Author
Listed:
- Carlos E. Ruiz-Gonzalez
(Johns Hopkins University School of Medicine
Johns Hopkins University School of Medicine)
- Oscar J. Nino-Meza
(Johns Hopkins University School of Medicine
Johns Hopkins University School of Medicine)
- Medha Singh
(Johns Hopkins University School of Medicine
Johns Hopkins University School of Medicine)
- Yuderleys Masias-Leon
(Johns Hopkins University School of Medicine
Johns Hopkins University School of Medicine)
- Amy Kronenberg
(Johns Hopkins University School of Medicine)
- Madelynn Shambles
(Johns Hopkins University School of Medicine)
- Xueyi Chen
(Johns Hopkins University School of Medicine
Johns Hopkins University School of Medicine)
- Elizabeth W. Tucker
(Johns Hopkins University School of Medicine
Johns Hopkins University School of Medicine)
- Martin A. Lodge
(Johns Hopkins University School of Medicine)
- Laurence S. Carroll
(Johns Hopkins University School of Medicine)
- Kenneth R. Cooke
(Johns Hopkins University School of Medicine)
- Olivia S. Kates
(Johns Hopkins University School of Medicine)
- Shmuel Shoham
(Johns Hopkins University School of Medicine)
- Sean X. Zhang
(Johns Hopkins University School of Medicine)
- Sanjay K. Jain
(Johns Hopkins University School of Medicine
Johns Hopkins University School of Medicine
Johns Hopkins University School of Medicine)
Abstract
Invasive mold infections are a major cause of mortality in immunosuppressed and cancer patients. Diagnosis is challenging, requiring invasive procedures or reliance on fungal biomarkers with limited sensitivity and an inability to detect non-Aspergillus molds. Here, we perform whole-body 18F-fluorodeoxysorbitol (18F-FDS) positron emission tomography (PET) in nine prospectively enrolled patients with high-suspicion of invasive mold infections (eventually confirmed using culture or molecular assays, n = 4) or other pathologies (n = 5) with localization of 18F-FDS PET signal to infection sites as the primary outcome (NCT05611892). 18F-FDS PET (120 or 180 min after injection), rapidly detects and localizes invasive pulmonary and cerebral infections due to Aspergillus, non-Aspergillus (galactomannan-negative), or azole-resistant molds, and differentiates them from sterile inflammation or cancer. Moreover, 18F-FDS selectively and rapidly accumulates intracellularly in a range of clinically relevant molds, including azole-resistant molds, via a saturable process. In animals, 18F-FDS PET is able to detect and localize pulmonary and cerebral aspergillosis, as well as rhinosinusal infections due to Aspergillus, Rhizopus, and Mucor, confirming the clinical data. 18F-FDS can be easily synthesized from 18F-fluorodeoxyglucose (18F-FDG), which is widely available, and represents a promising, noninvasive diagnostic tool for detecting, localizing and monitoring of invasive mold infections throughout the body.
Suggested Citation
Carlos E. Ruiz-Gonzalez & Oscar J. Nino-Meza & Medha Singh & Yuderleys Masias-Leon & Amy Kronenberg & Madelynn Shambles & Xueyi Chen & Elizabeth W. Tucker & Martin A. Lodge & Laurence S. Carroll & Ken, 2025.
"18F-Fluorodeoxysorbitol PET for noninvasive detection of invasive mold infections: preclinical and first-in-human studies,"
Nature Communications, Nature, vol. 16(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-61700-6
DOI: 10.1038/s41467-025-61700-6
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