Dynamic 11C– <i>Para</i> –Aminobenzoic Acid Positron Emission Tomography/Computed Tomography for Visualizing Pulmonary <i>Mycobacteroides abscessus</i> Infections

<b>Rationale:</b> <i>Mycobacteroides abscessus</i> infections affect immunocompromised patients and those with underlying pulmonary disease. Conventional imaging cannot distinguish <i>M. abscessus</i> infections from underlying pulmonary disease or sterile inflammation, requiring invasive procedures for definitive diagnosis. <b>Objectives:</b> We evaluated <sup>11</sup>C-<i>para</i>-aminobenzoic acid (<sup>11</sup>C-PABA), a chemically identical radioanalog of PABA, to detect and localize infections due to <i>M. abscessus</i>. <b>Methods:</b> <i>In vitro</i> uptake assays were performed to test the metabolism and accumulation of PABA into <i>M. abscessus</i> reference and clinical isolates. Dynamic <sup>11</sup>C-PABA positron emission tomography (PET) was performed in a mouse model of <i>M. abscessus</i> pulmonary infection and in a patient with microbiologically confirmed <i>M. abscessus</i> pulmonary infection (NCT05611905). <b>Measurements and Main Results:</b> <sup>11</sup>C-PABA was intracellularly metabolized by <i>M. abscessus</i> to <sup>11</sup>C-7,8-dihydropteroate. In addition, the reference strain and all 13 randomly chosen clinical isolates, including 3 resistant to trimethoprim-sulfamethoxazole, rapidly accumulated PABA. No PABA accumulation was noted by heat-inactivated bacteria or mammalian cells. Dynamic <sup>11</sup>C-PABA PET in a mouse model of <i>M. abscessus</i> pulmonary infection rapidly distinguished infection from sterile inflammation and also accurately monitored response to antibiotic treatment. Finally, dynamic <sup>11</sup>C-PABA PET in a 33-year-old woman with cystic fibrosis and microbiologically confirmed <i>M. abscessus</i> pulmonary infection was safe and demonstrated significantly higher and sustained PET uptake in the affected lesions. <b>Conclusions:</b> <sup>11</sup>C-PABA PET is an innovative, clinically translatable, noninvasive, bacteria-specific diagnostic to differentiate <i>M. abscessus</i> infections from underlying pulmonary disease in patients. This tool could also help in monitoring treatment responses and enable precision medicine approaches for patients with complicated infections.

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Journal
American Journal of Respiratory and Critical Care Medicine
Published
2025-03-28
DOI
https://doi.org/10.1164/rccm.202409-1792oc
Citations
2
Primary Topic
Mycobacterium research and diagnosis
Type
article
Field-Weighted Citation Impact
2.71
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article

Dynamic 11C– Para –Aminobenzoic Acid Positron Emission Tomography/Computed Tomography for Visualizing Pulmonary Mycobacteroides abscessus Infections

Martin A. Lodge, Sanjay K. Jain, Elizabeth W. Tucker, Noah Lechtzin et al.
2 citations
American Journal of Respiratory and Critical Care Medicine
Mycobacterium research and diagnosis
2.71
article

Dynamic 11C– Para –Aminobenzoic Acid Positron Emission Tomography/Computed Tomography for Visualizing Pulmonary Mycobacteroides abscessus Infections

Martin A. Lodge, Sanjay K. Jain, Elizabeth W. Tucker, Noah Lechtzin, Nicole Parrish, Joel S. Freundlich, Xueyi Chen, Kelly Flavahan, Mona O. Sarhan, Laurence S. Carroll, Oscar J Nino-Meza, Amy Kronenberg, Medha Singh, Carlos E Ruiz-Gonzalez, Yuderleys Masias-Leon
article en
2 citations

Abstract

<b>Rationale:</b> <i>Mycobacteroides abscessus</i> infections affect immunocompromised patients and those with underlying pulmonary disease. Conventional imaging cannot distinguish <i>M. abscessus</i> infections from underlying pulmonary disease or sterile inflammation, requiring invasive procedures for definitive diagnosis. <b>Objectives:</b> We evaluated <sup>11</sup>C-<i>para</i>-aminobenzoic acid (<sup>11</sup>C-PABA), a chemically identical radioanalog of PABA, to detect and localize infections due to <i>M. abscessus</i>. <b>Methods:</b> <i>In vitro</i> uptake assays were performed to test the metabolism and accumulation of PABA into <i>M. abscessus</i> reference and clinical isolates. Dynamic <sup>11</sup>C-PABA positron emission tomography (PET) was performed in a mouse model of <i>M. abscessus</i> pulmonary infection and in a patient with microbiologically confirmed <i>M. abscessus</i> pulmonary infection (NCT05611905). <b>Measurements and Main Results:</b> <sup>11</sup>C-PABA was intracellularly metabolized by <i>M. abscessus</i> to <sup>11</sup>C-7,8-dihydropteroate. In addition, the reference strain and all 13 randomly chosen clinical isolates, including 3 resistant to trimethoprim-sulfamethoxazole, rapidly accumulated PABA. No PABA accumulation was noted by heat-inactivated bacteria or mammalian cells. Dynamic <sup>11</sup>C-PABA PET in a mouse model of <i>M. abscessus</i> pulmonary infection rapidly distinguished infection from sterile inflammation and also accurately monitored response to antibiotic treatment. Finally, dynamic <sup>11</sup>C-PABA PET in a 33-year-old woman with cystic fibrosis and microbiologically confirmed <i>M. abscessus</i> pulmonary infection was safe and demonstrated significantly higher and sustained PET uptake in the affected lesions. <b>Conclusions:</b> <sup>11</sup>C-PABA PET is an innovative, clinically translatable, noninvasive, bacteria-specific diagnostic to differentiate <i>M. abscessus</i> infections from underlying pulmonary disease in patients. This tool could also help in monitoring treatment responses and enable precision medicine approaches for patients with complicated infections.

American Journal of Respiratory and Critical Care MedicineVol. 211(7)
Rutgers, The State University of New Jersey (US), Johns Hopkins University (US), Johns Hopkins Medicine (US), Johns Hopkins Hospital (US)
Good health and well-being
Openalex Percentile: Top 11%
Mycobacterium research and diagnosis
2.71
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