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

Yeteng Zhong, Zhuoran Ma, Feifei Wang, Xi Wang, Yijun Yang, Yulai Liu, Xiang Zhao, Jiachen Li, Haotian Du, Mingxi Zhang, Qiuhong Cui, Shoujun Zhu, Qinchao Sun, Hao Wan, Ye Tian, Qiang Liu, Weizhi Wang, K. Christopher Garcia, Hongjie Dai*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

438 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)1322-1331
Number of pages10
JournalNature Biotechnology
Volume37
Issue number11
DOIs
Publication statusPublished - 1 Nov 2019
Externally publishedYes

Fingerprint

Dive into the research topics of 'In vivo molecular imaging for immunotherapy using ultra-bright near-infrared-IIb rare-earth nanoparticles'. Together they form a unique fingerprint.

Cite this