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Updated: May 21, 2026

Analysis of 18FDG PET/CT Imaging as a Tool for Studying Mycobacterium tuberculosis Infection and Treatment in Non-human Primates
Published on: September 5, 2017
Infection dynamics and response to chemotherapy in a rabbit model of tuberculosis using [¹⁸F]2-fluoro-deoxy-D-glucose
Laura E Via1, Dan Schimel, Danielle M Weiner
1Tuberculosis Research Section, Laboratory of Clinical Infectious Diseases, National Institute for Allergy and Infectious Disease, National Institutes of Health, Bethesda, Maryland, USA.
Abstract:
With a host of new antitubercular chemotherapeutics in development, methods to assess the activity of these agents beyond mouse efficacy are needed to prioritize combinations for clinical trials. Lesions in Mycobacterium tuberculosis-infected rabbits are hypoxic, with histopathologic features that closely resemble those of human tuberculous lesions. Using [(18)F]2-fluoro-deoxy-d-glucose ([(18)F]FDG) positron emission tomography-computed tomography (PET-CT) imaging, we studied the dynamics of tuberculosis infection in rabbits, revealing an initial inflammatory response followed by a consolidative chronic disease. Five weeks after infection, as much as 23% of total lung volume was abnormal, but this was contained and to some extent reversed naturally by 9 weeks. During development of this chronic state, individual lesions in the same animal had very different fates, ranging from complete resolution to significant progression. Lesions that remained through the initial stage showed an increase in volume and tissue density over time by CT. Initiation of chemotherapy using either isoniazid (INH) or rifampin (RIF) during chronic infection reduced bacterial load with quantitative changes in [(18)F]FDG uptake, lesion density and total lesion volume measured by CT. The [(18)F]FDG PET uptake in lesions was significantly reduced with as little as 1 week of treatment, while the volume and density of lesions changed more slowly. The results from this study suggest that rabbits may be a useful surrogate species for evaluating novel chemotherapies and understanding changes in both PET and CT scans in human clinical trials.
Insights
New rabbit models show potential for testing tuberculosis drugs. Positron emission tomography-computed tomography (PET-CT) imaging reveals how lesions change, aiding the development of new antitubercular chemotherapeutics.
Area of Science:
- Infectious Diseases
- Medical Imaging
- Pharmacology
Background:
- Tuberculosis drug development requires better efficacy assessment methods beyond mouse models.
- Rabbit tuberculosis lesions share histopathologic similarities with human lesions, including hypoxia.
Purpose of the Study:
- To evaluate the utility of PET-CT imaging in studying tuberculosis infection dynamics in rabbits.
- To assess the rabbit as a surrogate model for testing novel antitubercular chemotherapeutics.
Main Methods:
- Utilized [(18)F]2-fluoro-deoxy-d-glucose ([(18)F]FDG) PET-CT imaging to monitor tuberculosis infection in rabbits.
- Observed lesion progression and resolution over time, and response to isoniazid (INH) and rifampin (RIF) chemotherapy.
Main Results:
- PET-CT revealed initial inflammation followed by chronic disease with variable lesion fates.
- Chemotherapy with INH or RIF reduced bacterial load and altered [(18)F]FDG uptake, lesion density, and volume.
- [(18)F]FDG uptake decreased rapidly within 1 week of treatment, while lesion volume and density changed more slowly.
Conclusions:
- Rabbits serve as a valuable surrogate species for evaluating novel tuberculosis chemotherapeutics.
- PET-CT imaging effectively captures dynamic changes in tuberculosis lesions during infection and treatment in rabbits.
- This model aids in understanding PET and CT scan changes relevant to human clinical trials.

