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11C-Para-aminobenzoic acid PET imaging of S. aureus and MRSA infection in preclinical models and humans
Alvaro A. Ordonez, … , David M. Wilson, Sanjay K. Jain
Alvaro A. Ordonez, … , David M. Wilson, Sanjay K. Jain
Published January 11, 2022
Citation Information: JCI Insight. 2022;7(1):e154117. https://doi.org/10.1172/jci.insight.154117.
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Resource and Technical Advance Infectious disease

11C-Para-aminobenzoic acid PET imaging of S. aureus and MRSA infection in preclinical models and humans

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Abstract

Tools for noninvasive detection of bacterial pathogens are needed but are not currently available for clinical use. We have previously shown that para-aminobenzoic acid (PABA) rapidly accumulates in a wide range of pathogenic bacteria, motivating the development of related PET radiotracers. In this study, 11C-PABA PET imaging was used to accurately detect and monitor infections due to pyogenic bacteria in multiple clinically relevant animal models. 11C-PABA PET imaging selectively detected infections in muscle, intervertebral discs, and methicillin-resistant Staphylococcus aureus–infected orthopedic implants. In what we believe to be first-in-human studies in healthy participants, 11C-PABA was safe, well-tolerated, and had a favorable biodistribution, with low background activity in the lungs, muscles, and brain. 11C-PABA has the potential for clinical translation to detect and localize a broad range of bacteria.

Authors

Alvaro A. Ordonez, Matthew F.L. Parker, Robert J. Miller, Donika Plyku, Camilo A. Ruiz-Bedoya, Elizabeth W. Tucker, Justin M. Luu, Dustin A. Dikeman, Wojciech G. Lesniak, Daniel P. Holt, Robert F. Dannals, Lloyd S. Miller, Steven P. Rowe, David M. Wilson, Sanjay K. Jain

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Figure 2

11C-PABA PET/CT imaging in a rabbit model of MRSA prosthetic joint infection.

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11C-PABA PET/CT imaging in a rabbit model of MRSA prosthetic joint infe...
(A) A prosthetic metal implant was inserted into the femur of Dutch Belted rabbits and subsequently infected with MRSA (n = 3). (B) Progression of the infection was observed by optical imaging. Seven days after infection, the bioluminescent bacteria were visible over the knee. (C) Maximum intensity projection (MIP) and sagittal and transverse views of 11C-PABA PET/CT images from a representative rabbit where the 11C-PABA signal can be seen at the site of infection (purple to yellow). Minimum background is observed in the contralateral unaffected muscle and bone. (D) Quantification of the 11C-PABA PET signal, represented as median ± IQR of infection vs. unaffected muscle target-to-nontarget ratio.

Copyright © 2022 American Society for Clinical Investigation
ISSN 2379-3708

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