File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1038/s41587-019-0262-4
- Scopus: eid_2-s2.0-85073967379
- PMID: 31570897
- WOS: WOS:000494984400020
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: 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 |
---|---|
Authors | |
Issue Date | 2019 |
Citation | Nature Biotechnology, 2019, v. 37, n. 11, p. 1322-1331 How to Cite? |
Abstract | 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. |
Persistent Identifier | http://hdl.handle.net/10722/325449 |
ISSN | 2023 Impact Factor: 33.1 2023 SCImago Journal Rankings: 18.117 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhong, Yeteng | - |
dc.contributor.author | Ma, Zhuoran | - |
dc.contributor.author | Wang, Feifei | - |
dc.contributor.author | Wang, Xi | - |
dc.contributor.author | Yang, Yijun | - |
dc.contributor.author | Liu, Yulai | - |
dc.contributor.author | Zhao, Xiang | - |
dc.contributor.author | Li, Jiachen | - |
dc.contributor.author | Du, Haotian | - |
dc.contributor.author | Zhang, Mingxi | - |
dc.contributor.author | Cui, Qiuhong | - |
dc.contributor.author | Zhu, Shoujun | - |
dc.contributor.author | Sun, Qinchao | - |
dc.contributor.author | Wan, Hao | - |
dc.contributor.author | Tian, Ye | - |
dc.contributor.author | Liu, Qiang | - |
dc.contributor.author | Wang, Weizhi | - |
dc.contributor.author | Garcia, K. Christopher | - |
dc.contributor.author | Dai, Hongjie | - |
dc.date.accessioned | 2023-02-27T07:33:25Z | - |
dc.date.available | 2023-02-27T07:33:25Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Nature Biotechnology, 2019, v. 37, n. 11, p. 1322-1331 | - |
dc.identifier.issn | 1087-0156 | - |
dc.identifier.uri | http://hdl.handle.net/10722/325449 | - |
dc.description.abstract | 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. | - |
dc.language | eng | - |
dc.relation.ispartof | Nature Biotechnology | - |
dc.title | In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1038/s41587-019-0262-4 | - |
dc.identifier.pmid | 31570897 | - |
dc.identifier.scopus | eid_2-s2.0-85073967379 | - |
dc.identifier.volume | 37 | - |
dc.identifier.issue | 11 | - |
dc.identifier.spage | 1322 | - |
dc.identifier.epage | 1331 | - |
dc.identifier.eissn | 1546-1696 | - |
dc.identifier.isi | WOS:000494984400020 | - |