PT  - JOURNAL ARTICLE
AU  - Jahandideh, Arghavan
AU  - Uotila, Sauli
AU  - Ståhle, Mia
AU  - Virta, Jenni
AU  - Li, Xiang-Guo
AU  - Kytö, Ville
AU  - Marjamäki, Päivi
AU  - Liljenbäck, Heidi
AU  - Taimen, Pekka
AU  - Oikonen, Vesa
AU  - Lehtonen, Jukka
AU  - Mäyränpää, Mikko I.
AU  - Chen, Qingshou
AU  - Low, Philip S.
AU  - Knuuti, Juhani
AU  - Roivainen, Anne
AU  - Saraste, Antti
TI  - Folate Receptor β–Targeted PET Imaging of Macrophages in Autoimmune Myocarditis
AID  - 10.2967/jnumed.119.241356
DP  - 2020 Nov 01
TA  - Journal of Nuclear Medicine
PG  - 1643--1649
VI  - 61
IP  - 11
4099  - http://jnm.snmjournals.org/content/61/11/1643.short
4100  - http://jnm.snmjournals.org/content/61/11/1643.full
SO  - J Nucl Med2020 Nov 01; 61
AB  - Currently available imaging techniques have limited specificity for the detection of active myocardial inflammation. Aluminum 18F-labeled 1,4,7-triazacyclononane-N,N′,N″-triacetic acid conjugated folate (18F-FOL) is a PET tracer targeting folate receptor β (FR-β), which is expressed on activated macrophages at sites of inflammation. We evaluated 18F-FOL PET for the detection of myocardial inflammation in rats with autoimmune myocarditis and studied the expression of FR-β in human cardiac sarcoidosis specimens. Methods: Myocarditis was induced by immunizing rats (n = 18) with porcine cardiac myosin in complete Freund adjuvant. Control rats (n = 6) were injected with Freund adjuvant alone. 18F-FOL was intravenously injected, followed by imaging with a small-animal PET/CT scanner and autoradiography. Contrast-enhanced high-resolution CT or 18F-FDG PET images were used for coregistration. Rat tissue sections and myocardial autopsy samples from 6 patients with cardiac sarcoidosis were studied for macrophages and FR-β. Results: The myocardium of 10 of 18 immunized rats showed focal macrophage-rich inflammatory lesions, with FR-β expression occurring mainly in M1-polarized macrophages. PET images showed focal myocardial 18F-FOL uptake colocalizing with inflammatory lesions (SUVmean, 2.1 ± 1.1), whereas uptake in the remote myocardium of immunized rats and controls was low (SUVmean, 0.4 ± 0.2 and 0.4 ± 0.1, respectively; P < 0.01). Ex vivo autoradiography of tissue sections confirmed uptake of 18F-FOL in myocardial inflammatory lesions. Uptake of 18F-FOL in inflamed myocardium was efficiently blocked by a nonlabeled FR-β ligand folate glucosamine in vivo. The myocardium of patients with cardiac sarcoidosis showed many FR-β–positive macrophages in inflammatory lesions. Conclusion: In a rat model of autoimmune myocarditis, 18F-FOL shows specific uptake in inflamed myocardium containing macrophages expressing FR-β, which were also present in human cardiac sarcoid lesions. Imaging of FR-β expression is a potential approach for the detection of active myocardial inflammation.