Cytokine production by oral and peripheral blood neutrophils in adult periodontitis

被引:39
作者
Galbraith, GMP [1 ]
Hagan, C [1 ]
Steed, RB [1 ]
Sanders, JJ [1 ]
Javed, T [1 ]
机构
[1] MED UNIV S CAROLINA,DEPT STOMATOL,CHARLESTON,SC 29425
关键词
neutrophils; interleukin-1; beta; tumor necrosis factor-alpha; bone resorption; periodontitis/pathogens;
D O I
10.1902/jop.1997.68.9.832
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
PROINFLAMMATORY CYTOKINES SUCH AS tumor necrosis factor-alpha (TNF-alpha) and interleukin 1 beta (IL-1 beta) also possess bone-resorptive properties, and are generally considered to play a role in the pathogenesis of periodontal disease. In the present study, TNF-alpha and IL-1 beta production by oral and peripheral blood polymorphonuclear leukocytes (PMN) was examined in 40 patients with adult periodontitis and 40 orally healthy matched controls. Oral PMN released considerable amounts of both cytokines in unstimulated culture, and there was no difference between patients and controls when the cytokine levels were corrected for cell number, However, when the effect of disease activity was examined, cytokine release by oral PMN was found to be greatest in patients with advanced periodontitis. Within the healthy control group, IL-1 beta production by oral PMN was significantly higher in males (Mann-Whitney rest, P = 0.0008). Examination of IL-1 beta production by peripheral blood PMN exposed to recombinant human granulocyte-macrophage colony stimulating factor revealed no difference between the patient and control groups. In contrast, IL-1 beta production by peripheral blood PMN was significantly reduced in patients with advanced disease (Mann-Whitney test, P = 0.02), and peripheral PMN IL-1 beta synthesis was greater in female controls (Mann-Whitney test, P = 0.054). No effect of race on cytokine production could be discerned in patients or controls. These results indicate that several factors influence cytokine production in oral health and disease, and that a dichotomy in cytokine gene expression exists between oral and peripheral blood PMN in adult periodontitis.
引用
收藏
页码:832 / 838
页数:7
相关论文
共 41 条
[1]   SYNTHESIS OF PROINFLAMMATORY CYTOKINES BY HUMAN GINGIVAL FIBROBLASTS IN RESPONSE TO LIPOPOLYSACCHARIDES AND INTERLEUKIN-1-BETA [J].
AGARWAL, S ;
BARAN, C ;
PIESCO, NP ;
QUINTERO, JC ;
LANGKAMP, HH ;
JOHNS, LP ;
CHANDRA, CS .
JOURNAL OF PERIODONTAL RESEARCH, 1995, 30 (06) :382-389
[2]  
*AM AC PER, 1991, CURR PROC TERM, P15
[3]   Periodontal status in the United States, 1988-91: Prevalence, extent and demographic variation [J].
Brown, LJ ;
Brunelle, JA ;
Kingman, A .
JOURNAL OF DENTAL RESEARCH, 1996, 75 :672-683
[4]  
DeNardin E, 1996, J PERIODONTOL, V67, P345, DOI 10.1902/jop.1996.67.3s.345
[5]   INFLAMMATORY MEDIATORS AND IMMUNOGLOBULINS IN GCF FROM HEALTHY, GINGIVITIS AND PERIODONTITIS SITES [J].
EBERSOLE, JL ;
SINGER, RE ;
STEFFENSEN, B ;
FILLOON, T ;
KORNMAN, KS .
JOURNAL OF PERIODONTAL RESEARCH, 1993, 28 (06) :543-546
[6]   Transcriptional and post-transcriptional regulation of GM-CSF-induced IL-1 beta gene expression in PMN [J].
Fernandez, MC ;
Walters, J ;
Marucha, P .
JOURNAL OF LEUKOCYTE BIOLOGY, 1996, 59 (04) :598-603
[7]  
GALBRAITH GMP, 1988, AM J PATHOL, V133, P347
[8]  
Genco R J, 1993, Periodontol 2000, V2, P98, DOI 10.1111/j.1600-0757.1993.tb00223.x
[9]   NEUTROPHIL DEFECTS AS RISK-FACTORS FOR PERIODONTAL-DISEASES [J].
HART, TC ;
SHAPIRA, L ;
VANDYKE, TE .
JOURNAL OF PERIODONTOLOGY, 1994, 65 (05) :521-529
[10]  
HAZIOT A, 1993, J IMMUNOL, V150, P5556