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18F-FDG PET Visualizes Systemic STING Agonist-Induced Lymphocyte Activation in Preclinical Models

Authors
 Thuc M Le  ;  Hailey R Lee  ;  Evan R Abt  ;  Khalid Rashid  ;  Amanda L Creech  ;  Keke Liang  ;  Jing Cui  ;  Arthur Cho  ;  Liu Wei  ;  Amanda Labora  ;  Charlotte Chan  ;  Eric Sanchez  ;  Kriti Kriti  ;  Daniel Karin  ;  Luyi Li  ;  Nanping Wu  ;  Christine Mona  ;  Giuseppe Carlucci  ;  Willy Hugo  ;  Ting-Ting Wu  ;  Timothy R Donahue  ;  Johannes Czernin  ;  Caius G Radu 
Citation
 JOURNAL OF NUCLEAR MEDICINE, Vol.64(1) : 117-123, 2023-01 
Journal Title
JOURNAL OF NUCLEAR MEDICINE
ISSN
 0161-5505 
Issue Date
2023-01
MeSH
Animals ; Fluorodeoxyglucose F18* / metabolism ; Lymphocyte Activation* ; Male ; Mice ; Mice, Inbred C57BL ; Positron-Emission Tomography ; Signal Transduction
Keywords
18F-FDG PET ; STING agonists ; immune activation ; immunometabolism ; lymphocytes
Abstract
Stimulator of interferon genes (STING) is a mediator of immune recognition of cytosolic DNA, which plays important roles in cancer, cytotoxic therapies, and infections with certain pathogens. Although pharmacologic STING activation stimulates potent antitumor immune responses in animal models, clinically applicable pharmacodynamic biomarkers that inform of the magnitude, duration, and location of immune activation elicited by systemic STING agonists are yet to be described. We investigated whether systemic STING activation induces metabolic alterations in immune cells that can be visualized by PET imaging.

Methods: C57BL/6 mice were treated with systemic STING agonists and imaged with 18F-FDG PET after 24 h. Splenocytes were harvested 6 h after STING agonist administration and analyzed by single-cell RNA sequencing and flow cytometry. 18F-FDG uptake in total splenocytes and immunomagnetically enriched splenic B and T lymphocytes from STING agonist-treated mice was measured by γ-counting. In mice bearing prostate or pancreas cancer tumors, the effects of STING agonist treatment on 18F-FDG uptake, T-lymphocyte activation marker levels, and tumor growth were evaluated.

Results: Systemic delivery of structurally distinct STING agonists in mice significantly increased 18F-FDG uptake in the spleen. The average spleen SUVmax in control mice was 1.90 (range, 1.56-2.34), compared with 4.55 (range, 3.35-6.20) in STING agonist-treated mice (P < 0.0001). Single-cell transcriptional and flow cytometry analyses of immune cells from systemic STING agonist-treated mice revealed enrichment of a glycolytic transcriptional signature in both T and B lymphocytes that correlated with the induction of immune cell activation markers. In tumor-bearing mice, STING agonist administration significantly delayed tumor growth and increased 18F-FDG uptake in secondary lymphoid organs.

Conclusion: These findings reveal hitherto unknown functional links between STING signaling and immunometabolism and suggest that 18F-FDG PET may provide a widely applicable approach toward measuring the pharmacodynamic effects of systemic STING agonists at a whole-body level and guiding their clinical development.
Files in This Item:
T202303540.pdf Download
DOI
10.2967/jnumed.122.264121
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Nuclear Medicine (핵의학교실) > 1. Journal Papers
Yonsei Authors
Cho, Arthur Eung Hyuck(조응혁) ORCID logo https://orcid.org/0000-0001-8670-2473
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/196414
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