreover, transducer-mediated thermal modulation of intratumoral CAR T cells engineered with thermogenetic circuits to secrete T cell engagers redirected cytotoxicity toward antigen-negative tumors, overcoming antigen escape and consequently enhancing therapy. Taken together, we demonstrate a strategy to noninvasively monitor and control CAR T cells against heterogeneous solid tumors via membrane-bound multimodal transducers.

论文信息

作者
Kim M、Zamat A、Cadena M、Thiveaud C、Sen R、Lee J、Kulaksizoglu E、Oliver SA
单位
Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, Georgia, USA.United States
期刊
Advanced materials (Deerfield Beach, Fla.)2026 Aug 19
原文标识
PubMed 42615383 · DOI 10.1002/adma.74686