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Folate Receptor β Targeted PET Imaging of Macrophages in Autoimmune Myocarditis

Xiang-Guo Li; Vesa Oikonen; Antti Saraste; Arghavan Jahandideh; Anne Roivainen; Philip S. Low; Juhani Knuuti; Jukka Lehtonen; Ville Kytö; Jenni Virta; Qingshou Chen; Mikko I. Mäyranpää; Päivi Marjamäki; Pekka Taimen; Sauli Uotila; Heidi Liljenbäck; Mia Ståhle

Folate Receptor β Targeted PET Imaging of Macrophages in Autoimmune Myocarditis

Xiang-Guo Li
Vesa Oikonen
Antti Saraste
Arghavan Jahandideh
Anne Roivainen
Philip S. Low
Juhani Knuuti
Jukka Lehtonen
Ville Kytö
Jenni Virta
Qingshou Chen
Mikko I. Mäyranpää
Päivi Marjamäki
Pekka Taimen
Sauli Uotila
Heidi Liljenbäck
Mia Ståhle
Katso/Avaa
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SOC NUCLEAR MEDICINE INC
doi:10.2967/jnumed.119.241356
URI
http://jnm.snmjournals.org/content/early/2020/04/10/jnumed.119.241356.abstract
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042825959
Tiivistelmä

Rationale: Currently available imaging techniques have limited specificity for the detection of active myocardial inflammation. Aluminum fluoride-18-labeled 1,4,7-triazacyclononane-N,N′,N″-triacetic acid conjugated folate (18F-FOL) is a positron emission tomography (PET) tracer targeting folate receptor β (FR-β) that 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 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’s adjuvant. Control rats (n = 6) were injected with Freund’s adjuvant alone. 18F-FOL was intravenously injected followed by imaging with a small animal PET/computed tomography (CT) scanner and autoradiography. Contrast-enhanced high-resolution CT or 2-deoxy-2-18F-fluoro-D-glucose (18F-FDG) PET images were used for co-registration. Rat tissue sections and myocardial autopsy samples of 6 patients with cardiac sarcoidosis were studied for macrophages and FR-β. 

Results: The myocardium of 10 out 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 co-localizing 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 to inflamed myocardium was efficiently blocked by a non-labeled 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.

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