ABSTRACT
Objective: Central giant cell lesions (CGCL) and peripheral giant cell lesions (PGCL) occur in the jaws and containosteoclast-like giant cells and mononuclear cells positive for the macrophage marker CD68. The participationof immune-inflammatory mechanisms has been proposed in the lesions development. As IL-10 is one of the mostimportant anti-inflammatory cytokines and it is also an inhibitory cytokine to macrophage function and boneresorption, the purpose of the present study was to investigate its expression together with its receptor (IL-10Rα)in CGCL and PGCL.Study Design: Six fragments of CGCL and seven fragments of PGCL were obtained by surgical excision. Frozenspecimens were cut and subjected to immunofluorescence staining using fluorescent-labeled anti-CD68, anti-IL-10, and anti-IL-10Rα monoclonal antibodies. Microscopic analyses were performed and the percentage of positivemononuclear and giant cells for each parameter was obtained.Results: Our results revealed that all giant cells from CGCL and PGCL were CD68+ and IL-10Rα+ and that themajority was also positive for IL-10. More than 50% of the mononuclear cells from both lesions expressed IL-10Rα and the majority of these cells were CD68+ and IL-10+.Conclusion: Considering that IL-10 has inhibitory effects on the pathologic processes related to the developmentof the oral giant cell lesions, the high frequencies of cells producing this cytokine seems contradictory to theselesions growth. Investigation about the production of inflammatory cytokines as well as the IL-10 signaling pathwaysin oral giant cell lesions is required to elucidate the immunopathology of CGCL and PGCL (AU)
