Immature, but Not Mature, Dendritic Cells Are More Often Present in Aggressive Periodontitis Than Chronic Periodontitis: An Immunohistochemical Study

被引:11
|
作者
da Motta, Raphael J. G. [1 ]
Tirapelli, Camila [1 ]
da Silva, Roberto Juns [1 ]
Villafuerte, Kelly R. V. [2 ]
Almeida, Luciana Y. [3 ]
Ribeiro-Silva, Alfredo [4 ]
Leon, Jorge E. [5 ]
机构
[1] Univ Sao Paulo, Dept Dent Mat & Prosthodont, Ribeirao Preto, Brazil
[2] Univ Sao Paulo, Dept Oral & Maxillofacial Surg & Periodontol, Sao Paulo, Brazil
[3] Univ Estadual Paulista, Araraquara Dent Sch, Dept Diag & Surg, Sao Paulo, Brazil
[4] Univ Sao Paulo, Dept Pathol, Sao Paulo, Brazil
[5] Univ Sao Paulo, Dept Stomatol, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Aggressive periodontitis; immunology; oral pathology; LANGERHANS CELLS; IN-VIVO; GINGIVAL TISSUE; BONE LOSS; T-CELLS; LESIONS; DISEASE; INFLAMMATION; EXPRESSION; SUBPOPULATIONS;
D O I
10.1902/jop.2016.150729
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
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 > 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.
引用
收藏
页码:1499 / 1507
页数:9
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