In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles

التفاصيل البيبلوغرافية
العنوان: In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles
المؤلفون: Xiang Zhao, Qiang Liu, Hao Wan, Weizhi Wang, Shoujun Zhu, Ye Tian, Hongjie Dai, Jiachen Li, Yulai Liu, Feifei Wang, Zhuoran Ma, Yijun Yang, Mingxi Zhang, Yeteng Zhong, Haotian Du, Xi Wang, Qinchao Sun, Qiuhong Cui, K. Christopher Garcia
المصدر: Nature biotechnology
سنة النشر: 2019
مصطلحات موضوعية: Infrared Rays, medicine.medical_treatment, Dynamic imaging, CD8 Antigens, Biomedical Engineering, Nanoparticle, Bioengineering, Applied Microbiology and Biotechnology, B7-H1 Antigen, Article, 03 medical and health sciences, Mice, 0302 clinical medicine, Antineoplastic Agents, Immunological, Cancer immunotherapy, In vivo, Cell Line, Tumor, Quantum Dots, medicine, Tumor Microenvironment, Animals, 030304 developmental biology, 0303 health sciences, Chemistry, Optical Imaging, Immunotherapy, Xenograft Model Antitumor Assays, Colonic Neoplasms, Biophysics, Molecular Medicine, Nanoparticles, Molecular imaging, Luminescence, 030217 neurology & neurosurgery, Preclinical imaging, Biotechnology, Erbium, T-Lymphocytes, Cytotoxic
الوصف: 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. Biocompatible rare-earth nanoparticles with an emission maximum at 1,600 nm enable sensitive in vivo imaging.
تدمد: 1546-1696
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be34a6d4f6456743a04ed776bb911414
https://pubmed.ncbi.nlm.nih.gov/31570897
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....be34a6d4f6456743a04ed776bb911414
قاعدة البيانات: OpenAIRE