Our previous study demonstrated that
IL-10 secreting B (B10) cells alleviate
inflammation and bone loss in experimental
periodontitis. The purpose of this study is to determine whether
antigen-specificity is required for the local infiltration of B10 cells. Experimental
periodontitis was induced in the recipient mice by placement of
silk ligature with or without the presence of live Porphyromonas gingivalis (P. gingivalis). Donor mice were pre-immunized by intraperitoneal (IP) injection of
formalin-fixed P. gingivalis, or PBS as non-immunized control. Spleen B cells were purified and treated with LPS and CpG for 48 h to expand the B10 population in vitro. Fluorescence-labelled B10 cells were transferred into the recipient mice by tail vein injection and were tracked on day 0, 3, 5 and 10 using IVIS Spectrum in vivo imaging system. The number of B10 cells and P. gingivalis-binding B cells were significantly increased after in vitro treatment of LPS and CpG. On day 5, the fluorescence intensity in gingival tissues was the highest in mice transferred with B10 cells from pre-immunized donor mice. Gingival expression of
IL-6, TNF-α, RANKL/OPG ratio and
periodontal bone loss in recipient mice were significantly reduced, and the expression of
IL-10 and the number of CD19+ B cells were significantly increased after pre-immunized B10 cell transfer in the presence of
antigen, compared to those with non-immunized B10 cell transfer or no
antigen presence. This study suggests that
antigen specificity dictate the local infiltration of B10 cells into periodontal tissue and these
antigen-specific B10 cells promote anti-inflammatory responses.