Journal
CLINICAL ORAL INVESTIGATIONS
Volume 25, Issue 4, Pages 2335-2344Publisher
SPRINGER HEIDELBERG
DOI: 10.1007/s00784-020-03556-2
Keywords
Biopsy; Dental implant; Immunohistochemistry; Peri-implantitis; Macrophage polarization
Categories
Funding
- Projekt DEAL
- Department of Oral Surgery and Implantology, Carolinum, Johann Wolfgang Goethe-University Frankfurt, Frankfurt, Germany
- Osteology Foundation Scholarship Grant, Lucerne, Switzerland
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The study immunohistochemically characterized macrophage polarization at peri-implantitis sites and found that macrophages constituted a significant portion of the inflammatory cellular composition, with a higher expression of M1 phenotype in advanced peri-implantitis cases. This higher M1 expression may play a critical role in disease progression.
Objectives To immunohistochemically characterize and correlate macrophage M1/M2 polarization status with disease severity at peri-implantitis sites. Materials and methods A total of twenty patients (n = 20 implants) diagnosed with peri-implantitis (i.e., bleeding on probing with or without suppuration, probing depths >= 6 mm, and radiographic marginal bone loss >= 3 mm) were included. The severity of peri-implantitis was classified according to established criteria (i.e., slight, moderate, and advanced). Granulation tissue biopsies were obtained during surgical therapy and prepared for immunohistological assessment and macrophage polarization characterization. Macrophages, M1, and M2 phenotypes were identified through immunohistochemical markers (i.e., CD68, CD80, and CD206) and quantified through histomorphometrical analyses. Results Macrophages exhibiting a positive CD68 expression occupied a mean proportion of 14.36% (95% CI 11.4-17.2) of the inflammatory connective tissue (ICT) area. Positive M1 (CD80) and M2 (CD206) macrophages occupied a mean value of 7.07% (95% CI 5.9-9.4) and 5.22% (95% CI 3.8-6.6) of the ICT, respectively. The mean M1/M2 ratio was 1.56 (95% CI 1-12-1.9). Advanced peri-implantitis cases expressed a significantly higher M1 (%) when compared with M2 (%) expression. There was a significant correlation between CD68 (%) and M1 (%) expression and probing depth (PD) values. Conclusion The present immunohistochemical analysis suggests that macrophages constitute a considerable proportion of the inflammatory cellular composition at peri-implantitis sites, revealing a significant higher expression for M1 inflammatory phenotype at advanced peri-implantitis sites, which could possibly play a critical role in disease progression.
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