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In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles
The NIR-IIb (1500–1700 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 ~ 1600 nm for dynami...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858548/ https://www.ncbi.nlm.nih.gov/pubmed/31570897 http://dx.doi.org/10.1038/s41587-019-0262-4 |
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author | Zhong, Yeteng Ma, Zhuoran Wang, Feifei Wang, Xi Yang, Yijun Liu, Yulai Zhao, Xiang Li, Jiachen Du, Haotian Zhang, Mingxi Cui, Qiuhong Zhu, Shoujun Sun, Qinchao Wan, Hao Tian, Ye Liu, Qiang Wang, Weizhi Garcia, K. Christopher Dai, Hongjie |
author_facet | Zhong, Yeteng Ma, Zhuoran Wang, Feifei Wang, Xi Yang, Yijun Liu, Yulai Zhao, Xiang Li, Jiachen Du, Haotian Zhang, Mingxi Cui, Qiuhong Zhu, Shoujun Sun, Qinchao Wan, Hao Tian, Ye Liu, Qiang Wang, Weizhi Garcia, K. Christopher Dai, Hongjie |
author_sort | Zhong, Yeteng |
collection | PubMed |
description | The NIR-IIb (1500–1700 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 ~ 1600 nm for dynamic imaging of cancer immune-therapy in mice. We used ErNPs functionalized with cross-linked hydrophilic polymer layers attached to anti-PD-L1 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 (PbS QDs) emitting in the same ~ 1600 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 novel crosslinked functionalization layer facilitated 90% ErNPs excretion within two weeks without detectable toxicity in mice. |
format | Online Article Text |
id | pubmed-6858548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-68585482020-03-30 In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles Zhong, Yeteng Ma, Zhuoran Wang, Feifei Wang, Xi Yang, Yijun Liu, Yulai Zhao, Xiang Li, Jiachen Du, Haotian Zhang, Mingxi Cui, Qiuhong Zhu, Shoujun Sun, Qinchao Wan, Hao Tian, Ye Liu, Qiang Wang, Weizhi Garcia, K. Christopher Dai, Hongjie Nat Biotechnol Article The NIR-IIb (1500–1700 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 ~ 1600 nm for dynamic imaging of cancer immune-therapy in mice. We used ErNPs functionalized with cross-linked hydrophilic polymer layers attached to anti-PD-L1 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 (PbS QDs) emitting in the same ~ 1600 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 novel crosslinked functionalization layer facilitated 90% ErNPs excretion within two weeks without detectable toxicity in mice. 2019-09-30 2019-11 /pmc/articles/PMC6858548/ /pubmed/31570897 http://dx.doi.org/10.1038/s41587-019-0262-4 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Zhong, Yeteng Ma, Zhuoran Wang, Feifei Wang, Xi Yang, Yijun Liu, Yulai Zhao, Xiang Li, Jiachen Du, Haotian Zhang, Mingxi Cui, Qiuhong Zhu, Shoujun Sun, Qinchao Wan, Hao Tian, Ye Liu, Qiang Wang, Weizhi Garcia, K. Christopher Dai, Hongjie In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles |
title | In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles |
title_full | In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles |
title_fullStr | In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles |
title_full_unstemmed | In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles |
title_short | In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles |
title_sort | in vivo molecular imaging for immunotherapy using ultra-bright near-infrared-iib rare-earth nanoparticles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858548/ https://www.ncbi.nlm.nih.gov/pubmed/31570897 http://dx.doi.org/10.1038/s41587-019-0262-4 |
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