Department of Periodontology, Faculty of Dentistry, Yuzuncu Yil University, Van, Turkey.
J Periodontal Res. 2013 Feb;48(1):44-51. doi: 10.1111/j.1600-0765.2012.01500.x. Epub 2012 Jul 19.
Cytokines produced by various cells are strong local mediators of inflammation. Mucosa-associated epithelial chemokine (CCL28), interleukin-8 (IL-8), interleukin-1beta (IL-1β) and tumor necrosis factor-alpha (TNF-α) are major cytokines that play important roles in the periodontal inflammatory process. In this study we aimed to compare the levels of CCL28, IL-8, IL-1β and TNF-α in the gingival crevicular fluid of both periodontally healthy subjects and in subjects diagnosed with gingivitis, chronic periodontitis and generalized aggressive periodontitis.
A total of 84 subjects participated in the study: 21 subjects had gingivitis, 21 subjects had chronic periodontitis, 21 subjects had generalized aggressive periodontitis and 21 were periodontally healthy. The levels of CCL28, IL-8, IL-1β and TNF-α were analyzed using enzyme-linked immune sorbent assay (ELISA).
The total levels of CCL28 and IL-8 in the gingival crevicular fluid of the generalized aggressive periodontitis group (324.74 ± 42.62 pg/30 s, 487.62 ± 49.21 pg/30 s) were significantly higher than those of the chronic periodontitis group (268.81 ± 28.64 pg/30 s, 423.65 ± 35.24 pg/30 s), the gingivitis group (146.35 ± 17.46 pg/30 s, 310.24 ± 48.20 pg/30 s) and the periodontally healthy group (92.46 ± 22.04 pg/30 s, 148.41 ± 24.64 pg/30 s). Similarly, the total levels of IL-1β and TNF-α in the generalized aggressive periodontitis group (110.23 ± 9.20 pg/30 s, 1284.46 ± 86.32 pg/30 s) were significantly higher than those in the chronic periodontitis group (423.65 ± 35.24 pg/30 s, 82.64 ± 9.12 pg/30 s), the gingivitis group (52.10 ± 7.15 pg/30 s, 824.24 ± 44.68 pg/30 s) and the periodontally healthy group (36.44 ± 8.86 pg/30 s, 628.26 ± 34.61 pg/30 s).
CCL28, IL-8, IL-1β and TNF-α may play key roles in the host response to inflammation in periodontal diseases. As the severity of periodontal diseases increases, destruction of periodontal tissues also increases. Inflammation is one among many factors that trigger periodontal tissue destruction. Identification of the mediators that influence the development and progression of inflammation in periodontal diseases may be very important in understanding the prognoses of periodontal diseases.
各种细胞产生的细胞因子是炎症的强烈局部介质。黏膜相关上皮趋化因子(CCL28)、白细胞介素-8(IL-8)、白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)是在牙周炎症过程中发挥重要作用的主要细胞因子。本研究旨在比较牙周健康受试者和诊断为牙龈炎、慢性牙周炎和广泛性侵袭性牙周炎受试者的龈沟液中 CCL28、IL-8、IL-1β 和 TNF-α 的水平。
共有 84 名受试者参加了这项研究:21 名受试者患有牙龈炎,21 名受试者患有慢性牙周炎,21 名受试者患有广泛性侵袭性牙周炎,21 名受试者牙周健康。使用酶联免疫吸附试验(ELISA)分析 CCL28、IL-8、IL-1β 和 TNF-α 的水平。
广泛性侵袭性牙周炎组龈沟液中 CCL28 和 IL-8 的总水平(324.74±42.62pg/30s,487.62±49.21pg/30s)明显高于慢性牙周炎组(268.81±28.64pg/30s,423.65±35.24pg/30s)、牙龈炎组(146.35±17.46pg/30s,310.24±48.20pg/30s)和牙周健康组(92.46±22.04pg/30s,148.41±24.64pg/30s)。同样,广泛性侵袭性牙周炎组中 IL-1β 和 TNF-α 的总水平(110.23±9.20pg/30s,1284.46±86.32pg/30s)明显高于慢性牙周炎组(423.65±35.24pg/30s,82.64±9.12pg/30s)、牙龈炎组(52.10±7.15pg/30s,824.24±44.68pg/30s)和牙周健康组(36.44±8.86pg/30s,628.26±34.61pg/30s)。
CCL28、IL-8、IL-1β 和 TNF-α 可能在牙周病宿主对炎症的反应中起关键作用。随着牙周病严重程度的增加,牙周组织的破坏也增加。炎症是触发牙周组织破坏的众多因素之一。鉴定影响牙周病炎症发生和进展的介质对于了解牙周病的预后可能非常重要。