LAUSR

BACKGROUND Persistent host immune responses initiated by oral bacteria protect host against infection but may also elicit the process of sustained periodontal inflammation and subsequent alveolar bone loss. Interleukin-10 (IL-10), an anti-inflammatory cytokine, can downregulate pro-inflammatory cytokine and inhibit neutrophil migration in inflammation. IL-10-expressing regulatory B cells (B10) is termed by negatively regulating immune response through IL-10 and are mainly restricted in CD19+ CD1dhi CD5+ B cells in mice. Our current study was aimed to explore the effect of locally transferred CD19+ CD1dhi CD5+ B cells on inflammation and alveolar bone loss in an experimental periodontitis mouse model. METHODS Ligation plus P. gingivalis (Pg) infection was used to induce periodontitis in a mouse model. CD19+ CD1dhi CD5+ B cells were sorted by flow cytometry and transferred into the gingivae immediately on the fifth day after ligation. All the mice were sacrificed on day 14 after ligation. RESULTS H&E staining showed that inflammatory cell infiltration was significantly reduced by the CD19+ CD1dhi CD5+ B cells. Toluidine blue staining showed that the CD19+ CD1dhi CD5+ B cells alleviated alveolar bone loss in the ligature/Pg-induced periodontitis in mice. Immunohistochemical staining showed Receptor Activator of NF-KappaB Ligand (RANKL), Interleukin-1β(IL-1β) and Interleukin-17 (IL-17) were decreased after the CD19+ CD1dhi CD5+ B cell transfer. Immunofluorescent staining showed that IL-10 was increased while the number of Ly6G+ neutrophil and its RANKL production were decreased in gingival tissue. CONCLUSIONS These results indicated that locally transferred CD19+ CD1dhi CD5+ B cells may alleviate alveolar bone loss through inhibiting pro-inflammatory cytokine expression and RANKL-expressing neutrophils in the periodontitis mouse model. This article is protected by copyright. All rights reserved.