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
相关论文
共 36 条
[1]   INTERLEUKIN-4 (IL-4) AND IL-6-PRODUCING MEMORY T-CELLS IN PERIPHERAL-BLOOD AND GINGIVAL TISSUES IN PERIODONTITIS PATIENTS WITH HIGH SERUM ANTIBODY-TITERS TO PORPHYROMONAS-GINGIVALIS [J].
AOYAGI, T ;
SUGAWARAAOYAGI, M ;
YAMAZAKI, K ;
HARA, K .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1995, 10 (05) :304-310
[2]   REVISITING AND REVISING SUPPRESSOR T-CELLS [J].
BLOOM, BR ;
SALGAME, P ;
DIAMOND, B .
IMMUNOLOGY TODAY, 1992, 13 (04) :131-136
[3]   Characterization of human skin-derived CD1a-positive lymph cells [J].
Brand, CU ;
Hunger, RE ;
Yawalkar, N ;
Gerber, HA ;
Schaffner, T ;
Braathen, LR .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1999, 291 (2-3) :65-72
[4]  
Chapple CC, 1998, J PATHOL, V186, P281
[5]   IDENTIFICATION OF LANGERHANS CELLS IN HUMAN GINGIVAL EPITHELIUM [J].
DIFRANCO, CF ;
TOTO, PD ;
ROWDEN, G ;
GARGIULO, AW ;
KEENE, JJ ;
CONNELLY, E .
JOURNAL OF PERIODONTOLOGY, 1985, 56 (01) :48-54
[6]   Isolation of human blood dendritic cells using the CMRF-44 monoclonal antibody: Implications for studies on antigen-presenting cell function and immunotherapy [J].
Fearnley, DB ;
McLellan, AD ;
Mannering, SI ;
Hock, BD ;
Hart, DNJ .
BLOOD, 1997, 89 (10) :3708-3716
[7]   ADHESION MOLECULE EXPRESSION IN CHRONIC INFLAMMATORY PERIODONTAL-DISEASE TISSUE [J].
GEMMELL, E ;
WALSH, LJ ;
SAVAGE, NW ;
SEYMOUR, GJ .
JOURNAL OF PERIODONTAL RESEARCH, 1994, 29 (01) :46-53
[8]   PHENOTYPIC ANALYSIS OF B-CELLS EXTRACTED FROM HUMAN PERIODONTAL-DISEASE TISSUE [J].
GEMMELL, E ;
SEYMOUR, GJ .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1991, 6 (06) :356-362
[9]  
GEMMELL E, 2000, J PERIODONTAL RES, V35, P1
[10]  
HOCK BD, 1994, IMMUNOLOGY, V83, P573