4.7 Article

[68Ga]Ga-FAPI-46 PET for non-invasive detection of pulmonary fibrosis disease activity

Journal

Publisher

SPRINGER
DOI: 10.1007/s00259-022-05814-9

Keywords

Fibroblast activation protein; Idiopathic; Pulmonary fibrosis; Positron emission tomography imaging; [Ga-68] Ga-FAPI-46

Funding

  1. Cancer Center Support Grant NCI [P30CA014520]
  2. UW Department of Pathology and Laboratory Medicine, UWCCC [P30 CA014520]
  3. Office of The Director- NIH [S10 OD023526]

Ask authors/readers for more resources

The utility of fibroblast activation protein inhibitor for positron emission tomography (FAPI PET) imaging in monitoring lung fibrosis activity was determined in a mouse model. FAPI PET was able to detect the presence and activity of lung fibrogenesis, providing a promising tool for assessing disease activity and evaluating therapeutic interventions.
Purpose The lack of effective molecular biomarkers to monitor idiopathic pulmonary fibrosis (IPF) activity or treatment response remains an unmet clinical need. Herein, we determined the utility of fibroblast activation protein inhibitor for positron emission tomography (FAPI PET) imaging in a mouse model of pulmonary fibrosis. Methods Pulmonary fibrosis was induced by intratracheal administration of bleomycin (1 U/kg) while intratracheal saline was administered to control mice. Subgroups from each cohort (n = 3-5) underwent dynamic 1 h PET/CT after intravenously injecting FAPI-46 radiolabeled with gallium-68 ([Ga-68]Ga-FAPI-46) at 7 days and 14 days following disease induction. Animals were sacrificed following imaging for ex vivo gamma counting and histologic correlation. [Ga-68]Ga-FAPI-46 uptake was quantified and reported as percent injected activity per cc (%IA/cc) or percent injected activity (%IA). Lung CT density in Hounsfield units (HU) was also correlated with histologic examinations of lung fibrosis. Results CT only detected differences in the fibrotic response at 14 days post-bleomycin administration. [Ga-68]Ga-FAPI-46 lung uptake was significantly higher in the bleomycin group than in control subjects at 7 days and 14 days. Significantly (P = 0.0012) increased [Ga-68]Ga-FAPI-46 lung uptake in the bleomycin groups at 14 days (1.01 +/- 0.12%IA/cc) vs. 7 days (0.33 +/- 0.09%IA/cc) at 60 min post-injection of the tracer was observed. These findings were consistent with an increase in both fibrinogenesis and FAP expression as seen in histology. Conclusion CT was unable to assess disease activity in a murine model of IPF. Conversely, FAPI PET detected both the presence and activity of lung fibrogenesis, making it a promising tool for assessing early disease activity and evaluating the efficacy of therapeutic interventions in lung fibrosis patients.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available