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Macrophage Activity in Infected Areas of an Experimental Vertebral Osteomyelitis Model: USPIO-enhanced MR Imaging—Feasibility Study¹

¹ From the Departments of Radiology 2 (G.B., J.L.D., S.K.) and Bacteriology (F.J., G.P.), University Hospital of Strasbourg, Strasbourg, France; EA 3432 (G.B., F.J., G.P., J.L.D., S.K.), Institute of Histology, Faculty of Medicine (N.B.), and INSERM U666 (N.B.), University Louis Pasteur, Strasbourg, France; Guerbet Research, Aulnay-sous-Bois, France (P.R.); and Department of Neuroradiology, University Hospital of Nantes, Nantes, France (H.D.). Received July 19, 2007; revision requested September 20; revision received December 2; accepted January 28, 2008; final version accepted January 31. Address correspondence to G.B., Department of Radiology 2, University Hospital, Hautepierre Hospital, Avenue Molière, 67098 Strasbourg, France (e-mail: guillaume.bierry{at}chru-strasbourg.fr).

Purpose: To prospectively evaluate ultrasmall superparamagnetic iron oxide (USPIO) magnetic resonance (MR) imaging for the depiction of macrophages in infected areas of an experimental rabbit vertebral osteomyelitis model.

Materials and Methods: Lumbar vertebral osteomyelitis was induced in 10 rabbits with intradiscal injection of bacteria in a vertebral disk (test level) versus saline injection in another disk (control level). After a mean interval of 12 days, rabbits were imaged prior to and 24 hours after administration of USPIO. The MR imaging protocol included T1-weighted spin-echo, T2-weighted fast spin-echo, and T2*-weighted gradient-echo sequences. MR findings were compared with histologic findings (macrophage immunostaining and Perls Prussian blue staining). A Wilcoxon signed rank test was used to compare signal-to-noise ratio (SNR) results before and after USPIO administration.

Results: T1-weighted MR images of infected vertebral test levels obtained 24 hours after USPIO administration showed a significant increase in SNR (P = .005), whereas T2- and T2*-weighted images showed no significant changes in SNR (P = .14 and P = .87, respectively). Histologic examination results of infected areas demonstrated complete replacement of hematopoietic bone marrow by macrophage infiltration. Perls Prussian blue staining showed that some macrophages were iron loaded. T1- (P = .02), T2- (P = .04), and T2*-weighted (P = .04) images of control vertebrae showed a significant decrease in SNR. Histologic examination results confirmed the persistence of normal hematopoietic bone marrow without macrophage infiltration, which was reflected by more intensive Perls Prussian blue staining compared with that in infected areas.

Conclusion: MR imaging can depict USPIO-loaded macrophage infiltration present in infected areas in an experimental rabbit model of vertebral osteomyelitis.

© RSNA, 2008

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