Antigen-presenting cells in human periodontal disease tissues

被引:44
作者
Gemmell, E [1 ]
Carter, CL
Hart, DNJ
Drysdale, KE
Seymour, GJ
机构
[1] Univ Queensland, Sch Dent, Brisbane, Qld 4072, Australia
[2] Mat Med Res Inst, Brisbane, Australia
来源
ORAL MICROBIOLOGY AND IMMUNOLOGY | 2002年 / 17卷 / 06期
关键词
antigen-presenting cells; B cells; dendritic cells; macrophages; periodontal disease;
D O I
10.1034/j.1399-302X.2002.170609.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
T cells are present in the inflammatory infiltrates of periodontal disease lesions and require antigen presentation by antigen-presenting cells (APCs). While it is still not known whether Th1 or Th2 cells predominate in these lesions, it has been reported that different APCs may induce activation of different T-cell subsets. An immunoperoxidase technique was used to investigate the presence of CD1a+, CMRF-44+, CMRF-58+ and CD83+ dendritic cells, CD14+ macrophages or dendritic cell precursors and CD19+ B cells in gingival biopsies from 21 healthy or gingivitis and 25 periodontitis subjects. The samples were divided into three groups according to the size of infiltrate (group 1, small infiltrates; group 2, medium infiltrates; group 3, extensive infiltrates). The presence of numerous CD1a+ Langerhans cells was noted in the epithelium with no differences between the healthy/gingivitis and periodontitis groups. The percentage of CD83+ dendritic cells in the infiltrates was higher than the percentage of CD1a+, CMRF-44+ or CMRF-58+ dendritic cells. Endothelial cells positive for CD83 were found predominantly in areas adjacent to infiltrating cells, CD83+ dendritic cells being noted in the region of CD83+ endothelium. The percentage of CD14+ cells in the inflammatory infiltrates was similar to that of CD83+ dendritic cells. B cells were the predominant APC in group 2 and 3 tissues. The percentage of B cells in group 3 periodontitis lesions was increased in comparison with group 1 periodontitis tissues and also in comparison with group 3 healthy/gingivitis sections. Functional studies are required to determine the roles of different APC subpopulations in periodontal disease.
引用
收藏
页码:388 / 393
页数:6
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