Analysis of 18FDG PET/CT Imaging as a Tool for Studying Mycobacterium tuberculosis Infection and Treatment in Non-human Primates.

Analysis of 18FDG PET/CT Imaging as a Tool for Studying Mycobacterium tuberculosis Infection and Treatment in Non-human Primates.
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DOI:
10.3791/56375
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发表时间:
2017-09
期刊:
Journal of visualized experiments : JoVE
影响因子:
--
通讯作者:
Alexander G. White;Pauline Maiello;M. Coleman;Jaime Tomko;L. Frye;C. Scanga;P. Lin;JoAnne L. Flynn
Alexander G. White;Pauline Maiello;M. Coleman;Jaime Tomko;L. Frye;C. Scanga;P. Lin;JoAnne L. Flynn
中科院分区:
其他
文献类型:
--
作者:
Alexander G. White;Pauline Maiello;M. Coleman;Jaime Tomko;L. Frye;C. Scanga;P. Lin;JoAnne L. Flynn

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Mycobacterium tuberculosis remains the number one infectious agent in the world today. With the emergence of antibiotic resistant strains, new clinically relevant methods are needed that evaluate the disease process and screen for potential antibiotic and vaccine treatments. Positron Emission Tomography/Computed Tomography (PET/CT) has been established as a valuable tool for studying a number of afflictions such as cancer, Alzheimer's disease, and inflammation/infection. Outlined here are a number of strategies that have been employed to evaluate PET/CT images in cynomolgus macaques that are infected intrabronchially with low doses of M. tuberculosis. Through evaluation of lesion size on CT and uptake of 18F-fluorodeoxyglucose (FDG) in lesions and lymph nodes in PET images, these described methods show that PET/CT imaging can predict future development of active versus latent disease and the propensity for reactivation from a latent state of infection. Additionally, by analyzing the overall level of lung inflammation, these methods determine antibiotic efficacy of drugs against M. tuberculosis in the most clinically relevant existing animal model. These image analysis methods are some of the most powerful tools in the arsenal against this disease as not only can they evaluate a number of characteristics of infection and drug treatment, but they are also directly translatable to a clinical setting for use in human studies.