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.
Authors
- Martin A. Lodge (ORCID: https://orcid.org/0000-0003-0922-6519)
- Sanjay K. Jain (ORCID: https://orcid.org/0000-0001-9620-7070)
- Elizabeth W. Tucker (ORCID: https://orcid.org/0000-0002-0971-3635)
- Noah Lechtzin (ORCID: https://orcid.org/0000-0002-9088-8749)
- Nicole Parrish (ORCID: https://orcid.org/0000-0002-4263-228X)
- Joel S. Freundlich (ORCID: https://orcid.org/0000-0002-3411-3455)
- Xueyi Chen (ORCID: https://orcid.org/0000-0003-1574-7759)
- Kelly Flavahan
- Mona O. Sarhan (ORCID: https://orcid.org/0000-0002-0417-058X)
- Laurence S. Carroll (ORCID: https://orcid.org/0000-0001-8164-9474)
- Oscar J Nino-Meza
- Amy Kronenberg
- Medha Singh
- Carlos E Ruiz-Gonzalez
- Yuderleys Masias-Leon
Institutions
- Rutgers, The State University of New Jersey (US)
- Johns Hopkins University (US)
- Johns Hopkins Medicine (US)
- Johns Hopkins Hospital (US)
Publication Details
- 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