B-1a cells and plasma cells in periodontitis lesions

被引:25
作者
Donati, M. [1 ]
Liljenberg, B. [1 ]
Zitzmann, N. U. [1 ,2 ]
Berglundh, T. [1 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Dept Periodontol, SE-40530 Gothenburg, Sweden
[2] Univ Basel, Clin Periodontol Endodontol & Cariol, Sch Dent, Basel, Switzerland
关键词
inflammation; B lymphocytes; cell-surface molecules; autoimmunity; MEMBRANE-BOUND CD14; COLLAGEN TYPE-I; B-CELLS; ADULT PERIODONTITIS; T-CELLS; DISEASE; EXPRESSION; ANTIBODY; ANTIGEN; LIPOPOLYSACCHARIDE;
D O I
10.1111/j.1600-0765.2008.01178.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background and Objective: Host response mechanisms in periodontal tissues are complex and involve numerous systems of interactions between cells. The B-cell lineage seems to predominate in chronic periodontitis lesions. The aim of the present investigation was to study the correlation between inflammatory cells and some functional markers in gingival lesions obtained from subjects with severe chronic periodontitis. Material and Methods: Thirty-eight Caucasian subjects volunteered to take part in the study. A gingival biopsy from one randomly selected diseased proximal site (probing pocket depth > 6 mm and bleeding on probing positive) was obtained from each patient. Immunohistochemical preparation was used to identify inflammatory cells and functional markers. Correlations between the different percentages of cell markers were analyzed by pairwise correlation. Results: B cells (B-1a and B-2 cells) occurred in larger proportions than T cells and plasma cells. A statistically significant correlation was found between the percentage of B-1a cells and plasma cells and between all B lymphocytes and plasma cells. About 60% of B lymphocytes exhibited autoreactive features. Conclusion: It is suggested that B-1a cells constitute a significant part of the host response in periodontitis lesions and that plasma cells may develop from both B-2 and B-1a cells.
引用
收藏
页码:683 / 688
页数:6
相关论文
共 28 条
[1]   Presence of activated B-1 cells in chronic inflamed gingival tissue [J].
Aramaki, M ;
Nagasawa, T ;
Koseki, T ;
Ishikawa, I .
JOURNAL OF CLINICAL IMMUNOLOGY, 1998, 18 (06) :421-429
[2]   Aspects of adaptive host response in periodontitis [J].
Berglundh, T ;
Donati, M .
JOURNAL OF CLINICAL PERIODONTOLOGY, 2005, 32 :87-107
[3]   The presence of local and circulating autoreactive B cells in patients with advanced periodontitis [J].
Berglundh, T ;
Liljenberg, B ;
Tarkowski, A ;
Lindhe, J .
JOURNAL OF CLINICAL PERIODONTOLOGY, 2002, 29 (04) :281-286
[4]  
Bulut S, 2006, HEAD FACE MED, V2, P1
[5]  
Donati M, 2008, J PERIODONTOL, V79, P517, DOI [10.1902/jop.2008.070299, 10.1902/jop.2008.070299 ]
[6]   ANTIBODY TO COLLAGEN TYPE-I IN PERIODONTAL-DISEASE [J].
FTIS, A ;
SINGH, G ;
DOLBY, AE .
JOURNAL OF PERIODONTOLOGY, 1986, 57 (11) :693-698
[7]   Apoptosis in chronic adult periodontitis analyzed by in situ DNA breaks, electron microscopy, and immunohistochemistry [J].
Gamonal, J ;
Bascones, A ;
Acevedo, A ;
Blanco, E ;
Silva, A .
JOURNAL OF PERIODONTOLOGY, 2001, 72 (04) :517-525
[8]   Antigen-presenting cells in human periodontal disease tissues [J].
Gemmell, E ;
Carter, CL ;
Hart, DNJ ;
Drysdale, KE ;
Seymour, GJ .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2002, 17 (06) :388-393
[9]   Rh autoantigen presentation to helper T cells in chronic lymphocytic leukemia by malignant B cells [J].
Hall, AM ;
Vickers, MA ;
McLeod, E ;
Barker, RN .
BLOOD, 2005, 105 (05) :2007-2015
[10]   AUTOIMMUNITY TO COLLAGEN IN ADULT PERIODONTAL-DISEASE [J].
HIRSCH, HZ ;
TARKOWSKI, A ;
MILLER, EJ ;
GAY, S ;
KOOPMAN, WJ ;
MESTECKY, J .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1988, 17 (9-10) :456-459