TY - JOUR
T1 - Immature, but not mature, dendritic cells are more often present in aggressive periodontitis than chronic periodontitis
T2 - An immunohistochemical study
AU - Da Motta, Raphael J.G.
AU - Tirapelli, Camila
AU - Da Silva, Roberto Juns
AU - Villafuerte, Kelly R.V.
AU - Almeida, Luciana Y.
AU - Ribeiro-Silva, Alfredo
AU - León, Jorge E.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Background: Dendritic cells (DCs) form a key link between innate and adaptive immune responses. The aim of this study is to analyze presence and distribution of immature (im) and mature (m) DCs in gingival tissue samples obtained from patients diagnosed with aggressive periodontitis (AgP), chronic periodontitis (CP), and clinically healthy periodontium (control group). Methods: Gingival tissue samples obtained from patients with: 1) AgP (aged <35 years); 2) CP (aged ≤35 years); and 3) control group (aged 7gt;18 years) (n = 10 per group) were collected. Two-way analysis of variance and posterior Fisher least significant difference test were used to observe differences between the means of cells positively marked for imDC (S100, CD1a, and CD207) and mDC (CD208) immunomarkers. Results: imDCs were more numerous in AgP than CP and control groups, being statistically significant only for S100+ cells. Conversely, mDCs were visualized in higher numbers in CP than AgP and control groups (both P <0.05). Considering frequency of immunostained cells, the number of S100+ cells was greater than CD207+ and CD1a+ cells, followed by a lesser number of CD208+ cells, in all groups. Conclusions: Considering that the ability of DCs to regulate immunity is dependent on DC maturation, results suggest that predominance of imDCs appears to be involved in AgP pathogenesis, probably due to lack of ability to induce immune cell activation. Further studies are necessary to elucidate the role of DC maturation in regulating immune responses in periodontal disease.
AB - Background: Dendritic cells (DCs) form a key link between innate and adaptive immune responses. The aim of this study is to analyze presence and distribution of immature (im) and mature (m) DCs in gingival tissue samples obtained from patients diagnosed with aggressive periodontitis (AgP), chronic periodontitis (CP), and clinically healthy periodontium (control group). Methods: Gingival tissue samples obtained from patients with: 1) AgP (aged <35 years); 2) CP (aged ≤35 years); and 3) control group (aged 7gt;18 years) (n = 10 per group) were collected. Two-way analysis of variance and posterior Fisher least significant difference test were used to observe differences between the means of cells positively marked for imDC (S100, CD1a, and CD207) and mDC (CD208) immunomarkers. Results: imDCs were more numerous in AgP than CP and control groups, being statistically significant only for S100+ cells. Conversely, mDCs were visualized in higher numbers in CP than AgP and control groups (both P <0.05). Considering frequency of immunostained cells, the number of S100+ cells was greater than CD207+ and CD1a+ cells, followed by a lesser number of CD208+ cells, in all groups. Conclusions: Considering that the ability of DCs to regulate immunity is dependent on DC maturation, results suggest that predominance of imDCs appears to be involved in AgP pathogenesis, probably due to lack of ability to induce immune cell activation. Further studies are necessary to elucidate the role of DC maturation in regulating immune responses in periodontal disease.
KW - Aggressive periodontitis
KW - Immunology
KW - Oral pathology
UR - https://www.scopus.com/pages/publications/84997770114
U2 - 10.1902/jop.2016.150729
DO - 10.1902/jop.2016.150729
M3 - Article
C2 - 27389962
AN - SCOPUS:84997770114
SN - 0022-3492
VL - 87
SP - 1499
EP - 1507
JO - Journal of Periodontology
JF - Journal of Periodontology
IS - 12
ER -