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Imaging of immunocompromised patients: focus on fungal-specific PET tracers
1Center for Infectious Disease Imaging (CIDI), Radiology and Imaging Sciences, Clinical Center (CC), National Institutes of Health (NIH), Maryland, MD, USA.
Abstract:
The global population of immunocompromised patients is growing, accompanied by a rising incidence of opportunistic infections. Among these, invasive mold infections are associated with substantial morbidity and mortality, in part because of delayed diagnosis. Although current diagnostic methods have improved, they are still limited by lack of specificity, invasiveness, or both. Recently, several novel noninvasive, pathogen-specific PET imaging ligands have been developed and evaluated. Among them, [18F]-fluorocellobiose, a carbohydrate-based metabolic tracer, has demonstrated high specificity for live cellulolytic mold infections, including Aspergillus spp. It also shows promise for treatment monitoring and can be readily synthesized enzymatically from [18F]-fluorodeoxyglucose. ImmunoPET approaches targeting fungal cell wall components are likewise highly promising as panfungal ligands and may be further optimized through antibody engineering strategies to enhance target binding, functionality and pharmacokinetic properties. These newer PET ligands have the potential to overcome the limited specificity of [18F]-FDG, allowing more accurate localization of infectious lesions and, importantly, differentiation between invasive fungal infections and other types of pathogens. Such advances are especially significant for this vulnerable patient population, in whom rapid and accurate diagnosis can have major prognostic implications.
Insights
Novel positron emission tomography (PET) imaging ligands offer improved, noninvasive detection of invasive mold infections in immunocompromised patients. These tracers enhance diagnostic accuracy, aiding timely treatment and improving patient prognoses.
Area of Science:
- Medical Imaging
- Infectious Diseases
- Nuclear Medicine
Background:
- Growing population of immunocompromised individuals leads to increased opportunistic infections.
- Invasive mold infections pose significant morbidity and mortality due to diagnostic challenges.
- Current diagnostic methods for invasive fungal infections lack specificity or are invasive.
Purpose of the Study:
- To review novel noninvasive positron emission tomography (PET) imaging ligands for diagnosing invasive mold infections.
- To highlight the potential of specific PET tracers in improving diagnostic accuracy and treatment monitoring.
- To discuss the advantages of newer PET ligands over existing methods like [18F]-fluorodeoxyglucose (FDG).
Main Methods:
- Evaluation of novel PET imaging ligands, including [18F]-fluorocellobiose.
- Assessment of ImmunoPET approaches targeting fungal cell wall components.
- Discussion of enzymatic synthesis and antibody engineering for PET ligand optimization.
Main Results:
- [18F]-fluorocellobiose demonstrates high specificity for live cellulolytic mold infections, including Aspergillus spp.
- Novel PET ligands show potential for accurate localization and differentiation of fungal infections.
- ImmunoPET offers a promising panfungal approach with potential for optimization.
Conclusions:
- New PET imaging ligands can overcome limitations of [18F]-FDG, improving diagnosis of invasive fungal infections.
- Accurate and rapid diagnosis using advanced PET tracers is crucial for patient outcomes.
- These advancements are significant for the vulnerable immunocompromised patient population.
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