Imaging of inflammatory cellular protagonists in human atherosclerosis: a dual-isotope SPECT approach.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32291511.
- Also identified by DOI 10.1007/s00259-020-04776-0 and PMC identifier 7567726.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Atherosclerotic plaque development and progression signifies a complex inflammatory disease mediated by a multitude of proinflammatory leukocyte subsets. Using single photon emission computed tomography (SPECT) coupled with computed tomography (CT), this study tested a new dual-isotope acquisition protocol to assess each radiotracer's capability to identify plaque phenotype and inflammation levels pertaining to leukocytes expressing leukocyte function-associated antigen-1 (LFA-1) and the leukocyte subset of proinflammatory macrophages expressing somatostatin receptor subtype-2 (SST<sub>2</sub>). Individual radiotracer uptake was quantified and the presence of corresponding immunohistological cell markers was assessed. Human symptomatic carotid plaque segments were obtained from endarterectomy. Segments were incubated in dual-isotope radiotracers [<sup>111</sup>In]In-DOTA-butylamino-NorBIRT ([<sup>111</sup>In]In-Danbirt) and [<sup>99m</sup>Tc]Tc-[N<sup>0-1</sup><sub>4</sub>,Asp<sup>0</sup>,Tyr<sup>3</sup>]-octreotate ([<sup>99m</sup>Tc]Tc-Demotate 2) before scanning with SPECT/CT. Plaque phenotype was classified as pathological intimal thickening, fibrous cap atheroma or fibrocalcific using histology sections based on distinct morphological characteristics. Plaque segments were subsequently immuno-stained with LFA-1 and SST<sub>2</sub> and quantified in terms of positive area fraction and compared against the corresponding SPECT images. Focal uptake of co-localising dual-radiotracers identified the heterogeneous distribution of inflamed regions in the plaques which co-localised with positive immuno-stained regions of LFA-1 and SST<sub>2</sub>. [<sup>111</sup>In]In-Danbirt and [<sup>99m</sup>Tc]Tc-Demotate 2 uptake demonstrated a significant positive correlation (r = 0.651; p = 0.001). Fibrous cap atheroma plaque phenotype correlated with the highest [<sup>111</sup>In]In-Danbirt and [<sup>99m</sup>Tc]Tc-Demotate 2 uptake compared with fibrocalcific plaques and pathological intimal thickening phenotypes, in line with the immunohistological analyses. A dual-isotope acquisition protocol permits the imaging of multiple leukocyte subsets and the pro-inflammatory macrophages simultaneously in atherosclerotic plaque tissue. [<sup>111</sup>In]In-Danbirt may have added value for assessing the total inflammation levels in atherosclerotic plaques in addition to classifying plaque phenotype.
Medical subject headings
- Atherosclerosis
- Plaque, Atherosclerotic