Department of Chemistry and Bio-X, Stanford University, Stanford, CA, USA.
Key Laboratory of Luminescence and Optical Information, Ministry of Education, Department of Physics, School of Science, Beijing Jiaotong University, Beijing, China.
Nat Biotechnol. 2019 Nov;37(11):1322-1331. doi: 10.1038/s41587-019-0262-4. Epub 2019 Sep 30.
The near-infrared-IIb (NIR-IIb) (1,500-1,700 nm) window is ideal for deep-tissue optical imaging in mammals, but lacks bright and biocompatible probes. Here, we developed biocompatible cubic-phase (α-phase) erbium-based rare-earth nanoparticles (ErNPs) exhibiting bright downconversion luminescence at 1,600 nm for dynamic imaging of cancer immunotherapy in mice. We used ErNPs functionalized with cross-linked hydrophilic polymer layers attached to anti-PD-L1 (programmed cell death-1 ligand-1) antibody for molecular imaging of PD-L1 in a mouse model of colon cancer and achieved tumor-to-normal tissue signal ratios of ~40. The long luminescence lifetime of ErNPs (4.6 ms) enabled simultaneous imaging of ErNPs and lead sulfide quantum dots emitting in the same ~1,600 nm window. In vivo NIR-IIb molecular imaging of PD-L1 and CD8 revealed cytotoxic T lymphocytes in the tumor microenvironment in response to immunotherapy, and altered CD8 signals in tumor and spleen due to immune activation. The cross-linked functionalization layer facilitated 90% ErNP excretion within 2 weeks without detectable toxicity in mice.
近红外二区(NIR-IIb)(1500-1700nm)窗口非常适合哺乳动物的深层组织光学成像,但缺乏明亮且生物兼容的探针。在这里,我们开发了生物兼容的立方相(α相)铒基稀土纳米颗粒(ErNPs),在1600nm 处表现出明亮的下转换发光,用于在小鼠中进行癌症免疫治疗的动态成像。我们使用交联亲水性聚合物层修饰的 ErNPs,附着有抗 PD-L1(程序性死亡配体-1)抗体,用于在结直肠癌小鼠模型中进行 PD-L1 的分子成像,并实现了肿瘤与正常组织信号比约为 40。ErNPs 的长荧光寿命(4.6ms)使得能够同时对 ErNPs 和在相同~1600nm 窗口中发射的硫化铅量子点进行成像。体内 NIR-IIb 分子成像显示 PD-L1 和 CD8 揭示了肿瘤微环境中的细胞毒性 T 淋巴细胞对免疫治疗的反应,以及由于免疫激活导致肿瘤和脾脏中 CD8 信号的改变。交联功能化层促进了 90%的 ErNP 在 2 周内排出,而在小鼠中没有检测到毒性。