Department of Electrical & Computer Engineering, University of Toronto, Toronto, Ontario M5S3G4, Canada.
Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States.
ACS Nano. 2024 Aug 13;18(32):21554-21564. doi: 10.1021/acsnano.4c07306. Epub 2024 Jul 30.
While existing synthetic technologies for ex vivo T-cell activation face challenges like suboptimal expansion rates and low effectiveness, artificial antigen-presenting cells (aAPCs) hold great promise for enhanced T-cell based therapies. In particular, gold nanoparticles (AuNPs), known for their biocompatibility, ease of synthesis, and versatile surface chemistry, are strong candidates for use as nanoscale aAPCs. In this study, we developed spiky AuNPs with branched geometries to present activating ligands to primary human T-cells. The special structure of spiky AuNPs enhances biomolecule loading capacity and significantly improves T-cell activation through multivalent binding of costimulatory ligands and receptors. Our spiky AuNPs outperform existing systems including Dynabeads and soluble activators by promoting greater polyclonal expansion of T-cells, boosting sustained cytokine production, and generating highly functional T-cells with reduced exhaustion. In addition, spiky AuNPs effectively activate and expand CD19 CAR-T cells while demonstrating increased in vitro cytotoxicity against target cells using fewer effector cells than Dynabeads. This study underscores the potential of spiky AuNPs as a powerful tool, bringing new opportunities to adoptive cell therapy applications.
虽然现有的体外 T 细胞激活的合成技术面临着一些挑战,如扩增率不理想和效果低下,但人工抗原呈递细胞(aAPC)在增强基于 T 细胞的治疗方面具有很大的潜力。特别是金纳米颗粒(AuNPs),由于其生物相容性、易于合成和多功能的表面化学性质,是作为纳米级 aAPC 的理想候选材料。在这项研究中,我们开发了具有分支结构的刺状 AuNPs,以向原代人 T 细胞呈递激活配体。刺状 AuNPs 的特殊结构增强了生物分子的负载能力,并通过共刺激配体和受体的多价结合显著提高了 T 细胞的激活。与现有的系统,包括 Dynabeads 和可溶性激活剂相比,我们的刺状 AuNPs 能够促进 T 细胞的多克隆扩增,提高细胞因子的持续产生,并产生具有低衰竭的高功能 T 细胞。此外,刺状 AuNPs 可以有效激活和扩增 CD19 CAR-T 细胞,同时与 Dynabeads 相比,使用更少的效应细胞对靶细胞表现出增强的体外细胞毒性。这项研究强调了刺状 AuNPs 作为一种强大工具的潜力,为过继细胞治疗应用带来了新的机遇。