Folate Receptor β-Targeted PET Imaging of Macrophages in Autoimmune Myocarditis.

Abstract

Currently available imaging techniques have limited specificity for the detection of active myocardial inflammation. Aluminum ¹⁸F-labeled 1,4,7-triazacyclononane-<i>N,N',N″</i>-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. <b>Methods:</b> Myocarditis was induced by immunizing rats (<i>n</i> = 18) with porcine cardiac myosin in complete Freund adjuvant. Control rats (<i>n</i> = 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. <b>Results:</b> 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 (SUV_mean, 2.1 ± 1.1), whereas uptake in the remote myocardium of immunized rats and controls was low (SUV_mean, 0.4 ± 0.2 and 0.4 ± 0.1, respectively; <i>P</i> < 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. <b>Conclusion:</b> 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.