Innate immune system is implicated in recurrent aphthous ulcer pathogenesis

被引:65
作者
Lewkowicz, N
Lewkowicz, P
Kurnatowska, A
Banasik, M
Glowacka, E
Cedzynski, M
Swierzko, A
Lauk-Puchala, B
Tchórzewski, H
机构
[1] Med Univ Lodz, Dept Oral Mucosal & Periodontal Dis, PL-92213 Lodz, Poland
[2] Inst Polish Mothers Mem Hosp, Dept Clin Immunol, PL-93338 Lodz, Poland
[3] Polish Acad Sci, Dept Infect Immunol, Microbiol & Virol Ctr, PL-93232 Lodz, Poland
关键词
innate immunity; recurrent aphthous ulcers;
D O I
10.1034/j.1600-0714.2003.00181.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: Recurrent aphthous ulcers (RAU) is a chronic inflammatory disease with evidence of inappropriate immune response. This study presents the status of innate immune system in RAU. Methods: Twenty RAU patients and 19 healthy individuals were selected. The status of peripheral blood neutrophils (reactive oxygen intermediates (ROI) production, CD11b, TNF-RI and TNF-RII expression), concentration of antioxidants, sTNF-R, C3c, C4 and haemolytic activity of the complement system, as well as mannose-binding lectin (MBL), in the serum of RAU patients in active stage and in remission of the disease were determined. Results: Peripheral blood neutrophils were primed in RAU, which resulted in increased ROI production by resting and fMLP-stimulated neutrophils and diminished ROI production after in vitro priming. The increased expression of CD11b on resting and fMLP-stimulated neutrophils in RAU may also point to their previous in vivo stimulation. The decreased total antioxidant status of serum observed in RAU may be a result of increased ROI production by peripheral blood neutrophils. The levels of C3c, C4 and haemolytic activity of the complement system were higher in RAU than in healthy people. No significant differences between active and remission RAU were noted. Conclusion: Presented observations confirm that the innate immune system is involved in RAU pathogenesis.
引用
收藏
页码:475 / 481
页数:7
相关论文
共 31 条
[1]   Tumor necrosis factor-alpha and FMLP receptors are functionally linked during FMLP-stimulated activation of adherent human neutrophils [J].
Balazovich, KJ ;
Suchard, SJ ;
Remick, DG ;
Boxer, LA .
BLOOD, 1996, 88 (02) :690-696
[2]  
BEMELMANS MHA, 1993, J IMMUNOL, V151, P5554
[3]   Elevated levels of interferon gamma, tumor necrosis factor α, interleukins 2, 4, and 5, but not interleukin 10, are present in recurrent aphthous stomatitis [J].
Buño, IJ ;
Huff, C ;
Weston, WL ;
Cook, DT ;
Brice, SL .
ARCHIVES OF DERMATOLOGY, 1998, 134 (07) :827-831
[4]  
CEDZYNSKI M, 2000, CTR EUR J IMMUNOL, V25, P1
[5]   Neutrophil priming: pathophysiological consequences and underlying mechanisms [J].
Condliffe, AM ;
Kitchen, E ;
Chilvers, ER .
CLINICAL SCIENCE, 1998, 94 (05) :461-471
[6]   SPONTANEOUS MIGRATION AND CHEMOTACTIC ACTIVITY OF NEUTROPHIL POLYMORPHONUCLEAR LEUKOCYTES IN RECURRENT APHTHOUS ULCERATION [J].
DAGALIS, P ;
BAGG, J ;
WALKER, DM .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1987, 64 (03) :298-301
[7]   Respiratory burst in human neutrophils [J].
Dahlgren, C ;
Karlsson, A .
JOURNAL OF IMMUNOLOGICAL METHODS, 1999, 232 (1-2) :3-14
[8]  
HASAN A, 1995, CLIN EXP IMMUNOL, V99, P392
[9]  
Healy CM, 1999, J ORAL PATHOL MED, V28, P5
[10]   Raised levels of circulating VCAM-1 and circulating E-selectin in patients with recurrent oral ulceration [J].
Healy, CM ;
Enobakhare, B ;
Haskard, DO ;
Thornhill, MH .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1997, 26 (01) :23-28